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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 57-year-old male farmer with no relevant personal or family medical history and no known diseases presented with a lesion on the inner aspect of the left leg that had appeared about 10 years previously&#46; The lesion was asymptomatic&#44; had never bled&#44; and had slowly and progressively grown over the years&#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 exophytic&#44; polypoid tumor with a broad base and no adhesion to the deeper layers&#46; The tumor was soft with a friable&#44; erythematous&#44; fleshy surface and measured 3<span class="elsevierStyleHsp" style=""></span>cm in diameter &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Dermoscopy revealed that the tumor surface consisted of multiple raised structures interconnected in a honeycomb pattern and displayed some whitish radial streaks and fine arborizing telangiectasias &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">Locoregional lymph nodes were not palpable and no other significant abnormalities were observed in the physical examination&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Histopathology</span><p id="par0025" class="elsevierStylePara elsevierViewall">Histopathology with hematoxylin-eosin &#40;original magnification &#215;<span class="elsevierStyleHsp" style=""></span>20&#41; revealed a tumor composed of thin&#44; elongated&#44; anastamosing strands of basaloid cells that were connected to the epidermis and extended down towards the dermis forming a lattice-like pattern within a dense fibrotic stroma &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0030" class="elsevierStylePara elsevierViewall">What Is Your Diagnosis&#63;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Diagnosis</span><p id="par0035" class="elsevierStylePara elsevierViewall">Fibroepithelioma of Pinkus&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Clinial Course and Treatment</span><p id="par0040" class="elsevierStylePara elsevierViewall">Under local anesthesia&#44; the patient underwent surgical excision with margins and direct closure&#44; without complications&#46; After 6 months of follow-up the patient has a nonpathological scar with no signs of local recurrence or new lesions&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Comment</span><p id="par0045" class="elsevierStylePara elsevierViewall">Fibroepithelioma of Pinkus&#44; initially described in 1953 as a premalignant fibroepithelial tumor of the skin&#44;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> is a benign neoplasm with differentiation toward follicular germinative cells&#46; This tumor has been traditionally considered a rare variant of basal cell carcinoma &#40;BCC&#41;&#44; based on its characteristic histopathological features&#46; Histologically&#44; the tumor consists of strands of interconnected basaloid epithelia coated with preexisting follicular infundibula that connect to the epidermis to form a fenestrated pattern&#44; with occasional solid islands of basaloid cells&#44; a dense fibrotic stroma&#44; and a rich capillary network&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> In some cases the cytology&#44; stroma&#44; and architectural features suggest that this tumor type would be more correctly classified as a retiform variant of trichoblastoma rather than a BCC&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> However&#44; it does not display as advanced a degree of follicular differentiation as seen in trichoblastoma&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Fibroepithelioma of Pinkus affects men and women similarly&#44; and appears in individuals between 40 and 60 years of age&#46; The most common location is the trunk&#46; It has a predilection for unexposed areas &#40;unlike BCC&#41;&#44; especially the lumbosacral area&#44; although it can develop in any anatomic site except areas of skin that lack hair follicles&#46; While the tumor manifests clinically as an initially flat lesion&#44; it grows progressively and causes few symptoms&#44; and can thus reach a large size&#44; as seen in our patient&#46; It is scarcely aggressive and has a good prognosis&#59; no distant metastases have been described&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">The dermoscopic pattern of this tumor has been described&#59; the key features are arborized telangiectasias that are longer and finer than those seen in BCC and whitish streaks caused by abundant fibrovascular stroma&#46; These correspond respectively to the brownish maple leaf and spoke-wheel structures seen in classic BCC&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">The differential diagnosis of Fibroepithelioma of Pinkus includes squamous cell carcinoma&#44; amelanotic melanoma&#44; skin metastasis&#44; Merkel cell carcinoma&#44; and primary cutaneous diffuse large B-cell lymphoma&#44; leg type&#46; 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Case for Diagnosis
A Slow-Growing Pedunculated Lesion
Lesión pediculada de crecimiento lento
M.T. López-Villaescusa
Autor para correspondencia
lopezvillaescusa@hotmail.com

Corresponding author.
