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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Hematologic malignancies constitute a group of neoplasms with extremely heterogeneous clinical and behavioral characteristics that lead to aggressive or indolent&#44; acute or chronic conditions&#44; with different prognoses and involvement of different organs&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> The skin may be involved in a specific way&#44; through infiltration by malignant cells&#44; or non-specific&#44; as in paraneoplastic dermatoses&#44; in alterations common to hematological disorders&#44; such as pallor and ecchymosis&#44; among others&#44; and as those related to treatment and opportunistic infections&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;2</span></a> Cutaneous involvement substantially impacts the quality of life of the hematologic patient&#44; in addition to compromising the prognosis in different cases&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">Specific skin lesions secondary to systemic hematologic malignancy infiltration &#40;Part 1&#41; and the most common paraneoplastic skin diseases associated with hematologic systemic neoplasms &#40;Part 2&#41; will be discussed&#46; Primary cutaneous lymphomas will not be addressed&#46; <a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a> briefly describes the reviewed conditions and their treatment and Table 2 the epidemiological data of these conditions&#44; according to the literature&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><elsevierMultimedia ident="tbl0010"></elsevierMultimedia></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Specific skin lesions secondary to systemic hematologic malignancy infiltration</span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Leukemia cutis</span><p id="par0015" class="elsevierStylePara elsevierViewall">Leukemias are neoplastic proliferations of leukocytes and their precursors in the bone marrow and peripheral blood&#46;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;4</span></a> They are myeloid or lymphoid in origin and&#44; according to cell maturation&#44; acute or chronic&#46;<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">5&#44;6</span></a> Leukemia cutis &#40;LC&#41; is the extramedullary cutaneous manifestation caused by the infiltration of leukemic cells into the epidermis&#44; dermis&#44; or subcutaneous tissue&#46;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;7</span></a> It appears before&#44; during&#44; or after the manifestation of the systemic disease as an extramedullary occurrence of the initial disease&#44; as the first manifestation of the hematologic disease&#44; or&#44; rarely&#44; as the primary disease&#46; <a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">7&#44;8</span></a> The rare cases that occur before bone marrow or peripheral blood involvement&#44; whose systemic involvement may take months to years to appear&#44; are called aleukemic leukemias&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">9&#44;10</span></a></p><p id="par0020" class="elsevierStylePara elsevierViewall">Leukemia cutis most frequently affects individuals with acute myeloid leukemia &#40;AML&#41;&#59; however&#44; it is also seen in chronic myeloid leukemia &#40;CML&#41;&#44; acute lymphocytic leukemia &#40;ALL&#41;&#44; chronic lymphocytic leukemia &#40;CLL&#41;&#44; myelodysplastic syndrome &#40;MDS&#41;&#44; T-cell lymphoma&#47;leukemia &#40;TLL&#41;&#44; and rarely&#44; in hairy cell leukemia &#40;HCL&#41; and plasma cell leukemia &#40;PCL&#41;&#46;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;4&#44;6&#44;8</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">11</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">The frequency reported in the literature varies from 2&#46;1&#37; to 30&#37;&#44; depending on the type of primary leukemia&#44; but accurate and robust data are lacking&#46;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;4</span></a> In different studies&#44; there is also a problem in defining the terminology regarding the terms leukemia cutis&#44; myeloid sarcoma&#44; granulocytic sarcoma&#44; and chloroma&#44; which interferes with the epidemiological data&#46; Myeloid&#47;granulocytic sarcoma is described in the central nervous system&#44; gastrointestinal tract&#44; lymph nodes&#44; testes&#44; ovaries&#44; bones and peritoneum&#44; in addition to the skin&#46; Its occurrence is linked to leukemic diseases of the myeloid cell line&#44; mainly AML&#44; but it also occurs in CML&#44; MDS&#44; and other myeloproliferative disorders&#46;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6&#44;12</span></a> The word &#8220;chloroma&#8221;&#44; historically described in the 19<span class="elsevierStyleSup">th</span> century&#44; comes from the Greek word <span class="elsevierStyleItalic">chloros</span>&#46; which means green&#44; due to the greenish aspect of the tumor caused by myeloperoxidase oxidation&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">13</span></a> The terms granulocytic&#47;myeloid sarcoma emerged around 1965&#44; but they do not contemplate the actual origin of the tumor&#44; which occurs in hematopoietic tissue&#59;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> therefore&#44; the WHO in 2016&#44; defined myeloid sarcoma as a tumor mass of myeloid blasts with or without maturation&#44; which occurs at any anatomical site other than the bone marrow&#46; The term chloroma remains in use although not all cases have granules containing myeloperoxidase&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">13</span></a> This review follows the recommendations given by Vega et al&#46;&#44; where leukemia cutis is a broad term that encompasses the cutaneous infiltrations of any type of leukemia&#44; including myeloid sarcoma&#44; granulocytic sarcoma&#44; or chloroma&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">14</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">Considering the different types of leukemias&#44; a prevalence of LC of 10&#37; to 15&#37; is observed in AML&#44;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;3&#44;8&#44;9</span></a> of which the myelomonocytic &#40;AMML&#41; and monocytic &#40;MoAL&#41; subtypes are the most affected&#44; in up to half of the cases&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;5&#44;6</span></a> In CLL&#44; the most common presentation of systemic leukemias&#44; LC is reported in 4&#37; to 27&#37; of these cases&#44;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;15&#44;16</span></a> more frequently in the Richter&#8217;s syndrome&#44; which is the rare transformation of CLL into a large cell lymphoma&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">15</span></a> Regarding the other types of leukemia&#44; data show the involvement of 1&#37; to 3&#37; in ALL and 2&#37; in CML&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">The pathogenetic mechanism of skin invasion by leukemic cells is not well understood&#44; suggesting that chemokine receptors and adhesion molecules play a crucial role&#46; The role of cytogenetic alterations related to this type of tumor is also being studied&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;6&#44;11</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">Clinically&#44; the lesions are not pathognomonic&#44; as they are polymorphic&#44; single or&#44; mainly&#44; multiple &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">7&#44;10</span></a> The disease does not have a preferred location&#44; despite being more commonly described on the trunk&#44; extremities&#44; and face&#44;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6&#44;8</span></a> but it is rarely seen in the palmoplantar region&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> Some authors mention that the infiltration occurs preferentially in sites with previous skin inflammation or infection&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">8&#44;14&#44;16</span></a> Lesion morphology does not allows the diagnosis of the involved cell line&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;3&#44;6</span></a> They present as nodules&#44; plaques and papules of varied consistency&#44; are usually firm&#44; of various sizes&#44; and are brownish&#44; erythematous&#44; and&#47;or violaceous&#44; often purpuric in color &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41; due to the accompanying thrombocytopenia&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;4</span></a> The surface is usually smooth&#44; &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#44; but erosions&#44; ulcerations&#44; and the presence of desquamation are sometimes observed&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> Other clinical presentations of leukemia cutis are very rare&#44; such as maculopapular exanthema&#44; exfoliative erythroderma&#44; and single&#44; rarely multiple&#44; ulcers&#46;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;4&#44;7</span></a> Atypical presentations have been described in isolated cases&#44; such as psoriasiform lesions&#44; leonine facies&#44; figured macules&#44; papulovesicular lesions&#46;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;17</span></a> The aleukemic form is described as diffuse and papulonodular&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> More than 80&#37; of the skin lesions are asymptomatic&#44; few patients report pain or pruritus&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> The location and distribution also do not correlate with any specific cell type of leukemia cutis&#59;<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">10&#44;12</span></a> however&#44; some authors associate the generalized conditions with acute forms of leukemia&#44; while solitary&#44; clustered&#44; or dispersed lesions may be seen in chronic or acute forms&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> The dynamics of the appearance of infiltrations are also related to the type of leukemia&#44; with the ones with rapid onset&#44; in outbreaks&#44; being associated with acute forms&#44; while the ones with gradual onset are associated with chronic forms&#46; In CLL&#44; specific cutaneous lesions appear in the later stages of the disease&#44; approximately 40 months after the first systemic manifestations&#46;<a class="elsevierStyleCrossRefs" href="#bib0075"><span class="elsevierStyleSup">15&#44;16</span></a></p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0045" class="elsevierStylePara elsevierViewall">The oral mucosa can be affected and gingival hyperplasia is the most frequently observed clinical condition&#44; often hemorrhagic with evolution to necrosis&#46;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;4</span></a> This type of mucosal involvement is seen especially in AML and AMML&#46; Oral ulcers&#44; papules&#44; and nodules are rarely seen in CLL and other leukemias&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">Leukemia cutis is seen in 1&#47;3 of systemic leukemia cases in childhood&#44; mainly in the congenital forms&#46; <a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#44;18&#44;19</span></a> AML is the type of leukemia most often