Dermatopathology
Pigmented eccrine poroma in an atypical location
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location" "tieneTextoCompleto" => true "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "624" "paginaFinal" => "627" ] ] "autores" => array:1 [ 0 => array:4 [ "autoresLista" => "Melissa de Almeida Corrêa Alfredo, Mariana Righetto de Ré Lai, Luciane Donida Bartoli Miot, Gabriela Roncada Haddad, Aline Lutz Garcia, Hélio Amante Miot" "autores" => array:6 [ 0 => array:3 [ "nombre" => "Melissa de Almeida Corrêa" "apellidos" => "Alfredo" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] ] ] 1 => array:3 [ "nombre" => "Mariana Righetto de Ré" "apellidos" => "Lai" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] ] ] 2 => array:3 [ "nombre" => "Luciane Donida Bartoli" "apellidos" => "Miot" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] ] ] 3 => array:3 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Faculty of Medicine, Universidade Estadual Paulista, Botucatu, SP, Brazil" "etiqueta" => "b" "identificador" => "aff0010" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "Corresponding author." ] ] ] ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:8 [ "identificador" => "fig0015" "etiqueta" => "Figure 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 1414 "Ancho" => 2508 "Tamanyo" => 708306 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0075" "detalle" => "Figure " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Pigmented eccrine poroma. (A), Area with evident intratumoral melanocytes (Hematoxylin & eosin, ×100). (B), Detail of the formation of incipient intracytoplasmic lumens inside the tumor (Hematoxylin & eosin, ×400).</p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Eccrine poromas (EP) are benign neoplasms of the sweat glands consisting of epithelial cells with distal tubular differentiation (acrosyringium), representing approximately 10% of all sweat gland tumors. They are often located on the acral regions, especially the palms and soles, due to the high density of eccrine glands in these areas but can affect any region of the skin.<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Clinically, EPs present as normochromic or erythematous papules and nodules, but rarely as vegetative and ulcerative tumors. Pigmented variants are uncommon and may mimic other pigmented tumors, such as melanoma and pigmented basal cell carcinoma.<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">This report describes a young adult patient with an atypical, pigmented EP lesion on the shoulder, clinically resembling other pigmented neoplasms, emphasizing the relevance of histopathological examination for diagnostic confirmation.</p><p id="par0015" class="elsevierStylePara elsevierViewall">A 37-year-old dark-skinned male reported that he had a tumor showing progressive growth on the posterior region of the right shoulder, for one year and a half (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>A). Clinical examination disclosed a brownish vegetative tumor with a crusted surface and an infiltrated erythematous base, measuring 4 × 3 cm. Dermoscopy of the lesion showed a homogeneous image, without no structures suggestive of basal cell carcinoma or any criteria for melanocytic lesions.</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">Due to the pandemic (COVID-19), the surgical excision was delayed for one year, leading to lesion growth. Upon reassessment, the patient had a vegetative, erythematous-violaceous tumor with a blackish-brown, infiltrated surface, with a slightly erythematous base, measuring 5 × 4 cm (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>B), which gave off a foul odor. The patient had no palpable lymph node enlargement or other relevant alterations on physical examination.</p><p id="par0025" class="elsevierStylePara elsevierViewall">The lesion was submitted to total excision, with a safety margin, under the hypotheses of nodular melanoma, proliferating trichilemmal cyst, pigmented basal cell carcinoma, and pigmented dermatofibrosarcoma protuberans (Bednar's tumor).</p><p id="par0030" class="elsevierStylePara elsevierViewall">The histopathological examination revealed a well-defined nodular neoplasm, connected with the epidermis, consisting of small, monomorphic, cuboidal cells, with ample, eosinophilic cytoplasm and well-defined borders, in addition to conspicuous intercellular Bridges. There were melanin deposits diffusely distributed inside the neoplasm. Moreover, intracytoplasmic lumens and ductular formations delineated by cuticles (Figs. <a class="elsevierStyleCrossRef" href="#fig0010">2</a>‒<a class="elsevierStyleCrossRefs" href="#fig0015">4</a>) were observed in some tumor cuboidal cells. The tumor lobules did not show stromal retraction or peripheral nuclear palisading.</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><elsevierMultimedia ident="fig0020"></elsevierMultimedia><p id="par0035" class="elsevierStylePara elsevierViewall">The absence of cytological atypia, cellular pleomorphism, increased mitotic activity, and foci of necrosis corroborated the exclusion of porocarcinoma as a diagnostic possibility. Polyclonal CEA (carcinoembryonic antigen) immunostaining was negative (<a class="elsevierStyleCrossRef" href="#fig0025">Fig. 5</a>).