, F. de Manueles Marcos, L.J. Pérez García
Servicio de Dermatología, Complejo Hospitalario Universitario de Albacete, Albacete, Spain
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1</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Dermoscopy revealed that the tumor surface consisted of multiple raised structures interconnected in a honeycomb pattern and displayed some whitish radial streaks and fine arborizing telangiectasias &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">Locoregional lymph nodes were not palpable and no other significant abnormalities were observed in the physical examination&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Histopathology</span><p id="par0025" class="elsevierStylePara elsevierViewall">Histopathology with hematoxylin-eosin &#40;original magnification &#215;<span class="elsevierStyleHsp" style=""></span>20&#41; revealed a tumor composed of thin&#44; elongated&#44; anastamosing strands of basaloid cells that were connected to the epidermis and extended down towards the dermis forming a lattice-like pattern within a dense fibrotic stroma &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0030" class="elsevierStylePara elsevierViewall">What Is Your Diagnosis&#63;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Diagnosis</span><p id="par0035" class="elsevierStylePara elsevierViewall">Fibroepithelioma of Pinkus&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Clinial Course and Treatment</span><p id="par0040" class="elsevierStylePara elsevierViewall">Under local anesthesia&#44; the patient underwent surgical excision with margins and direct closure&#44; without complications&#46; After 6 months of follow-up the patient has a nonpathological scar with no signs of local recurrence or new lesions&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Comment</span><p id="par0045" class="elsevierStylePara elsevierViewall">Fibroepithelioma of Pinkus&#44; initially described in 1953 as a premalignant fibroepithelial tumor of the skin&#44;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> is a benign neoplasm with differentiation toward follicular germinative cells&#46; This tumor has been traditionally considered a rare variant of basal cell carcinoma &#40;BCC&#41;&#44; based on its characteristic histopathological features&#46; Histologically&#44; the tumor consists of strands of interconnected basaloid epithelia coated with preexisting follicular infundibula that connect to the epidermis to form a fenestrated pattern&#44; with occasional solid islands of basaloid cells&#44; a dense fibrotic stroma&#44; and a rich capillary network&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> In some cases the cytology&#44; stroma&#44; and architectural features suggest that this tumor type would be more correctly classified as a retiform variant of trichoblastoma rather than a BCC&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> However&#44; it does not display as advanced a degree of follicular differentiation as seen in trichoblastoma&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Fibroepithelioma of Pinkus affects men and women similarly&#44; and appears in individuals between 40 and 60 years of age&#46; The most common location is the trunk&#46; It has a predilection for unexposed areas &#40;unlike BCC&#41;&#44; especially the lumbosacral area&#44; although it can develop in any anatomic site except areas of skin that lack hair follicles&#46; While the tumor manifests clinically as an initially flat lesion&#44; it grows progressively and causes few symptoms&#44; and can thus reach a large size&#44; as seen in our patient&#46; It is scarcely aggressive and has a good prognosis&#59; no distant metastases have been described&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">The dermoscopic pattern of this tumor has been described&#59; the key features are arborized telangiectasias that are longer and finer than those seen in BCC and whitish streaks caused by abundant fibrovascular stroma&#46; These correspond respectively to the brownish maple leaf and spoke-wheel structures seen in classic BCC&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">The differential diagnosis of Fibroepithelioma of Pinkus includes squamous cell carcinoma&#44; amelanotic melanoma&#44; skin metastasis&#44; Merkel cell carcinoma&#44; and primary cutaneous diffuse large B-cell lymphoma&#44; leg type&#46; However&#44; those tumors are malignant skin neoplasms characterized by rapid growth and a poor prognosis&#44; features that are not concordant with the clinical course of our patient&#39;s tumor&#46; Therefore&#44; the differential diagnosis must also include other less common benign neoplasms with follicular differentiation in which the definitive diagnosis is established by histopathology&#59; these include large solitary trichodiscoma&#44; trichoadenoma&#44; fibroadenoma&#44; and eccrine syringofibroadenoma&#44; as well as other tumors such as lymphoepithelial tumor of the skin&#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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