associated with LC in this age group&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">18</span></a> In congenital leukemia&#44; the lesions have a &#8220;blueberry muffin&#8221; appearance in 30&#37; of cases&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">14</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">When correlating the temporality of the cutaneous involvement onset in relation to the systemic one&#44; in 55&#37; to 77&#37; of the cases LC lesions appear in cases already diagnosed with leukemia&#44;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> and only in 23&#37; to 38&#37; of cases they appear concomitantly with systemic manifestations&#46;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;7&#44;8</span></a> In a recent study&#44; Yook et al&#46; &#40;2022&#41; reported that 71&#37; to 100&#37; of LC cases appear at or after the diagnosis of systemic leukemia&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">Skin biopsy is the reference examination for diagnosis&#44; which is based on histopathological evaluation&#44; considering the pattern of distribution&#44; cytological findings&#44; and immunohistochemical characteristics&#46;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;10&#44;12</span></a> Cytological characteristic vary with the type of underlying leukemia&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> The infiltrate is perivascular and&#47;or peri-adnexal&#44; nodular or diffuse&#44; occupying mainly the deep dermis and subcutaneous tissue&#44; with necrotic cells&#44; mitotic figures&#44; and nuclear pleomorphism&#46;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;14&#44;17</span></a> Immunohistochemical analysis helps to identify the cell line&#44; especially in cases of diagnostic doubt regarding cutaneous lymphoma&#46; Myeloid alterations are diagnosed by the absence of specific T and B-cell markers and by the expression of myelomonocytic markers such as CD68&#44; CD43&#44; CD33&#44; lysozyme&#44; myeloperoxidase&#44; CD117&#44; and CD15&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">16</span></a> LC in CLL is characterized by the co-expression of CD19&#44; CD5&#44; CD20&#44; CD79 and CD23&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">16</span></a> Immunohistochemical findings should always be correlated with bone marrow and peripheral blood findings&#44; in addition to molecular genetic studies&#46;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6&#44;10</span></a> In cases of no history of leukemia&#44; the diagnosis can be difficult&#44; as the cells may be poorly differentiated and diagnostic difficulty occurs&#44; confusing it with non-Hodgkin&#39;s lymphoma&#46;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6&#44;12</span></a> Imaging studies collaborate in cases of subcutaneous nodules&#44; contributing to establishing lesion location&#44; assessing the number of lesions&#44; and differential diagnoses&#46;<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">20</span></a></p><p id="par0065" class="elsevierStylePara elsevierViewall">There is no consensus on the treatment of leukemia cutis&#46; Systemic treatment is aimed at treating the underlying disease and there are few randomized trials that specifically assess the response&#46; The choice of protocol depends on the cell line involved&#44; immunohistochemical characteristics&#44; and time of onset in relation to systemic disease and cytogenetic alterations&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> The time of evolution is crucial in this choice and one should also consider whether or not the case is a recurrence&#46; Based on this knowledge&#44; traditional anti-leukemia chemotherapy&#44; consolidation with allogeneic bone marrow transplantation &#40;BMT&#41;&#44; or rescue with donor lymphocyte infusion &#40;DLI&#41; in post-allogeneic BMT are chosen&#46;<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#44;12</span></a> Radiotherapy that addresses the lesion locally can also be used&#44; especially in an isolated lesion&#44; in recurrence after BMT&#44; or in cases where symptoms caused by the tumor&#44; due to compression&#44; need to be quickly relieved&#46;<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#44;6</span></a></p><p id="par0070" class="elsevierStylePara elsevierViewall">Several studies associate the presence of leukemia cutis with an unfavorable prognosis when compared to the overall survival rate for systemic disease&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;7&#44;12</span></a> Considering the chronic disease&#44; the onset of LC demonstrates the presence of the blast phase&#44; which suggests progression to the acute form&#46;<a class="elsevierStyleCrossRefs" href="#bib0070"><span class="elsevierStyleSup">14&#44;21</span></a> Possible cytogenetic abnormalities detected through karyotype and fluorescence <span class="elsevierStyleItalic">in situ</span> hybridization &#40;FISH&#41; studies demonstrate aggressive behavior&#46;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">17</span></a> Existing data indicate that survival after one year is very low&#44; based on studies with small sample sizes&#46;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6&#44;17</span></a> In the study by Chang et al&#46;&#44; 74&#46;3&#37; of LC cases died within one year and the median survival was 7&#46;2 months&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> Yook et al&#46; &#40;2022&#41; demonstrated that 84&#37; of the patients died after the LC diagnosis&#44; of which 93&#37; of them died within 10 months&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> LC-associated survival in AML and AMML cases is as low as four months&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> A 2019 cohort study shows that patients with AML and leukemia cutis are 2&#46;06 times more likely to die than patients without skin infiltration&#46;<a class="elsevierStyleCrossRef" href="#bib0105"><span class="elsevierStyleSup">21</span></a> Data on CLL show that the prognosis is associated with the histological characteristics&#44; being poor &#8210; 49&#37; survival at 2 years &#8210; when there are more than 5&#37; of large B lymphocytes in the cutaneous infiltrate and favorable &#8211; 97&#37; survival at 2 years &#8210; when there are more than 95&#37; small B lymphocytes&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">16</span></a> Recent studies demonstrate that in the absence of systemic disease progression&#44; such as for Richter&#39;s syndrome&#44; leukemia cutis in CLL does not lead to worsening of the prognosis&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">15</span></a> However&#44; the literature is still scarce and conflicting when assessing leukemia cutis and the prognosis of the underlying disease&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a></p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Cutaneous plasmacytoma</span><p id="par0075" class="elsevierStylePara elsevierViewall">Plasma cell dyscrasias are characterized by the clonal neoplastic expansion of cells that secrete monoclonal immunoglobulins&#46; The clinical spectrum is diverse and groups entities of different degrees of severity&#44; from asymptomatic monoclonal gammopathy of uncertain significance &#40;MGUS&#41; to malignancies of greater clinical severity&#44; such as multiple myeloma &#40;MM&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0110"><span class="elsevierStyleSup">22</span></a></p><p id="par0080" class="elsevierStylePara elsevierViewall">Cutaneous plasmacytoma is a rare neoplasm of plasma cells that infiltrates the skin&#44; either by direct involvement&#44; by contiguity of a close focus&#44; or at a distance&#44; via a hematogenous or lymphatic route&#46;<a class="elsevierStyleCrossRefs" href="#bib0110"><span class="elsevierStyleSup">22&#44;23</span></a> The most often described cutaneous plasmacytomas arise in the context of MM&#44; usually as a late complication&#46;<a class="elsevierStyleCrossRef" href="#bib0120"><span class="elsevierStyleSup">24</span></a> There are few reports in the literature&#44; occurring in less than 4&#37; of cases&#44; although some authors believe that underdiagnosis occurs since in autopsy data of patients with MM the number of extramedullary cutaneous involvement is much higher&#46;<a class="elsevierStyleCrossRefs" href="#bib0120"><span class="elsevierStyleSup">24&#8211;26</span></a> There is a much rarer form&#44; primary cutaneous plasmacytoma&#44; which occurs without evidence of another medullary or extramedullary plasma cell disease&#44; currently classified in the group of marginal zone lymphomas&#46; Cutaneous plasmacytomas are associated with all immunoglobulin classes&#44; with the exception of IgE&#44; and those related to IgG are the most frequently observed&#46;<a class="elsevierStyleCrossRef" href="#bib0115"><span class="elsevierStyleSup">23</span></a></p><p id="par0085" class="elsevierStylePara elsevierViewall">The most representative clinical form is isolated&#44; smooth&#44; rounded erythematous-violaceous nodules &#40;<a class="elsevierStyleCrossRef" href="#fig0020">Fig&#46; 4</a>&#41;&#44; but there have been descriptions of flesh-colored nodules in rare cases&#46;<a class="elsevierStyleCrossRef" href="#bib0130"><span class="elsevierStyleSup">26</span></a> There is no difference in the clinical picture according to the immunoglobulin involved&#46;</p><elsevierMultimedia ident="fig0020"></elsevierMultimedia><p id="par0090" class="elsevierStylePara elsevierViewall">Studies demonstrate that the tumor microenvironment is the main regulator of the metastatic process in the extramedullary involvement of plasma cell neoplasms&#44; but the exact mechanism is not yet understood&#46;<a class="elsevierStyleCrossRef" href="#bib0130"><span class="elsevierStyleSup">26</span></a></p><p id="par0095" class="elsevierStylePara elsevierViewall">A biopsy with histopathological and immunohistochemical analyses confirms the diagnosis&#46; A nodular plasma cell infiltrate is the main identified pattern&#44; followed by the interstitial one&#46; The presence of immunoreactivity for CD138 is constant&#44; in addition to the frequent absence of expression of CD45 and CD20&#46;<a class="elsevierStyleCrossRefs" href="#bib0120"><span class="elsevierStyleSup">24&#44;26</span></a></p><p id="par0100" class="elsevierStylePara elsevierViewall">Prognosis is poor and the mean survival time is 8&#46;5 months&#46;<a class="elsevierStyleCrossRefs" href="#bib0120"><span class="elsevierStyleSup">24&#44;25</span></a> Deletion of the RB1 gene has been reported to be associated with worse prognosis&#46;<a class="elsevierStyleCrossRef" href="#bib0120"><span class="elsevierStyleSup">24</span></a></p><p id="par0105" class="elsevierStylePara elsevierViewall">Treatment of plasmacytomas with systemic involvement is that of the underlying disease&#44; with or without associated radiotherapy&#46; Primary cutaneous plasmacytomas are treated with radiotherapy alone&#44; or by surgery followed by localized radiotherapy and&#47;or chemotherapy&#46;<a class="elsevierStyleCrossRef" href="#bib0125"><span class="elsevierStyleSup">25</span></a></p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Secondary