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It has several presentations and can be characterized as a hardened plaque, nodule, or vegetating lesion.<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a> Local trauma has been described as a potential risk factor for tumor onset.<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a> The most common sites of involvement are the trunk (40%–50%), the proximal limbs (30%–40%), and the head and cervical region (10%–15%). In the literature review, 11 reports of tumors located in the plantar region were retrieved. Due to the rarity of the presentation on the distal limbs, the authors believe that reporting this case is relevant.</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Case report</span><p id="par0010" class="elsevierStylePara elsevierViewall">Male patient, 35 years old, previously healthy, complained of painful lesion on the left plantar region with progressive growth over six months; he denied trauma. On physical examination, he presented an erythematous, exophytic, vegetating, and ulcerated tumor on the first metatarsal joint (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>). Histopathological examination of the lesion revealed a fusocellular proliferation with a focal storiform pattern (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>). In the immunohistochemical study, a diffuse positivity for CD34<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>cells was observed. The findings were compatible with low-grade fusocellular mesenchymal neoplasia, favoring the diagnosis of DFSP (<a class="elsevierStyleCrossRef" href="#fig0015">Fig. 3</a>). Surgical treatment involved amputation of the hallux and part of the left forefoot; no tumor recurrence was observed after four months of post-operative follow-up.</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Discussion</span><p id="par0015" class="elsevierStylePara elsevierViewall">DFSP is a rare mesenchymal tumor with low rates of aggressiveness. It presents slow progression, with high rates of local recurrence and rare cases of distant metastases. An American study conducted between 2000 and 2010 found an incidence of 41 cases in 10 million patients.<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a> Some studies observed a higher incidence in women and black people. It mostly affects the trunk (40%–50%), the proximal limbs (30%–40%), and the head and cervical region (10%–15%).<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a></p><p id="par0020" class="elsevierStylePara elsevierViewall">A literature review published in 2019 described 11 cases of dermatofibrosarcoma that affected the feet. The mean age observed was 41 years; it was more frequent in men than in women (8:3) and the most frequent location of the tumor was the dorsum of the feet. The mean growth period was 3.5 years. The mean DFSP size at diagnosis was approximately 3.5<span class="elsevierStyleHsp" style=""></span>cm. Clinical diagnosis is difficult given the variety of presentations. Dermoscopy has been described as a useful tool to aid diagnosis.<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a> In a review based on the analysis of 32 dermatofibrosarcomas, the most common features described in dermoscopy were the presence of vessels (81%), followed by a pigment network (78%) and a pinkish background (66%).<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">Histologically, dermatofibrosarcoma presents monomorphic spindle cells with little atypia and mitotic activity, arranged in irregular and multidirectional (storiform) fascicles. The tumor infiltrates the subcutaneous tissue, creating the characteristic honeycomb pattern. The histological differential diagnoses of other spindle cell tumors are dermatofibroma, malignant fibrous histiocytoma, atypical fibroxanthoma, desmoplastic melanoma, Kaposi's sarcoma, and solitary fibrous tumor.<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">Immunohistochemistry becomes an important resource for differential diagnosis, as DFSP is positive for CD34 and negative for S 100 protein, factor XIIIA, and desmin.<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a> All the cases described in the literature were tested for CD34 and were positive.<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">The recommended treatment is lesion excision with 2–3<span class="elsevierStyleHsp" style=""></span>cm of safety margins.<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a> Involvement of margins is associated with local recurrence.<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a> Another therapeutic option is Mohs micrographic surgery. Management with radiotherapy and imatinib has been described. The use of imatinib is indicated for metastases, local recurrences, as neoadjuvancy, or when the tumor is unresectable.<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">Attention should be paid to this disease, even in unusual anatomical areas, as the prognosis depends on the early diagnosis and treatment.</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Financial support</span><p id="par0045" class="elsevierStylePara elsevierViewall">None declared.