</p><elsevierMultimedia ident="fig0025"></elsevierMultimedia><p id="par0040" class="elsevierStylePara elsevierViewall">The first EP description was reported by Pinkus et al. (1956), who described five cases of benign plantar tumors, whose histological assessment indicated a neoplasm that affected the terminal duct of the sweat glands.<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Histopathologically, EP is a benign tumor that originates in the intraepidermal portion of the sweat duct. Its etiology remains uncertain and it is a slow-growing tumor, with heterogeneous features; however, it is associated with trauma, radiation, and growth over scar tissue.<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> The acral occurrence implies a differential diagnosis, mainly with myrmecia, squamous cell carcinoma (epithelioma <span class="elsevierStyleItalic">cuniculatum</span>), pyogenic granuloma and amelanotic nodular melanoma. Surgical excision with complete removal of the neoplasm is the treatment of choice, which leads to complete healing of the lesion.</p><p id="par0050" class="elsevierStylePara elsevierViewall">The pigmented variant of EP is uncommon, corresponding to only 17% of cases, and has been previously described in individuals with different phototypes. Its diagnosis is challenging due to its rarity, and because it can be mistaken for other pigmented tumors such as melanoma, seborrheic keratosis, pigmented basal cell carcinoma, and Bednar's tumor.<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">5,6</span></a> These characteristics make histopathological analysis crucial for diagnostic confirmation and exclusion of malignancy. In these cases, there are numerous dendritic melanocytes dispersed among the tumor cells, giving the neoplasm the pigmented appearance. However, pigmented forms do not imply a different prognosis or local behavior from non-pigmented forms of EP.</p><p id="par0055" class="elsevierStylePara elsevierViewall">Eccrine porocarcinoma, which can also be pigmented, is the main differential diagnosis on histopathological examination, inasmuch as it has a slow growth, and incisional biopsies may reveal components with apparent benign characteristics, delaying the diagnosis.<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">7,8</span></a> The malignant transformation of eccrine poromas is suggested by these intratumoral findings of porocarcinomas, which indicates the removal of the entire suspicious lesion, whenever possible, for the anatomopathological study with an extensive evaluation of the neoplasm, regarding cell atypia, circumscribed architecture, mitotic activity, foci of necrosis, and cell pleomorphism.<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">9,10</span></a> Immunohistochemical demonstration of positivity with polyclonal CEA in the cytoplasm of tumor cells and in glandular lumen formations, helps in the differentiation from other epithelial neoplasms. It should be noted that negative CEA immunostaining can occur in up to 23% of porocarcinomas, especially if the monoclonal antibody is used.<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">5,11</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">Dermatologists should be aware of the diagnosis of slow-growing pigmented tumors, even outside the palms and soles, due to the possibility of a pigmented EP, a tumor with a favorable prognosis after extensive surgical excision.</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Financial support</span><p id="par0065" class="elsevierStylePara elsevierViewall">None declared.</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Authors' contributions</span><p id="par0070" class="elsevierStylePara elsevierViewall">Melissa de Almeida Corrêa Alfredo: Design and planning of the study; approval of the final version of the manuscript; critical review of the literature; critical review of the manuscript; intellectual participation in the propaedeutic and/or therapeutic conduct of the studied cases.</p><p id="par0075" class="elsevierStylePara elsevierViewall">Mariana Righetto de Ré Lai: Approval of the final version of the manuscript; critical review of the literature; critical review of the manuscript; intellectual participation in the propaedeutic and/or therapeutic conduct of the studied cases.</p><p id="par0080" class="elsevierStylePara elsevierViewall">Luciane Donida Bartoli Miot: Design and planning of the study; approval of the final version of the manuscript; critical review of the manuscript; intellectual participation in the propaedeutic and/or therapeutic conduct of the studied cases.</p><p id="par0085" class="elsevierStylePara elsevierViewall">Gabriela Roncada Haddad: Approval of the final version of the manuscript; critical review of the manuscript; intellectual participation in the propaedeutic and/or therapeutic conduct of the studied cases.</p><p id="par0090" class="elsevierStylePara elsevierViewall">Aline Lutz Garcia: Approval of the final version of the manuscript; critical review of the manuscript; intellectual participation in the propaedeutic and/or therapeutic conduct of the studied cases.