cutaneous lymphomas</span><p id="par0110" class="elsevierStylePara elsevierViewall">Cutaneous lymphomas can be subdivided into two broad groups&#58; primary&#44; in which there is no evidence of extracutaneous disease at the time of diagnosis&#44; and those that are secondary to systemic lymphoma&#46;<a class="elsevierStyleCrossRef" href="#bib0135"><span class="elsevierStyleSup">27</span></a> Primary cutaneous lymphomas &#40;PCL&#41; represent a heterogeneous group of entities and will not be addressed in this review&#46;</p><p id="par0115" class="elsevierStylePara elsevierViewall">Secondary cutaneous lymphomas &#40;SCL&#41; account for 20&#37; to 50&#37; of cutaneous lymphomas&#46;<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">28</span></a> They can be classified&#44; according to the cell line that originated them&#44; as T&#47;NK lymphoma or B lymphoma&#46;<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">28</span></a> Among the reported cases of SCL in the literature&#44; the relative frequency of the mature T&#47;NK cell line ranged from 48&#37; to 72&#37; in different studies&#44; whereas the mature B line ranged from 21&#37; to 45&#37;&#44; immature hematological neoplasms corresponded to 4&#37; to 8&#37; of cases and Hodgkin&#39;s lymphoma accounted for 0&#37; to 4&#37; of cases&#46;<a class="elsevierStyleCrossRefs" href="#bib0140"><span class="elsevierStyleSup">28&#8211;32</span></a></p><p id="par0120" class="elsevierStylePara elsevierViewall">The clinical manifestations of SCL are polymorphic&#46; Nodules are often present &#40;<a class="elsevierStyleCrossRef" href="#fig0025">Fig&#46; 5</a>&#41; in up to 60&#37; of cases&#44; but macules&#44; patches&#44; and plaques can also occur&#46; Ulceration occurs in up to 9&#37; of cases&#46; Lesion morphology did not correlate with survival in one case series&#46;<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">28</span></a></p><elsevierMultimedia ident="fig0025"></elsevierMultimedia><p id="par0125" class="elsevierStylePara elsevierViewall">Patients with T&#47;NK line SCL more often manifest multiple or disseminated lesions and the presence of these lesions is a poor prognostic factor&#46;<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">28</span></a> Peripheral T-cell lymphomas may present clinically as nodules or tumors&#44; but generalized maculopapular or urticarial eruptions have been described&#44; with lesion morphology varying in the same patient over time&#46;<a class="elsevierStyleCrossRef" href="#bib0165"><span class="elsevierStyleSup">33</span></a></p><p id="par0130" class="elsevierStylePara elsevierViewall">Regarding CD30&#43; anaplastic lymphomas&#44; there are also significant differences between the primary cutaneous form and the secondary form&#46; The secondary CD30&#43; anaplastic cutaneous lymphoma &#40;<a class="elsevierStyleCrossRef" href="#fig0030">Fig&#46; 6</a>&#41; is more often characterized by papules and nodules&#44; has a higher frequency of B symptoms&#44; and has a worse prognosis&#44; with higher mortality and shorter five-year survival&#46;<a class="elsevierStyleCrossRef" href="#bib0170"><span class="elsevierStyleSup">34</span></a></p><elsevierMultimedia ident="fig0030"></elsevierMultimedia><p id="par0135" class="elsevierStylePara elsevierViewall">Hodgkin&#39;s lymphoma is associated with specific cutaneous manifestations in less than 1&#37; of cases&#44; usually in advanced refractory disease&#46;<a class="elsevierStyleCrossRef" href="#bib0175"><span class="elsevierStyleSup">35</span></a> The mode of spread is by direct extension of neoplastic cells to the skin&#46;<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">36</span></a> Skin involvement by direct extension has also been described in high-grade nodal B lymphomas&#46;<a class="elsevierStyleCrossRef" href="#bib0185"><span class="elsevierStyleSup">37</span></a></p><p id="par0140" class="elsevierStylePara elsevierViewall">The diagnosis of SCL depends on the diagnosis of the associated nodal lymphoma&#46; The diagnosis of lymphomas is a complex one and includes clinical&#44; morphological&#44; histopathological&#44; immunohistochemical&#44; and molecular factors&#46;<a class="elsevierStyleCrossRef" href="#bib0190"><span class="elsevierStyleSup">38</span></a> The immunophenotype of CD20 and CD79a expression identifies B-cell line lymphomas&#44; while the CD3 marker&#44; as well as CD2&#44; CD7&#44; and LAT markers&#44; identify the T-cell line&#46; Other markers used for the diagnosis and classification of lymphomas are the panlymphocytic marker CD45&#44; the NK cell marker CD56&#44; and other cytotoxic markers for T and NK cells&#46; Very often&#44; only clinical&#44; histopathological&#44; and immunohistochemical factors are not enough to establish the diagnosis of lymphoma&#46; In these cases&#44; molecular methods are also used to investigate clonality and identify the cell line involved&#46;<a class="elsevierStyleCrossRef" href="#bib0190"><span class="elsevierStyleSup">38</span></a> To differentiate between PCL and SCL&#44; it is necessary to perform the patient&#8217;s staging through imaging tests&#44; bone marrow biopsy&#44; peripheral blood flow cytometry&#44; or other methods&#44; aiming to assess the presence of nodal or other organ involvement at the time of diagnosis&#44; which characterizes the SCL&#46;</p><p id="par0145" class="elsevierStylePara elsevierViewall">When skin involvement occurs within the first six months of diagnosis&#44; the prognosis is worse than in cases in which these lesions occur six months after the diagnosis&#46;<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">28</span></a> When compared to PCL&#44; SCL have worse five-year survival&#46; The five-year survival for SCL is 31&#37;&#44; while for PCL it ranges from 87&#37; to 92&#46;5&#37;&#46;<a class="elsevierStyleCrossRef" href="#bib0195"><span class="elsevierStyleSup">39</span></a></p><p id="par0150" class="elsevierStylePara elsevierViewall">Treatment of SCL comprises the treatment of the nodal lymphoma that caused it&#46; Radiotherapy alone is chosen for the localized forms or combined with chemotherapy for aggressive disease&#46; For B-lymphomas&#44; the anti-CD20 antibody rituximab is frequently used&#44; together or not with multidrug chemotherapy&#46; Other treatments used in refractory lymphomas include brentuximab vedotin&#44; ibrutinib&#44; acalabrutinib and idelalisib&#46; Immunotherapy with checkpoint inhibitors has also been associated in recent years in the therapeutic arsenal used to treat lymphomas&#46;<a class="elsevierStyleCrossRef" href="#bib0200"><span class="elsevierStyleSup">40</span></a> Bone marrow transplantation is an alternative for refractory cases&#46; CAR-T &#40;chimeric antigen receptor T&#41; cells have also shown promising results in refractory hematologic malignancies&#46;<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">41</span></a></p></span></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Conclusion</span><p id="par0155" class="elsevierStylePara elsevierViewall">In part I of this review&#44; the authors demonstrate to dermatologists&#44; hematologists&#44; and clinicians the importance of a complete dermatological examination and familiarity with the skin alterations&#44; which may represent a neoplastic infiltration of an already known condition or even a lesion that precedes the diagnosis of systemic disease&#46; Etiological elucidation always needs to be confirmed by a skin biopsy with anatomopathological and immunohistochemical examination&#46; The identification of this type of extramedullary lesion helps in the decision-making related to treatment&#44; which&#44; if performed early&#44; may change prognosis&#46;</p><p id="par0160" class="elsevierStylePara elsevierViewall">More epidemiological work is required in this area of &#8203;&#8203;knowledge&#44; aiming to obtain robust and reliable statistical data&#46; It is important to highlights the need for multidisciplinary team working for this complex type of patient&#44; in which the dermatologist is the specialist responsible for the evaluation and diagnosis of skin alterations&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Financial support</span><p id="par0165" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Authors&#39; contributions</span><p id="par0170" class="elsevierStylePara elsevierViewall">Patricia Karla de Souza&#58; Design of the study&#59; drafting of the manuscript and critical review of important intellectual content&#59; design of the study together with the co-authors&#59; critical review of the literature&#59; approval of the final version of the manuscript&#46;</p><p id="par0175" class="elsevierStylePara elsevierViewall">Rafael Oliveira Amorim&#58; Drafting of the manuscript and critical review of important intellectual content&#59; design of the study together with the co-authors&#59; critical review of the literature&#59; approval of the final version of the manuscript&#46;</p><p id="par0180" class="elsevierStylePara elsevierViewall">Let&#237;cia Siqueira Sousa&#58; Drafting of the manuscript and critical review of important intellectual content&#59; design of the study together with the co-authors&#59; critical review of the literature&#59; approval of the final version of the manuscript&#46;</p><p id="par0185" class="elsevierStylePara elsevierViewall">Mariana Dias Batista&#58; Drafting of the manuscript and critical review of important intellectual content&#59; design of the study together with the co-authors&#59; critical review of the literature&#59; approval of the final version of the manuscript&#46;</p></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0055">Conflicts of interest</span><p id="par0190" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span></span>"
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          "titulo" => "Abstract"
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          "titulo" => "Introduction"
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          "identificador" => "sec0010"
          "titulo" => "Specific skin lesions secondary to systemic hematologic malignancy infiltration"
          "secciones" => array:3 [
            0 => array:2 [
              "identificador" => "sec0015"
              "titulo" => "Leukemia cutis"
            ]
            1 => array:2 [
              "identificador" => "sec0020"
              "titulo" => "Cutaneous plasmacytoma"
            ]
            2 => array:2 [
              "identificador" => "sec0025"
              "titulo" => "Secondary cutaneous lymphomas"
            ]
          ]
        ]
        4 => array:2 [
          "identificador" => "sec0030"
          "titulo" => "Conclusion"
        ]
        5 => array:2 [
          "identificador" => "sec0035"
          "titulo" => "Financial support"
        ]
        6 => array:2 [
          "identificador" => "sec0040"
          "titulo" => "Authors&#39; contributions"
        ]
        7 => array:2 [
          "identificador" => "sec0045"
          "titulo" => "Conflicts of interest"
        ]
        8 => array:1 [
          "titulo" => "References"
        ]
      ]
    ]
    "pdfFichero" => "main.pdf"
    "tienePdf" => true
    "fechaRecibido" => "2021-12-12"
