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1</a>&#41;&#46; Palpation was painless and the lesion didn¿t disappear with vitropression&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Histopathology</span><p id="par0015" class="elsevierStylePara elsevierViewall">The histopathologic examination of an excisional biopsy showed a band like proliferation of fusiform cells&#44; in a parallel distribution&#44; seated on the papillary and upper reticular dermis&#44; with no spreading to the subcutaneous tissue&#46; Mitoses were rare and adnexal structures&#44; nerves&#44; and vessels were preserved &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Immunohistochemical staining demonstrated that these cells were CD34 positive&#44; and factor XIIIa and S100 negative &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Diagnosis</span><p id="par0020" class="elsevierStylePara elsevierViewall">Taken together&#44; the morphologic and immunophenotypic findings were felt to be most consistent with plaque-like CD34-positive dermal fibroma&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Course and treatment</span><p id="par0025" class="elsevierStylePara elsevierViewall">Excisional biopsy was the offered treatment without any complication&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Comment</span><p id="par0030" class="elsevierStylePara elsevierViewall">Medallion-like dermal dendrocyte hamartoma &#40;MDDH&#41; also known as plaque-like CD34-positive dermal fibroma &#40;PDF&#41; was first described by Rodriguez-Jurado et al in 2004&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a> The initial doubling of terminology has been elucidated as studies have suggested that the lesion neither is a hamartoma nor possess dermal dendrocytic differentiation&#46; For these reasons&#44; Kutzner and colleagues have suggested an adjustment in nomenclature to PDF&#44; widening the spectrum of this tumor&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">PDF is a rare&#44; benign&#44; spindle cell neoplasm that classically presents as a congenital&#44; asymptomatic&#44; solitary&#44; round- or triangular-shaped patch&#47;plaque&#44; on the neck or trunk&#44; and most commonly in females&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">3&#44;4</span></a> The overlying skin may be pink to brown&#44; finely wrinkled&#44; and&#47;or atrophic&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a> With the new nomenclature other cases were described&#44; and this description has included congenital and acquired tumors&#44; lesions located in different body sites rather than neck or trunk and also lacking the typical presentation&#46; In fact&#44; there are reports of lesions located on the limbs&#44; hands and feet and also cases of indurated and angiomatous plaques&#44; dermal nodules and pedunculated lesions&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">4&#44;5</span></a> Our case represents an acquired form&#44; however clinically very similar to the classical presentation&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Given its clinical heterogeneity&#44; PDF may be clinically misdiagnosed as&#58; congenital nevus&#59; fibroblastic connective tissue nevus&#59; neurofibroma&#59; dermatofibroma&#59; dermatomyofibroma&#59; anetoderma&#59; aplasia cutis&#59; or&#44; most importantly&#44; as dermatofibrosarcoma protuberans &#40;DFSP&#41;&#46; It is critical to make the distinction between DFSP and PDF to prevent unnecessary wide excisions&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Histology is characterized by a band-like dermal proliferation of spindle cells&#44; which strongly express CD34&#46; For this reason&#44; the major differential diagnosis is with DFSP&#46; Thus&#44; it is important to fully characterize its histological and immunohistochemical findings and sometimes add cytogenetic and molecular studies when face with difficult or borderline cases&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a> Immunohistochemically&#44; the neoplastic cells are positive for CD34 and show variable expression of factor XIIIa and are negative for melanocytic markers &#40;S100&#44; MelanA&#44; HMB45&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">We feel our case description is another example of a PDF&#46; This case included&#44; 21 occurrences of this rare neoplasm have been reported so far&#46; Despite their histopathologic similarities&#44; they have revealed an appreciable variability in clinical features&#46; 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Case for Diagnosis
A Flat Pink Plaque On The Right Anterior Forearm
Placa de color rosa en superficie anterior de antebrazo derecho
S. Campos
Autor para correspondencia
saraazevedocampos@gmail.com

Corresponding author.
