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2</a>B&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">Immunohistochemistry was positive for CD34 only in the vascular component of the tumor and was negative for S-100 protein&#44; epithelial membrane antigen&#44; and MUC4 in the vascular component and the fibroblastic component&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">What Is Your Diagnosis</span>&#63;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Diagnosis</span><p id="par0030" class="elsevierStylePara elsevierViewall">Subungual superficial angiomyxoma&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Clinical Course and Treatment</span><p id="par0035" class="elsevierStylePara elsevierViewall">After excision of the subungueal tumor we performed a direct suture closure&#46; 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skin pigmentation&#44; or endocrine alterations&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">Superficial angiomyxoma is more common in men&#44; usually between 20 and 50 years of age&#46; It normally appears as a single lesion<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> and has a very heterogeneous clinical presentation&#46; The lesion presents as a skin-colored papule&#44; nodule&#44; or polypoid lesion ranging from 1 to 5<span class="elsevierStyleHsp" style=""></span>cm in size&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> The most common site in the reported series is the trunk&#44; followed by the lower limbs and head or neck&#46;<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#44;5</span></a> It is very rare to find this lesion in a subungueal site&#44; as in our patient&#46; Only 3 cases of subungueal superficial angiomyxoma have been reported&#46;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6&#44;7</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">Histologically&#44; superficial angiomyxoma is a dermal tumor that extends into the subcutaneous tissue&#46; The lesion usually presents a multi-lobed growth pattern with nodules of low cellularity immersed in a myxoid stroma&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;4&#44;5</span></a> It contains cells of fibroblast morphology with fusiform&#44; elongated&#44; or stellate shapes that do not usually present atypia or mitotic figures&#46; The presence of abundant vessels with narrow lumens is characteristic&#44; and a perivascular neutrophilic and lymphocytic inflammatory infiltrate is seen in a third of cases&#46; Immunohistochemical features of the lesions are fibroblast cells that are negative for CD34&#44; smooth muscle actin&#44; S-100 protein&#44; epithelial membrane antigen&#44; and desmin&#59; however&#44; myofibroblast differentiation may be present in some cases&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;3</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">For subungueal lesions&#44;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6&#44;7</span></a> the main differential diagnosis is superficial acral fibromyxoma&#44; a slow-growing benign tumor usually found on the toes and fingers&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> Histologically&#44; this lesion presents as a well-defined dermal tumor that&#44; in contrast to superficial angiomyxoma&#44; has a less abundant myxoid stroma&#44; higher cell density&#44; increased microvascularization&#44; and less prominent capillaries&#46; Immunohistochemically&#44; the lesion is characterized by CD34 expression in fibroblasts&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> In our patient&#44; immunohistochemistry was negative for CD34 in the spindle-shaped fibroblastic component&#46;</p><p id="par0060" class="elsevierStylePara elsevierViewall">Superficial angiomyxoma is treated by surgery and local recurrences occur in 30&#37; to 40&#37; of cases&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;3&#44;5</span></a> The lesion is considered to be a benign myxoid tumor&#46; No metastatic cases have been reported to date&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Conflicts of Interest</span><p id="par0065" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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CASE FOR DIAGNOSIS
Hyperkeratotic Subungual Tumor
Lesión tumoral hiperqueratósica subungueal
D. Ayalaa,
Autor para correspondencia
dayalca83@hotmail.com

Corresponding author.