    "fechaAceptado" => "2022-06-03"
    "PalabrasClave" => array:1 [
      "en" => array:1 [
        0 => array:4 [
          "clase" => "keyword"
          "titulo" => "Keywords"
          "identificador" => "xpalclavsec1630590"
          "palabras" => array:4 [
            0 => "Leukemia&#44; myeloid"
            1 => "Lymphoma"
            2 => "Plasmacytoma"
            3 => "Skin neoplasms"
          ]
        ]
      ]
    ]
    "tieneResumen" => true
    "resumen" => array:1 [
      "en" => array:2 [
        "titulo" => "Abstract"
        "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Cutaneous manifestations occur during the course of hematologic malignancies and precede&#44; follow&#44; or are late events in relation to the diagnosis&#46; They result from paraneoplastic phenomena&#44; tumor infiltrations&#44; and immunosuppression resulting from the hematologic neoplasia itself or its treatment&#46; The dermatologist must be aware of these conditions&#44; which can help both in the diagnosis of the underlying disease and in the reduction of patient morbidity&#46; This review &#40;part I&#41; addresses skin lesions associated with direct infiltration by systemic hematologic malignancies&#46;</p></span>"
      ]
    ]
    "NotaPie" => array:1 [
      0 => array:2 [
        "etiqueta" => "&#9734;"
        "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Study conducted at the Hospital Israelita Albert Einstein&#44; S&#227;o Paulo&#44; SP&#44; Brazil and at the Department of Dermatology&#44; Universidade Federal de S&#227;o Paulo&#44; S&#227;o Paulo&#44; SP&#44; Brazil&#46;</p>"
      ]
    ]
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        "etiqueta" => "Figure 1"
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        "figura" => array:1 [
          0 => array:4 [
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          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Leukemia cutis in a patient with AML&#46; &#40;A&#41;&#44; Multiple erythematous&#44; infiltrated papules and nodules with a smooth surface affecting the trunk and upper limb&#46; &#40;B&#41; Lesions at higher magnification&#46;</p>"
        ]
      ]
      1 => array:8 [
        "identificador" => "fig0010"
        "etiqueta" => "Figure 2"
        "tipo" => "MULTIMEDIAFIGURA"
        "mostrarFloat" => true
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        "figura" => array:1 [
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          "en" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Leukemia cutis in a patient with AML &#8210; confluent purpuric papules and some isolated ones with a rough surface on the lateral aspect of the left arm&#46;</p>"
        ]
      ]
      2 => array:8 [
        "identificador" => "fig0015"
        "etiqueta" => "Figure 3"
        "tipo" => "MULTIMEDIAFIGURA"
        "mostrarFloat" => true
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          "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Leukemia cutis in a patient with AML&#46; &#40;A&#41; Post-allogeneic BMT recurrence &#8211; two isolated erythematous&#44; smooth&#44; hardened papules on both thighs&#46; &#40;B&#41;&#44; Detail of the lesion at higher magnification&#46;</p>"
        ]
      ]
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        "mostrarFloat" => true
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        "descripcion" => array:1 [
          "en" => "<p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Cutaneous plasmacytoma&#46; Erythematous-violaceous nodules&#44; poorly defined and infiltrated in the periumbilical region&#46;</p>"
        ]
      ]
      4 => array:8 [
        "identificador" => "fig0025"
        "etiqueta" => "Figure 5"
        "tipo" => "MULTIMEDIAFIGURA"
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        "descripcion" => array:1 [
          "en" => "<p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Secondary cutaneous follicular lymphoma&#46; &#40;A&#41; Brownish-erythematous&#44; infiltrated subcutaneous tumor&#44; with telangiectasias in the epigastric region&#46; &#40;B&#41; Lesion at higher magnification&#46;</p>"
        ]
      ]
      5 => array:8 [
        "identificador" => "fig0030"
        "etiqueta" => "Figure 6"
        "tipo" => "MULTIMEDIAFIGURA"
        "mostrarFloat" => true
        "mostrarDisplay" => false
        "figura" => array:1 [
          0 => array:4 [
            "imagen" => "gr6.jpeg"
            "Alto" => 2290
            "Ancho" => 1508
            "Tamanyo" => 247039
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          0 => array:3 [
            "identificador" => "at0090"
            "detalle" => "Figure "
            "rol" => "short"
          ]
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        "descripcion" => array:1 [
          "en" => "<p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Secondary cutaneous CD30&#43; anaplastic lymphoma &#8211; erythematous&#44; infiltrated&#44; raised&#44; reddish plaque in the central portion on the posterior right axillary line&#46;</p>"
        ]
      ]
      6 => array:8 [
        "identificador" => "tbl0005"
        "etiqueta" => "Table 1"
        "tipo" => "MULTIMEDIATABLA"
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        "detalles" => array:1 [
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        "tabla" => array:1 [
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              "tabla" => array:1 [
                0 => """
                  <table border="0" frame="\n
                  \t\t\t\t\tvoid\n
                  \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Dermatological diagnosis&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Most frequently found hematologic alteration&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Typical dermatological manifestation&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Management&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead rowgroup " rowspan="6" align="left" valign="middle">Leukemia cutis</td><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">AML&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " rowspan="2" align="left" valign="middle">Firm&#44; smooth&#44; brownish&#44; erythematous&#44; and&#47;or violaceous nodules&#44; plaques&#44; and papules</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " rowspan="2" align="left" valign="middle">Anti-leukemia pharmacological treatment</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead rowgroup " rowspan="5" align="left" valign="middle">Others&#58; CLL&#44; AMML&#44; MDS&#44; ALL&#44; T-cell lymphoma&#47;leukemia</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Erosions&#44; ulcerations&#44; occasional desquamation&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Allogeneic BMT&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Trunk&#44; extremities&#44; face&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " rowspan="2" align="left" valign="middle">Rescue with DLI &#40;donor lymphocyte infusion&#41; in post-allogeneic BMT recurrence</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead rowgroup " rowspan="2" align="left" valign="middle">Mucosa&#58; gingival hyperplasia</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Radiotherapy&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead rowgroup " rowspan="2" align="left" valign="middle">Cutaneous plasmacytoma</td><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " rowspan="2" align="left" valign="middle">MM</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " rowspan="2" align="left" valign="middle">Erythematous-violaceous&#44; isolated&#44; smooth&#44; rounded nodules</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Treatment of the underlying disease &#43;&#47;- Radiotherapy&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Cutaneous primary&#58; Radiotherapy&#59; Surgery followed by radiation or chemotherapy&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead rowgroup " rowspan="4" align="left" valign="middle">Secondary cutaneous lymphomas</td><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">T&#47;NK line&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Nodules &#40;60&#37; of cases&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " rowspan="4" align="left" valign="middle">Treatment of underlying lymphoma</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead rowgroup " rowspan="3" align="left" valign="middle">Other&#58; Mature B-line&#44; immature hematologic malignancies&#44; Hodgkin&#39;s lymphoma</td><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Macules&#44; patches and plaques&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Ulceration &#40;9&#37; of cases&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">T&#47;NK line&#58; multiple&#47;widespread lesions&#59; poor prognosis&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr></tbody></table>
                  """
              ]
            ]
          ]
        ]
        "descripcion" => array:1 [
          "en" => "<p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Specific cutaneous manifestations of hematologic neoplasms&#58; associations and management&#46;</p>"
        ]
      ]
      7 => array:8 [
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        "etiqueta" => "Table 2"
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                0 => """
                  <table border="0" frame="\n
                  \t\t\t\t\tvoid\n
                  \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Dermatological Diagnosis&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Epidemiological data&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead rowgroup " rowspan="4" align="left" valign="middle">Leukemia cutis &#40;prevalence&#41;</td><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">AML&#8211; 10&#37;&#8210;15&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">CLL &#8211; 4&#37;&#8210;27&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">ALL &#8211; 1&#37;&#8210;3&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">CLM &#8211; 2&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " colspan="2" align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Cutaneous plasmacytoma &#40;prevalence&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">MM &#8211; 4&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead rowgroup " rowspan="4" align="left" valign="middle">Secondary cutaneous lymphomas &#40;relative frequency&#41;</td><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">T&#47;NK line &#8211; 48&#37;&#8210;72&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Mature B line &#8211; 21&#37;&#8210;25&#37;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t\ttable-entry\n
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Journal Information
Vol. 98. Issue 1.
Pages 5-12 (1 January 2023)
Visits
7640
Vol. 98. Issue 1.
Pages 5-12 (1 January 2023)
Continuing Medical Education
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Dermatological manifestations of hematologic neoplasms. Part I: secondary specific skin lesions
Visits
7640
Patricia Karla de Souzaa, Rafael Oliveira Amorimb,
Corresponding author
rafaelamorim78@gmail.com

