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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Medical History</span><p id="par0005" class="elsevierStylePara elsevierViewall">A 76-year-old man presented with a slow-growing lesion that had appeared 4 years earlier on the great toe of his left foot&#46; The patient reported recurring ingrowth of the nail on the same toe prior to the appearance of the lesion&#44; as well as occasional episodes of self-limited bleeding&#46; The lesion was not painful&#44; except when the nail was ingrown or after minor trauma&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Physical Examination</span><p id="par0010" class="elsevierStylePara elsevierViewall">The lesion was a partially eroded polylobulated botryomycosis-like tumor with an indurated base and softer surface&#46; It measured approximately 3<span class="elsevierStyleHsp" style=""></span>&#215;<span class="elsevierStyleHsp" style=""></span>3<span class="elsevierStyleHsp" style=""></span>cm and covered the mid-distal part of the great toe of the left foot&#44; displacing 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">Histopathology</span><p id="par0015" class="elsevierStylePara elsevierViewall">Histopathological findings showed anastomosing cords of epithelial cells connected to the epidermis and embedded in a fibrovascular stroma&#46; The epithelial cords contained luminal cells of different sizes &#40;<a class="elsevierStyleCrossRefs" href="#fig0010">Figs&#46; 2 and 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">Additional Tests</span><p id="par0020" class="elsevierStylePara elsevierViewall">Magnetic resonance imaging disclosed a 3&#46;5<span class="elsevierStyleHsp" style=""></span>&#215;<span class="elsevierStyleHsp" style=""></span>3<span class="elsevierStyleHsp" style=""></span>&#215;<span class="elsevierStyleHsp" style=""></span>2<span class="elsevierStyleHsp" style=""></span>cm multilobulated subungual nodule confined to the soft tissue&#44; with no sign of bone destruction&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">What Is Your Diagnosis&#63;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Diagnosis</span><p id="par0030" class="elsevierStylePara elsevierViewall">Eccrine syringofibroadenoma&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Clinical Course and Treatment</span><p id="par0035" class="elsevierStylePara elsevierViewall">The lesion was excised&#44; resulting in definitive cure&#46; No recurrence has been observed to date&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Comment</span><p id="par0040" class="elsevierStylePara elsevierViewall">Eccrine syringofibroadenoma &#40;ESFA&#41; is a rare tumor that was described by Mascar&#243; in 1963&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Clinical presentation varies&#44; ranging from solitary lesions to multiple papules and nodules&#46; The clinical classification Starink<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> proposed in 1997 named 4 subtypes&#58; solitary ESFA&#44; multiple ESFA as a marker of the Sch&#246;pf syndrome &#40;ectodermal dysplasia&#41;&#44; multiple ESFA with no associated skin findings&#44; and nonhereditary unilateral linear ESFA &#40;also referred to as unilateral linear nevoid syringofibroadenoma&#41;&#46; Solitary ESFA&#44; the most common type&#44; usually forms in the distal region of the limbs&#46; Histologically&#44; the tumor is composed of thin cords and strands of epithelial cells in a network connected to the epidermis&#46; Cells are paler than epidermal keratinocytes and luminal cells surrounded by an eosinophilic cuticle can often be found within cords&#46; A highly fibrovascular stroma lies between the strands and the cords&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> The histologic&#44; ultrastructural&#44; and immunohistochemical features reported in the literature suggest that this tumor has an acrosyringeal and eccrine intradermal ductal nature&#46;<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#8211;6</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">The pathogenesis of solitary ESFA is poorly understood&#46; Some authors suggest that it is not a true benign neoplasm of the eccrine glands but rather reactive hyperplasia of the eccrine ducts as a response to repeated tissue damage &#40;chronic ulcers&#44; chronic lymphedema&#44; burns&#44; nail trauma&#44; etc&#46;&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> In this context&#44; a new reactive subtype of solitary ESFA has been proposed&#46;<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#8211;6</span></a> Our case&#44; in which the lesion developed secondary to repeated ingrowth of the toenail&#44; 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Case for diagnosis
Tumor on the Great Toe of the Left Foot
Tumoración en el primer dedo del pie izquierdo
J. Bernat-García
Corresponding author
josefabernat@hotmail.com

Corresponding Author.