, A. João, A. Lencastre
Unidad de Dermato-Venereología, Centro Hospitalar Lisboa Central, Hospital Santo António dos Capuchos, Lisboa, Portugal
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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Case history</span><p id="par0005" class="elsevierStylePara elsevierViewall">A 32-year-old healthy Caucasian woman presented with a solitary&#44; asymptomatic lesion on the right anterior forearm&#46; She had first noticed this lesion 4 years earlier and hadn¿t related with nothing in particular&#59; she also denied subsequent changes in size or appearance&#46; She had no history of personal or family diseases&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Physical examination</span><p id="par0010" class="elsevierStylePara elsevierViewall">Physical examination revealed an oval&#44; pink to brown&#44; smooth yet finely wrinkled plaque&#44; measuring 12x6<span class="elsevierStyleHsp" style=""></span>mm &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; Palpation was painless and the lesion didn¿t disappear with vitropression&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Histopathology</span><p id="par0015" class="elsevierStylePara elsevierViewall">The histopathologic examination of an excisional biopsy showed a band like proliferation of fusiform cells&#44; in a parallel distribution&#44; seated on the papillary and upper reticular dermis&#44; with no spreading to the subcutaneous tissue&#46; Mitoses were rare and adnexal structures&#44; nerves&#44; and vessels were preserved &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Immunohistochemical staining demonstrated that these cells were CD34 positive&#44; and factor XIIIa and S100 negative &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Diagnosis</span><p id="par0020" class="elsevierStylePara elsevierViewall">Taken together&#44; the morphologic and immunophenotypic findings were felt to be most consistent with plaque-like CD34-positive dermal fibroma&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Course and treatment</span><p id="par0025" class="elsevierStylePara elsevierViewall">Excisional biopsy was the offered treatment without any complication&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Comment</span><p id="par0030" class="elsevierStylePara elsevierViewall">Medallion-like dermal dendrocyte hamartoma &#40;MDDH&#41; also known as plaque-like CD34-positive dermal fibroma &#40;PDF&#41; was first described by Rodriguez-Jurado et al in 2004&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a> The initial doubling of terminology has been elucidated as studies have suggested that the lesion neither is a hamartoma nor possess dermal dendrocytic differentiation&#46; For these reasons&#44; Kutzner and colleagues have suggested an adjustment in nomenclature to PDF&#44; widening the spectrum of this tumor&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">PDF is a rare&#44; benign&#44; spindle cell neoplasm that classically presents as a congenital&#44; asymptomatic&#44; solitary&#44; round- or triangular-shaped patch&#47;plaque&#44; on the neck or trunk&#44; and most commonly in females&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">3&#44;4</span></a> The overlying skin may be pink to brown&#44; finely wrinkled&#44; and&#47;or atrophic&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a> With the new nomenclature other cases were described&#44; and this description has included congenital and acquired tumors&#44; lesions located in different body sites rather than neck or trunk and also lacking the typical presentation&#46; In fact&#44; there are reports of lesions located on the limbs&#44; hands and feet and also cases of indurated and angiomatous plaques&#44; dermal nodules and pedunculated lesions&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">4&#44;5</span></a> Our case represents an acquired form&#44; however clinically very similar to the classical presentation&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Given its clinical heterogeneity&#44; PDF may be clinically misdiagnosed as&#58; congenital nevus&#59; fibroblastic connective tissue nevus&#59; neurofibroma&#59; dermatofibroma&#59; dermatomyofibroma&#59; anetoderma&#59; aplasia cutis&#59; or&#44; most importantly&#44; as dermatofibrosarcoma protuberans &#40;DFSP&#41;&#46; It is critical to make the distinction between DFSP and PDF to prevent unnecessary wide excisions&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Histology is characterized by a band-like dermal proliferation of spindle cells&#44; which strongly express CD34&#46; For this reason&#44; the major differential diagnosis is with DFSP&#46; Thus&#44; it is important to fully characterize its histological and immunohistochemical findings and sometimes add cytogenetic and molecular studies when face with difficult or borderline cases&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a> Immunohistochemically&#44; the neoplastic cells are positive for CD34 and show variable expression of factor XIIIa and are negative for melanocytic markers &#40;S100&#44; MelanA&#44; HMB45&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">We feel our case description is another example of a PDF&#46; This case included&#44; 21 occurrences of this rare neoplasm have been reported so far&#46; Despite their histopathologic similarities&#44; they have revealed an appreciable variability in clinical features&#46; These differences have been related to the onset of the lesion &#40;congenital or acquired&#41;&#44; patient age at presentation&#44; gender&#44; location and specific clinical characteristics&#44; and positivity to Factor XIIIa&#46; Bearing this in mind&#44; it is important to determine whether all apparent clinical variants are distinct subtypes of one same neoplasm or rather represent unique CD34-positive spindle cell proliferations&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">Although a spectrum of this entity is still being defined&#44; PDF should always be considered within the differential diagnosis of CD34-positive dermal spindle cell neoplasms&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a></p></span></span>"
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        "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as&#58; Campos S&#44; Jo&#227;o A&#44; Lencastre A&#46; Placa de color rosa en superficie anterior de antebrazo derecho&#46; Actas Dermosifiliogr&#46; 2018&#59;109&#58;823&#8211;824&#46;</p>"
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