Corresponding author.
, Letícia Siqueira Sousaa, Mariana Dias Batistab
a Hospital Israelita Albert Einstein, São Paulo, SP, Brazil
b Department of Dermatology, Universidade Federal de São Paulo, São Paulo, SP, Brazil
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Abstract

Cutaneous manifestations occur during the course of hematologic malignancies and precede, follow, or are late events in relation to the diagnosis. They result from paraneoplastic phenomena, tumor infiltrations, and immunosuppression resulting from the hematologic neoplasia itself or its treatment. The dermatologist must be aware of these conditions, which can help both in the diagnosis of the underlying disease and in the reduction of patient morbidity. This review (part I) addresses skin lesions associated with direct infiltration by systemic hematologic malignancies.

Keywords:
Leukemia, myeloid
Lymphoma
Plasmacytoma
Skin neoplasms
Full Text
Introduction

Hematologic malignancies constitute a group of neoplasms with extremely heterogeneous clinical and behavioral characteristics that lead to aggressive or indolent, acute or chronic conditions, with different prognoses and involvement of different organs.1 The skin may be involved in a specific way, through infiltration by malignant cells, or non-specific, as in paraneoplastic dermatoses, in alterations common to hematological disorders, such as pallor and ecchymosis, among others, and as those related to treatment and opportunistic infections.1,2 Cutaneous involvement substantially impacts the quality of life of the hematologic patient, in addition to compromising the prognosis in different cases.1