</p><p id="par0095" class="elsevierStylePara elsevierViewall">Hélio Amante Miot: Approval of the final version of the manuscript; critical review of the manuscript.</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Conflicts of interest</span><p id="par0100" class="elsevierStylePara elsevierViewall">None declared.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:6 [ 0 => array:3 [ "identificador" => "xres1763869" "titulo" => "Abstract" "secciones" => array:1 [ 0 => array:1 [ "identificador" => "abst0005" ] ] ] 1 => array:2 [ "identificador" => "xpalclavsec1551038" "titulo" => "Keywords" ] 2 => array:2 [ "identificador" => "sec0005" "titulo" => "Financial support" ] 3 => array:2 [ "identificador" => "sec0010" "titulo" => "Authors' contributions" ] 4 => array:2 [ "identificador" => "sec0015" "titulo" => "Conflicts of interest" ] 5 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2021-09-14" "fechaAceptado" => "2021-10-28" "PalabrasClave" => array:1 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec1551038" "palabras" => array:3 [ 0 => "Poroma" 1 => "Neoplasms" 2 => "Skin neoplasms" ] ] ] ] "tieneResumen" => true "resumen" => array:1 [ "en" => array:2 [ "titulo" => "Abstract" "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Eccrine poroma is the term that includes benign neoplasms of the terminal duct of the eccrine sweat glands, which may clinically and dermoscopically resemble other melanoma and non-melanoma skin tumors. They are often located on the extremities (especially palms and soles), presenting as normochromic or erythematous papules and nodules, measuring up to 2 cm. Pigmented variants are uncommon, accounting for less than 20% of cases. This report describes a 37-year-old man who developed a large pigmented eccrine poroma on his right shoulder, causing diagnostic difficulty. Histopathological examination revealed a nodular neoplasm consisting of small, monomorphic, cuboidal cells, with ample, eosinophilic cytoplasm and well-defined borders, in addition to conspicuous intercellular bridges, with melanin deposits diffusely distributed inside them. The absence of cytological atypia, cellular pleomorphism, increased mitotic activity, and necrosis foci corroborated the diagnostic exclusion of porocarcinoma, which can develop from eccrine poroma.</p></span>" ] ] "NotaPie" => array:1 [ 0 => array:2 [ "etiqueta" => "☆" "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Study conducted at the Department of Dermatology, Faculty of Medicine, Universidade Estadual Paulista, Botucatu, SP, Brazil.</p>" ] ] "multimedia" => array:5 [ 0 => array:8 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1472 "Ancho" => 2508 "Tamanyo" => 424341 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0065" "detalle" => "Figure " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Pigmented eccrine poroma on the right shoulder. (A), Brownish tumor with infiltrated base, lobulated blackened areas, and crusted surface, at the first visit. (B), One year later, increase in tumor volume (5 × 4 cm), with a blackened, multilobulated appearance, and evident vegetative and exulcerated areas.</p>" ] ] 1 => array:8 [ "identificador" => "fig0010" "etiqueta" => "Figure 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 982 "Ancho" => 1675 "Tamanyo" => 359582 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0070" "detalle" => "Figure " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Pigmented eccrine poroma (Hematoxylin & eosin, ×100). Neoplasm consisting of small cuboidal cells with ample cytoplasm (smaller than the keratinocytes), with melanin deposition diffusely distributed within the neoplasm. The neoplasm is connected to the epidermis but there is no peripheral palisading.</p>" ] ] 2 => array:8 [ "identificador" => "fig0015" "etiqueta" => "Figure 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 1414 "Ancho" => 2508 "Tamanyo" => 708306 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0075" "detalle" => "Figure " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Pigmented eccrine poroma. (A), Area with evident intratumoral melanocytes (Hematoxylin & eosin, ×100). (B), Detail of the formation of incipient intracytoplasmic lumens inside the tumor (Hematoxylin & eosin, ×400).</p>" ] ] 3 => array:8 [ "identificador" => "fig0020" "etiqueta" => "Figure 4" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr4.jpeg" "Alto" => 937 "Ancho" => 1675 "Tamanyo" => 386605 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0080" "detalle" => "Figure " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Pigmented eccrine poroma (Fontana-Masson, ×100). Diffuse intratumoral deposition of melanin granules, showing a greater intensity than that of the overlying epidermis.</p>" ] ] 4 => array:8 [ "identificador" => "fig0025" "etiqueta" => "Figure 5" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr5.jpeg" "Alto" => 917 "Ancho" => 2508 "Tamanyo" => 410174 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0085" "detalle" => "Figure " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Pigmented eccrine poroma. (A), Negative immunostaining for polyclonal carcinoembryonic antigen (CEA). 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