, V. Pugliab, E. Jordáa
a Servicio de Dermatología, Hospital Clínico Universitario de Valencia, Valencia, Spain
b Servicio de Anatomía Patológica, Hospital Clínico Universitario de Valencia, Valencia, Spain
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hyperkeratotic surface that was causing the detachment of the nail &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Additional Tests</span><p id="par0015" class="elsevierStylePara elsevierViewall">Complete excision of the lesion was performed&#46; Histopathologic examination revealed a diffuse unencapsulated dermal lesion that extended to the deep margin of the resection specimen &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>A&#41;&#46; The tumor contained a prominent myxoid stroma with low cellularity consisting of spindle-shaped cells&#44; without atypia or mitotic figures&#46; A vascular network of numerous elongated capillaries with narrow lumens was present&#46; No inflammatory infiltrate was observed &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>B&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">Immunohistochemistry was positive for CD34 only in the vascular component of the tumor and was negative for S-100 protein&#44; epithelial membrane antigen&#44; and MUC4 in the vascular component and the fibroblastic component&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">What Is Your Diagnosis</span>&#63;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Diagnosis</span><p id="par0030" class="elsevierStylePara elsevierViewall">Subungual superficial angiomyxoma&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Clinical Course and Treatment</span><p id="par0035" class="elsevierStylePara elsevierViewall">After excision of the subungueal tumor we performed a direct suture closure&#46; Because the deep margin of the resected specimen was affected&#44; we initially considered extending the surgical margins&#46; However&#44; the patient refused additional surgery and no evidence of tumor recurrence has been found during 12 months of follow-up&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Comment</span><p id="par0040" class="elsevierStylePara elsevierViewall">Superficial angiomyxoma is a rare mesenchymal tumor classified as a benign cutaneous myxoma&#46; It was first described by Carney et al&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> as being associated with Carney complex&#46; It is mainly necessary to rule out Carney syndrome in patients with superficial angiomyxomas on the outer ear and patients with multiple lesions&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> We determined that our patient did not have Carney syndrome because the subungueal tumor was not accompanied by extracutaneous myxomas&#44; skin pigmentation&#44; or endocrine alterations&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">Superficial angiomyxoma is more common in men&#44; usually between 20 and 50 years of age&#46; It normally appears as a single lesion<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> and has a very heterogeneous clinical presentation&#46; The lesion presents as a skin-colored papule&#44; nodule&#44; or polypoid lesion ranging from 1 to 5<span class="elsevierStyleHsp" style=""></span>cm in size&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> The most common site in the reported series is the trunk&#44; followed by the lower limbs and head or neck&#46;<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#44;5</span></a> It is very rare to find this lesion in a subungueal site&#44; as in our patient&#46; Only 3 cases of subungueal superficial angiomyxoma have been reported&#46;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6&#44;7</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">Histologically&#44; superficial angiomyxoma is a dermal tumor that extends into the subcutaneous tissue&#46; The lesion usually presents a multi-lobed growth pattern with nodules of low cellularity immersed in a myxoid stroma&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;4&#44;5</span></a> It contains cells of fibroblast morphology with fusiform&#44; elongated&#44; or stellate shapes that do not usually present atypia or mitotic figures&#46; The presence of abundant vessels with narrow lumens is characteristic&#44; and a perivascular neutrophilic and lymphocytic inflammatory infiltrate is seen in a third of cases&#46; Immunohistochemical features of the lesions are fibroblast cells that are negative for CD34&#44; smooth muscle actin&#44; S-100 protein&#44; epithelial membrane antigen&#44; and desmin&#59; however&#44; myofibroblast differentiation may be present in some cases&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;3</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">For subungueal lesions&#44;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6&#44;7</span></a> the main differential diagnosis is superficial acral fibromyxoma&#44; a slow-growing benign tumor usually found on the toes and fingers&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> Histologically&#44; this lesion presents as a well-defined dermal tumor that&#44; in contrast to superficial angiomyxoma&#44; has a less abundant myxoid stroma&#44; higher cell density&#44; increased microvascularization&#44; and less prominent capillaries&#46; Immunohistochemically&#44; the lesion is characterized by CD34 expression in fibroblasts&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> In our patient&#44; immunohistochemistry was negative for CD34 in the spindle-shaped fibroblastic component&#46;</p><p id="par0060" class="elsevierStylePara elsevierViewall">Superficial angiomyxoma is treated by surgery and local recurrences occur in 30&#37; to 40&#37; of cases&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;3&#44;5</span></a> The lesion is considered to be a benign myxoid tumor&#46; No metastatic cases have been reported to date&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Conflicts of Interest</span><p id="par0065" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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