Specific skin lesions secondary to systemic hematologic malignancy infiltration (Part 1) and the most common paraneoplastic skin diseases associated with hematologic systemic neoplasms (Part 2) will be discussed. Primary cutaneous lymphomas will not be addressed. Table 1 briefly describes the reviewed conditions and their treatment and Table 2 the epidemiological data of these conditions, according to the literature.

Table 1.

Specific cutaneous manifestations of hematologic neoplasms: associations and management.

Dermatological diagnosis  Most frequently found hematologic alteration  Typical dermatological manifestation  Management 
Leukemia cutisAML  Firm, smooth, brownish, erythematous, and/or violaceous nodules, plaques, and papulesAnti-leukemia pharmacological treatment
Others: CLL, AMML, MDS, ALL, T-cell lymphoma/leukemia
Erosions, ulcerations, occasional desquamation  Allogeneic BMT 
Trunk, extremities, face  Rescue with DLI (donor lymphocyte infusion) in post-allogeneic BMT recurrence
Mucosa: gingival hyperplasia
Radiotherapy 
Cutaneous plasmacytomaMMErythematous-violaceous, isolated, smooth, rounded nodulesTreatment of the underlying disease +/- Radiotherapy 
Cutaneous primary: Radiotherapy; Surgery followed by radiation or chemotherapy 
Secondary cutaneous lymphomasT/NK line  Nodules (60% of cases)  Treatment of underlying lymphoma
Other: Mature B-line, immature hematologic malignancies, Hodgkin's lymphomaMacules, patches and plaques 
Ulceration (9% of cases) 
T/NK line: multiple/widespread lesions; poor prognosis 
Table 2.

Epidemiological data of the specific cutaneous manifestations of hematologic neoplasms.

Dermatological Diagnosis  Epidemiological data 
Leukemia cutis (prevalence)AML– 10%‒15% 
CLL – 4%‒27% 
ALL – 1%‒3% 
CLM – 2% 
Cutaneous plasmacytoma (prevalence)  MM – 4% 
Secondary cutaneous lymphomas (relative frequency)T/NK line – 48%‒72% 
Mature B line – 21%‒25% 
Immature hematologic neoplasms – 4%‒8% 
Hodgkin’s lymphoma – 0%‒4% 
Specific skin lesions secondary to systemic hematologic malignancy infiltrationLeukemia cutis

Leukemias are neoplastic proliferations of leukocytes and their precursors in the bone marrow and peripheral blood.3,4 They are myeloid or lymphoid in origin and, according to cell maturation, acute or chronic.5,6 Leukemia cutis (LC) is the extramedullary cutaneous manifestation caused by the infiltration of leukemic cells into the epidermis, dermis, or subcutaneous tissue.3,7 It appears before, during, or after the manifestation of the systemic disease as an extramedullary occurrence of the initial disease, as the first manifestation of the hematologic disease, or, rarely, as the primary disease. 7,8 The rare cases that occur before bone marrow or peripheral blood involvement, whose systemic involvement may take months to years to appear, are called aleukemic leukemias.9,10

Leukemia cutis most frequently affects individuals with acute myeloid leukemia (AML); however, it is also seen in chronic myeloid leukemia (CML), acute lymphocytic leukemia (ALL), chronic lymphocytic leukemia (CLL), myelodysplastic syndrome (MDS), T-cell lymphoma/leukemia (TLL), and rarely, in hairy cell leukemia (HCL) and plasma cell leukemia (PCL).3,4,6,8,11

The frequency reported in the literature varies from 2.1% to 30%, depending on the type of primary leukemia, but accurate and robust data are lacking.3,4 In different studies, there is also a problem in defining the terminology regarding the terms leukemia cutis, myeloid sarcoma, granulocytic sarcoma, and chloroma, which interferes with the epidemiological data. Myeloid/granulocytic sarcoma is described in the central nervous system, gastrointestinal tract, lymph nodes, testes, ovaries, bones and peritoneum, in addition to the skin. Its occurrence is linked to leukemic diseases of the myeloid cell line, mainly AML, but it also occurs in CML, MDS, and other myeloproliferative disorders.6,12 The word “chloroma”, historically described in the 19th century, comes from the Greek word chloros. which means green, due to the greenish aspect of the tumor caused by myeloperoxidase oxidation.13 The terms granulocytic/myeloid sarcoma emerged around 1965, but they do not contemplate the actual origin of the tumor, which occurs in hematopoietic tissue;3 therefore, the WHO in 2016, defined myeloid sarcoma as a tumor mass of myeloid blasts with or without maturation, which occurs at any anatomical site other than the bone marrow. The term chloroma remains in use although not all cases have granules containing myeloperoxidase.13 This review follows the recommendations given by Vega et al., where leukemia cutis is a broad term that encompasses the cutaneous infiltrations of any type of leukemia, including myeloid sarcoma, granulocytic sarcoma, or chloroma.14

Considering the different types of leukemias, a prevalence of LC of 10% to 15% is observed in AML,2,3,8,9 of which the myelomonocytic (AMML) and monocytic (MoAL) subtypes are the most affected, in up to half of the cases.2,5,6 In CLL, the most common presentation of systemic leukemias, LC is reported in 4% to 27% of these cases,3,15,16 more frequently in the Richter’s syndrome, which is the rare transformation of CLL into a large cell lymphoma.15 Regarding the other types of leukemia, data show the involvement of 1% to 3% in ALL and 2% in CML.9

The pathogenetic mechanism of skin invasion by leukemic cells is not well understood, suggesting that chemokine receptors and adhesion molecules play a crucial role. The role of cytogenetic alterations related to this type of tumor is also being studied.2,6,11