</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Authors’ contributions</span><p id="par0050" class="elsevierStylePara elsevierViewall">Simone Perazzoli: Conception and planning of the study; elaboration and writing of the manuscript; critical review of the literature.</p><p id="par0055" class="elsevierStylePara elsevierViewall">Renan Rangel Bonamigo: Approval of the final version of the manuscript; conception and planning of the study; elaboration and writing of the manuscript; obtaining, analyzing, and interpreting the data; effective participation in research orientation; intellectual participation in propaedeutic and/or therapeutic conduct of studied cases; critical review of the literature; critical review of the manuscript.</p><p id="par0060" class="elsevierStylePara elsevierViewall">Renata Heck: Approval of the final version of the manuscript; conception and planning of the study; elaboration and writing of the manuscript; obtaining, analyzing, and interpreting the data; intellectual participation in propaedeutic and/or therapeutic conduct of studied cases.</p><p id="par0065" class="elsevierStylePara elsevierViewall">André da Silva Cartell: Approval of the final version of the manuscript; conception and planning of the study; intellectual participation in propaedeutic and/or therapeutic conduct of studied cases.</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Conflicts of interest</span><p id="par0070" class="elsevierStylePara elsevierViewall">None declared.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:9 [ 0 => array:3 [ "identificador" => "xres1418418" "titulo" => "Abstract" "secciones" => array:1 [ 0 => array:1 [ "identificador" => "abst0005" ] ] ] 1 => array:2 [ "identificador" => "xpalclavsec1297627" "titulo" => "Keywords" ] 2 => array:2 [ "identificador" => "sec0005" "titulo" => "Introduction" ] 3 => array:2 [ "identificador" => "sec0010" "titulo" => "Case report" ] 4 => array:2 [ "identificador" => "sec0015" "titulo" => "Discussion" ] 5 => array:2 [ "identificador" => "sec0020" "titulo" => "Financial support" ] 6 => array:2 [ "identificador" => "sec0025" "titulo" => "Authors’ contributions" ] 7 => array:2 [ "identificador" => "sec0030" "titulo" => "Conflicts of interest" ] 8 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2020-01-27" "fechaAceptado" => "2020-05-02" "PalabrasClave" => array:1 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec1297627" "palabras" => array:3 [ 0 => "Dermatofibrosarcoma" 1 => "Immunohistochemistry" 2 => "Sarcoma" ] ] ] ] "tieneResumen" => true "resumen" => array:1 [ "en" => array:2 [ "titulo" => "Abstract" "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Dermatofibrosarcoma protuberans is a rare mesenchymal tumor; it is locally aggressive and presents high rates of local recurrence. It may present as a nodular or plaque vegetating lesion. It mainly affects the trunk and proximal limbs, being rare in the distal extremities. Biopsy and immunohistochemistry help confirm the diagnosis. The authors report a case of dermatofibrosarcoma protuberans with plantar region involvement, a rare presentation. To the best of the authors’ knowledge, only 11 cases of involvement of the feet were described in the international literature.</p></span>" ] ] "NotaPie" => array:2 [ 0 => array:2 [ "etiqueta" => "⋆" "nota" => "<p class="elsevierStyleNotepara" id="npar0005">How to cite this article: Perazzoli S, Bonamigo RR, Heck R, Cartell AS. Tumor in the plantar region: dermatofibrosarcoma protuberans in an infrequent topography. An Bras Dermatol. 2020. <span class="elsevierStyleInterRef" id="intr0005" href="https://doi.org/10.1016/j.abd.2020.05.002">https://doi.org/10.1016/j.abd.2020.05.002</span></p>" ] 1 => array:2 [ "etiqueta" => "⋆⋆" "nota" => "<p class="elsevierStyleNotepara" id="npar0010">Study conducted at the Sanitary Dermatology Outpatient Clinic, Porto Alegre, RS, Brazil.</p>" ] ] "multimedia" => array:3 [ 0 => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 497 "Ancho" => 905 "Tamanyo" => 38363 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Exophytic and ulcerated tumor lesion.</p>" ] ] 1 => array:7 [ "identificador" => "fig0010" "etiqueta" => "Figure 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 716 "Ancho" => 905 "Tamanyo" => 167606 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Histopathology: fusocellular proliferation with a focal storiform pattern (Hemathoxylin & eosin ×40).</p>" ] ] 2 => array:7 [ "identificador" => "fig0015" "etiqueta" => "Figure 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 589 "Ancho" => 905 "Tamanyo" => 155903 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Immunohistochemistry: diffuse positivity for CD34 in spindle cells with storiform pattern.</p>" ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0015" "bibliografiaReferencia" => array:5 [ 0 => array:3 [ "identificador" => "bib0030" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Dermoscopy of dermatofibrosarcoma protuberans: what do we know?" 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