, A. Mateu- Puchades, A. Marquina-Vila
Servicio Dermatología, Hospital Universitario Doctor Peset, Valencia, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Medical History</span><p id="par0005" class="elsevierStylePara elsevierViewall">A 76-year-old man presented with a slow-growing lesion that had appeared 4 years earlier on the great toe of his left foot&#46; The patient reported recurring ingrowth of the nail on the same toe prior to the appearance of the lesion&#44; as well as occasional episodes of self-limited bleeding&#46; The lesion was not painful&#44; except when the nail was ingrown or after minor trauma&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Physical Examination</span><p id="par0010" class="elsevierStylePara elsevierViewall">The lesion was a partially eroded polylobulated botryomycosis-like tumor with an indurated base and softer surface&#46; It measured approximately 3<span class="elsevierStyleHsp" style=""></span>&#215;<span class="elsevierStyleHsp" style=""></span>3<span class="elsevierStyleHsp" style=""></span>cm and covered the mid-distal part of the great toe of the left foot&#44; displacing 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">Histopathology</span><p id="par0015" class="elsevierStylePara elsevierViewall">Histopathological findings showed anastomosing cords of epithelial cells connected to the epidermis and embedded in a fibrovascular stroma&#46; The epithelial cords contained luminal cells of different sizes &#40;<a class="elsevierStyleCrossRefs" href="#fig0010">Figs&#46; 2 and 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">Additional Tests</span><p id="par0020" class="elsevierStylePara elsevierViewall">Magnetic resonance imaging disclosed a 3&#46;5<span class="elsevierStyleHsp" style=""></span>&#215;<span class="elsevierStyleHsp" style=""></span>3<span class="elsevierStyleHsp" style=""></span>&#215;<span class="elsevierStyleHsp" style=""></span>2<span class="elsevierStyleHsp" style=""></span>cm multilobulated subungual nodule confined to the soft tissue&#44; with no sign of bone destruction&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">What Is Your Diagnosis&#63;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Diagnosis</span><p id="par0030" class="elsevierStylePara elsevierViewall">Eccrine syringofibroadenoma&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Clinical Course and Treatment</span><p id="par0035" class="elsevierStylePara elsevierViewall">The lesion was excised&#44; resulting in definitive cure&#46; No recurrence has been observed to date&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Comment</span><p id="par0040" class="elsevierStylePara elsevierViewall">Eccrine syringofibroadenoma &#40;ESFA&#41; is a rare tumor that was described by Mascar&#243; in 1963&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Clinical presentation varies&#44; ranging from solitary lesions to multiple papules and nodules&#46; The clinical classification Starink<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> proposed in 1997 named 4 subtypes&#58; solitary ESFA&#44; multiple ESFA as a marker of the Sch&#246;pf syndrome &#40;ectodermal dysplasia&#41;&#44; multiple ESFA with no associated skin findings&#44; and nonhereditary unilateral linear ESFA &#40;also referred to as unilateral linear nevoid syringofibroadenoma&#41;&#46; Solitary ESFA&#44; the most common type&#44; usually forms in the distal region of the limbs&#46; Histologically&#44; the tumor is composed of thin cords and strands of epithelial cells in a network connected to the epidermis&#46; Cells are paler than epidermal keratinocytes and luminal cells surrounded by an eosinophilic cuticle can often be found within cords&#46; A highly fibrovascular stroma lies between the strands and the cords&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> The histologic&#44; ultrastructural&#44; and immunohistochemical features reported in the literature suggest that this tumor has an acrosyringeal and eccrine intradermal ductal nature&#46;<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#8211;6</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">The pathogenesis of solitary ESFA is poorly understood&#46; Some authors suggest that it is not a true benign neoplasm of the eccrine glands but rather reactive hyperplasia of the eccrine ducts as a response to repeated tissue damage &#40;chronic ulcers&#44; chronic lymphedema&#44; burns&#44; nail trauma&#44; etc&#46;&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> In this context&#44; a new reactive subtype of solitary ESFA has been proposed&#46;<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#8211;6</span></a> Our case&#44; in which the lesion developed secondary to repeated ingrowth of the toenail&#44; could be considered a reactive ESFA&#46; Recent reports have described cases of solitary ESFA associated with squamous cell carcinoma and the malignant transformation of solitary ESFA&#46; Histologically&#44; this diagnosis must be differentiated from fibroepithelioma of Pinkus&#44; tumors of the follicular infundibulum&#44; and squamous cell carcinoma&#46; Solitary ESFA is treated according to the number&#44; site&#44; and resectability of the lesions&#44; and simple excision is the treatment of choice in solitary tumors&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a></p></span></span>"
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