Clinically, the lesions are not pathognomonic, as they are polymorphic, single or, mainly, multiple (Fig. 1).7,10 The disease does not have a preferred location, despite being more commonly described on the trunk, extremities, and face,6,8 but it is rarely seen in the palmoplantar region.3 Some authors mention that the infiltration occurs preferentially in sites with previous skin inflammation or infection.8,14,16 Lesion morphology does not allows the diagnosis of the involved cell line.2,3,6 They present as nodules, plaques and papules of varied consistency, are usually firm, of various sizes, and are brownish, erythematous, and/or violaceous, often purpuric in color (Fig. 2) due to the accompanying thrombocytopenia.2,4 The surface is usually smooth, (Fig. 3), but erosions, ulcerations, and the presence of desquamation are sometimes observed.3 Other clinical presentations of leukemia cutis are very rare, such as maculopapular exanthema, exfoliative erythroderma, and single, rarely multiple, ulcers.3,4,7 Atypical presentations have been described in isolated cases, such as psoriasiform lesions, leonine facies, figured macules, papulovesicular lesions.3,17 The aleukemic form is described as diffuse and papulonodular.6 More than 80% of the skin lesions are asymptomatic, few patients report pain or pruritus.4 The location and distribution also do not correlate with any specific cell type of leukemia cutis;10,12 however, some authors associate the generalized conditions with acute forms of leukemia, while solitary, clustered, or dispersed lesions may be seen in chronic or acute forms.3 The dynamics of the appearance of infiltrations are also related to the type of leukemia, with the ones with rapid onset, in outbreaks, being associated with acute forms, while the ones with gradual onset are associated with chronic forms. In CLL, specific cutaneous lesions appear in the later stages of the disease, approximately 40 months after the first systemic manifestations.15,16

Figure 1.

Leukemia cutis in a patient with AML. (A), Multiple erythematous, infiltrated papules and nodules with a smooth surface affecting the trunk and upper limb. (B) Lesions at higher magnification.

(0.29MB).
Figure 2.

Leukemia cutis in a patient with AML ‒ confluent purpuric papules and some isolated ones with a rough surface on the lateral aspect of the left arm.

(0.11MB).
Figure 3.

Leukemia cutis in a patient with AML. (A) Post-allogeneic BMT recurrence – two isolated erythematous, smooth, hardened papules on both thighs. (B), Detail of the lesion at higher magnification.

(0.24MB).

The oral mucosa can be affected and gingival hyperplasia is the most frequently observed clinical condition, often hemorrhagic with evolution to necrosis.3,4 This type of mucosal involvement is seen especially in AML and AMML. Oral ulcers, papules, and nodules are rarely seen in CLL and other leukemias.3

Leukemia cutis is seen in 1/3 of systemic leukemia cases in childhood, mainly in the congenital forms. 4,18,19 AML is the type of leukemia most often associated with LC in this age group.18 In congenital leukemia, the lesions have a “blueberry muffin” appearance in 30% of cases.14

When correlating the temporality of the cutaneous involvement onset in relation to the systemic one, in 55% to 77% of the cases LC lesions appear in cases already diagnosed with leukemia,4 and only in 23% to 38% of cases they appear concomitantly with systemic manifestations.3,7,8 In a recent study, Yook et al. (2022) reported that 71% to 100% of LC cases appear at or after the diagnosis of systemic leukemia.9

Skin biopsy is the reference examination for diagnosis, which is based on histopathological evaluation, considering the pattern of distribution, cytological findings, and immunohistochemical characteristics.3,10,12 Cytological characteristic vary with the type of underlying leukemia.10 The infiltrate is perivascular and/or peri-adnexal, nodular or diffuse, occupying mainly the deep dermis and subcutaneous tissue, with necrotic cells, mitotic figures, and nuclear pleomorphism.3,14,17 Immunohistochemical analysis helps to identify the cell line, especially in cases of diagnostic doubt regarding cutaneous lymphoma. Myeloid alterations are diagnosed by the absence of specific T and B-cell markers and by the expression of myelomonocytic markers such as CD68, CD43, CD33, lysozyme, myeloperoxidase, CD117, and CD15.16 LC in CLL is characterized by the co-expression of CD19, CD5, CD20, CD79 and CD23.16 Immunohistochemical findings should always be correlated with bone marrow and peripheral blood findings, in addition to molecular genetic studies.6,10 In cases of no history of leukemia, the diagnosis can be difficult, as the cells may be poorly differentiated and diagnostic difficulty occurs, confusing it with non-Hodgkin's lymphoma.6,12 Imaging studies collaborate in cases of subcutaneous nodules, contributing to establishing lesion location, assessing the number of lesions, and differential diagnoses.20

There is no consensus on the treatment of leukemia cutis. Systemic treatment is aimed at treating the underlying disease and there are few randomized trials that specifically assess the response. The choice of protocol depends on the cell line involved, immunohistochemical characteristics, and time of onset in relation to systemic disease and cytogenetic alterations.10 The time of evolution is crucial in this choice and one should also consider whether or not the case is a recurrence. Based on this knowledge, traditional anti-leukemia chemotherapy, consolidation with allogeneic bone marrow transplantation (BMT), or rescue with donor lymphocyte infusion (DLI) in post-allogeneic BMT are chosen.4,12 Radiotherapy that addresses the lesion locally can also be used, especially in an isolated lesion, in recurrence after BMT, or in cases where symptoms caused by the tumor, due to compression, need to be quickly relieved.4,6

Several studies associate the presence of leukemia cutis with an unfavorable prognosis when compared to the overall survival rate for systemic disease.2,7,12 Considering the chronic disease, the onset of LC demonstrates the presence of the blast phase, which suggests progression to the acute form.14,21 Possible cytogenetic abnormalities detected through karyotype and fluorescence in situ hybridization (FISH) studies demonstrate aggressive behavior.17 Existing data indicate that survival after one year is very low, based on studies with small sample sizes.6,17 In the study by Chang et al., 74.3% of LC cases died within one year and the median survival was 7.2 months.4 Yook et al. (2022) demonstrated that 84% of the patients died after the LC diagnosis, of which 93% of them died within 10 months.9 LC-associated survival in AML and AMML cases is as low as four months.3 A 2019 cohort study shows that patients with AML and leukemia cutis are 2.06 times more likely to die than patients without skin infiltration.21 Data on CLL show that the prognosis is associated with the histological characteristics, being poor ‒ 49% survival at 2 years ‒ when there are more than 5% of large B lymphocytes in the cutaneous infiltrate and favorable – 97% survival at 2 years ‒ when there are more than 95% small B lymphocytes.16 Recent studies demonstrate that in the absence of systemic disease progression, such as for Richter's syndrome, leukemia cutis in CLL does not lead to worsening of the prognosis.15 However, the literature is still scarce and conflicting when assessing leukemia cutis and the prognosis of the underlying disease.6

Cutaneous plasmacytoma

Plasma cell dyscrasias are characterized by the clonal neoplastic expansion of cells that secrete monoclonal immunoglobulins. The clinical spectrum is diverse and groups entities of different degrees of severity, from asymptomatic monoclonal gammopathy of uncertain significance (MGUS) to malignancies of greater clinical severity, such as multiple myeloma (MM).22

Cutaneous plasmacytoma is a rare neoplasm of plasma cells that infiltrates the skin, either by direct involvement, by contiguity of a close focus, or at a distance, via a hematogenous or lymphatic route.22,23 The most often described cutaneous plasmacytomas arise in the context of MM, usually as a late complication.24 There are few reports in the literature, occurring in less than 4% of cases, although some authors believe that underdiagnosis occurs since in autopsy data of patients with MM the number of extramedullary cutaneous involvement is much higher.24–26 There is a much rarer form, primary cutaneous plasmacytoma, which occurs without evidence of another medullary or extramedullary plasma cell disease, currently classified in the group of marginal zone lymphomas. Cutaneous plasmacytomas are associated with all immunoglobulin classes, with the exception of IgE, and those related to IgG are the most frequently observed.23

The most representative clinical form is isolated, smooth, rounded erythematous-violaceous nodules (Fig. 4), but there have been descriptions of flesh-colored nodules in rare cases.26 There is no difference in the clinical picture according to the immunoglobulin involved.

Figure 4.

Cutaneous plasmacytoma. Erythematous-violaceous nodules, poorly defined and infiltrated in the periumbilical region.

(0.26MB).

Studies demonstrate that the tumor microenvironment is the main regulator of the metastatic process in the extramedullary involvement of plasma cell neoplasms, but the exact mechanism is not yet understood.26

A biopsy with histopathological and immunohistochemical analyses confirms the diagnosis. A nodular plasma cell infiltrate is the main identified pattern, followed by the interstitial one. The presence of immunoreactivity for CD138 is constant, in addition to the frequent absence of expression of CD45 and CD20.24,26

Prognosis is poor and the mean survival time is 8.5 months.24,25 Deletion of the RB1 gene has been reported to be associated with worse prognosis.24

Treatment of plasmacytomas with systemic involvement is that of the underlying disease, with or without associated radiotherapy. Primary cutaneous plasmacytomas are treated with radiotherapy alone, or by surgery followed by localized radiotherapy and/or chemotherapy.25

Secondary cutaneous lymphomas

Cutaneous lymphomas can be subdivided into two broad groups: primary, in which there is no evidence of extracutaneous disease at the time of diagnosis, and those that are secondary to systemic lymphoma.27 Primary cutaneous lymphomas (PCL) represent a heterogeneous group of entities and will not be addressed in this review.

Secondary cutaneous lymphomas (SCL) account for 20% to 50% of cutaneous lymphomas.28 They can be classified, according to the cell line that originated them, as T/NK lymphoma or B lymphoma.28 Among the reported cases of SCL in the literature, the relative frequency of the mature T/NK cell line ranged from 48% to 72% in different studies, whereas the mature B line ranged from 21% to 45%, immature hematological neoplasms corresponded to 4% to 8% of cases and Hodgkin's lymphoma accounted for 0% to 4% of cases.28–32

The clinical manifestations of SCL are polymorphic. Nodules are often present (Fig. 5) in up to 60% of cases, but macules, patches, and plaques can also occur. Ulceration occurs in up to 9% of cases. Lesion morphology did not correlate with survival in one case series.28

Figure 5.

Secondary cutaneous follicular lymphoma. (A) Brownish-erythematous, infiltrated subcutaneous tumor, with telangiectasias in the epigastric region. (B) Lesion at higher magnification.

(0.23MB).

Patients with T/NK line SCL more often manifest multiple or disseminated lesions and the presence of these lesions is a poor prognostic factor.28 Peripheral T-cell lymphomas may present clinically as nodules or tumors, but generalized maculopapular or urticarial eruptions have been described, with lesion morphology varying in the same patient over time.33

Regarding CD30+ anaplastic lymphomas, there are also significant differences between the primary cutaneous form and the secondary form. The secondary CD30+ anaplastic cutaneous lymphoma (Fig. 6) is more often characterized by papules and nodules, has a higher frequency of B symptoms, and has a worse prognosis, with higher mortality and shorter five-year survival.34

Figure 6.

Secondary cutaneous CD30+ anaplastic lymphoma – erythematous, infiltrated, raised, reddish plaque in the central portion on the posterior right axillary line.

(0.24MB).

Hodgkin's lymphoma is associated with specific cutaneous manifestations in less than 1% of cases, usually in advanced refractory disease.35 The mode of spread is by direct extension of neoplastic cells to the skin.36 Skin involvement by direct extension has also been described in high-grade nodal B lymphomas.37

The diagnosis of SCL depends on the diagnosis of the associated nodal lymphoma. The diagnosis of lymphomas is a complex one and includes clinical, morphological, histopathological, immunohistochemical, and molecular factors.38 The immunophenotype of CD20 and CD79a expression identifies B-cell line lymphomas, while the CD3 marker, as well as CD2, CD7, and LAT markers, identify the T-cell line. Other markers used for the diagnosis and classification of lymphomas are the panlymphocytic marker CD45, the NK cell marker CD56, and other cytotoxic markers for T and NK cells. Very often, only clinical, histopathological, and immunohistochemical factors are not enough to establish the diagnosis of lymphoma. In these cases, molecular methods are also used to investigate clonality and identify the cell line involved.38 To differentiate between PCL and SCL, it is necessary to perform the patient’s staging through imaging tests, bone marrow biopsy, peripheral blood flow cytometry, or other methods, aiming to assess the presence of nodal or other organ involvement at the time of diagnosis, which characterizes the SCL.

When skin involvement occurs within the first six months of diagnosis, the prognosis is worse than in cases in which these lesions occur six months after the diagnosis.28 When compared to PCL, SCL have worse five-year survival. The five-year survival for SCL is 31%, while for PCL it ranges from 87% to 92.5%.39

Treatment of SCL comprises the treatment of the nodal lymphoma that caused it. Radiotherapy alone is chosen for the localized forms or combined with chemotherapy for aggressive disease. For B-lymphomas, the anti-CD20 antibody rituximab is frequently used, together or not with multidrug chemotherapy. Other treatments used in refractory lymphomas include brentuximab vedotin, ibrutinib, acalabrutinib and idelalisib. Immunotherapy with checkpoint inhibitors has also been associated in recent years in the therapeutic arsenal used to treat lymphomas.40 Bone marrow transplantation is an alternative for refractory cases. CAR-T (chimeric antigen receptor T) cells have also shown promising results in refractory hematologic malignancies.41

Conclusion

In part I of this review, the authors demonstrate to dermatologists, hematologists, and clinicians the importance of a complete dermatological examination and familiarity with the skin alterations, which may represent a neoplastic infiltration of an already known condition or even a lesion that precedes the diagnosis of systemic disease. Etiological elucidation always needs to be confirmed by a skin biopsy with anatomopathological and immunohistochemical examination. The identification of this type of extramedullary lesion helps in the decision-making related to treatment, which, if performed early, may change prognosis.

More epidemiological work is required in this area of ​​knowledge, aiming to obtain robust and reliable statistical data. It is important to highlights the need for multidisciplinary team working for this complex type of patient, in which the dermatologist is the specialist responsible for the evaluation and diagnosis of skin alterations.

Financial support

None declared.

Authors' contributions

Patricia Karla de Souza: Design of the study; drafting of the manuscript and critical review of important intellectual content; design of the study together with the co-authors; critical review of the literature; approval of the final version of the manuscript.

Rafael Oliveira Amorim: Drafting of the manuscript and critical review of important intellectual content; design of the study together with the co-authors; critical review of the literature; approval of the final version of the manuscript.

Letícia Siqueira Sousa: Drafting of the manuscript and critical review of important intellectual content; design of the study together with the co-authors; critical review of the literature; approval of the final version of the manuscript.

Mariana Dias Batista: Drafting of the manuscript and critical review of important intellectual content; design of the study together with the co-authors; critical review of the literature; approval of the final version of the manuscript.

Conflicts of interest

None declared.

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Study conducted at the Hospital Israelita Albert Einstein, São Paulo, SP, Brazil and at the Department of Dermatology, Universidade Federal de São Paulo, São Paulo, SP, Brazil.

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