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brownish-yellow tumor on the left upper eyelid that was keratotic with an erythematous base&#44; which made contact with the edge of the eyelid &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The patient had no palpable locoregional lymph nodes&#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">A panoramic image &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41; revealed a neoformation with a polypoid pattern that ulcerated the entire epidermis&#46; This infiltrating tumor formed confluent nests that included some necrotic areas in the central zone&#46; Higher magnification revealed the presence of cells with moderate atypia and prominent nucleoli in the tumor nests&#46; Clear cell differentiation with a clear and finely vacuolated cytoplasm was also observed&#44; and staining was positive for carcinoembryonic antigen&#44; epithelial membrane antigen&#44; and adipophilin&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Additional Tests</span><p id="par0020" class="elsevierStylePara elsevierViewall">A full ophthalmologic examination revealed no pathological findings&#46; Blood tests and chest radiograph were normal&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">What Is Your Diagnosis&#63;</span></p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Diagnosis</span><p id="par0030" class="elsevierStylePara elsevierViewall">Sebaceous carcinoma&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Clinical Course and Treatment</span><p id="par0035" class="elsevierStylePara elsevierViewall">The lesion was removed by wedge excision with a surgical margin of 4<span class="elsevierStyleHsp" style=""></span>mm&#46; Margins were tumor-free in the histologic study&#46; A computed tomography scan of the head&#44; neck&#44; and chest revealed no evidence of locoregional or distant metastases&#46; No signs of tumor recurrence have been found during periodic follow-up over the past 2 years&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Comment</span><p id="par0040" class="elsevierStylePara elsevierViewall">Sebaceous carcinoma &#40;SC&#41; is a rare&#44; aggressive neoplasm of adnexal origin&#46; SC accounts for 0&#46;7&#37; of all skin neoplasms&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> The most common site is the upper eyelid &#40;75&#37; of cases reported&#41;&#44; although it can be found on any body part where sebaceous glands are present&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a> SC usually presents as painful yellowish-pink nodules that may clinically resemble chalazions&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">3</span></a> In rare cases&#44; it presents as a pedunculated mass resembling a cutaneous horn&#44; as in our patient&#46; Histology can show changes ranging from a well-differentiated sebaceous neoplasm with a lobular proliferation of neoplastic cells with abundant foamy cytoplasm&#8212;similar to mature sebocytes&#8212;to an undifferentiated tumor with an infiltrative growth pattern formed by neoplastic cells with marked nuclear pleomorphism&#44; a high mitotic index&#44; and a small amount of intracytoplasmic lipids&#46; Stains such as adipophilin and perilipin have shown high sensitivity and specificity for this type of neoplasm&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">4</span></a> Metastases most frequently affect the local lymph nodes &#40;preauricular&#44; parotid&#44; submandibular&#44; and cervical&#41;&#46; SC can spread through distant metastasis to organs such as the lungs&#44; liver&#44; bone&#44; and brain&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">SC can appear spontaneously or in the context of Muir-Torre syndrome&#46; This syndrome has an autosomal dominant inheritance pattern and is associated with 1 or more sebaceous skin tumors &#40;benign or malignant&#44; as in the case of SC&#41;&#44; the possible presence of keratoacanthomas&#44; and 1 or more visceral malignancies&#44; most frequently hereditary nonpolyposis colorectal cancer&#44; followed by genitourinary tumors&#46; Twenty-three percent of patients with Muir-Torre syndrome have SC&#44; so it is important to rule out this association&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Surgery is the first-line treatment for SC&#46; Because the eyelid is the most common site&#44; the first-line technique is Mohs surgery&#44;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">5&#44;6</span></a> which is associated with a lower tumor recurrence rate &#40;11&#37;&#41; than that of conventional surgery with 5 to 6<span class="elsevierStyleHsp" style=""></span>mm safety margins &#40;30&#37;&#41;&#46; Radiotherapy has been shown to be a good alternative to surgery&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">The prognosis is very unfavorable&#44; 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Case for Diagnosis
Slow-Growing Keratotic Tumor on the Eyelid
Tumor queratósico palpebral de largo tiempo de evolución
F.J. Navarro-Triviñoa,
Corresponding author
fntmed@gmail.com

Corresponding author.
, J. Aneiros-Fernándezb, A.M. Almodóvar-Realb
a Unidad de Dermatología Médico-Quirúrgica y Venereología, Hospital Universitario San Cecilio, Granada, Spain
b Servicio de Anatomía Patológica, Hospital Universitario San Cecilio, Granada, 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 47-year-old man with a past history of hepatitis C and negative human immunodeficiency virus &#40;HIV&#41; serology presented with an asymptomatic lesion on the left upper eyelid that had first appeared more than 5 years earlier&#46; The lesion began as a &#8220;pimple&#8221; and grew progressively&#46; The patient reported no exposure to toxic chemical products or to radiotherapy&#46; He had received a diagnosis of chalazion from the ophthalmology department&#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 a single&#44; well-defined&#44; brownish-yellow tumor on the left upper eyelid that was keratotic with an erythematous base&#44; which made contact with the edge of the eyelid &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The patient had no palpable locoregional lymph nodes&#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">A panoramic image &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41; revealed a neoformation with a polypoid pattern that ulcerated the entire epidermis&#46; This infiltrating tumor formed confluent nests that included some necrotic areas in the central zone&#46; Higher magnification revealed the presence of cells with moderate atypia and prominent nucleoli in the tumor nests&#46; Clear cell differentiation with a clear and finely vacuolated cytoplasm was also observed&#44; and staining was positive for carcinoembryonic antigen&#44; epithelial membrane antigen&#44; and adipophilin&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Additional Tests</span><p id="par0020" class="elsevierStylePara elsevierViewall">A full ophthalmologic examination revealed no pathological findings&#46; Blood tests and chest radiograph were normal&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">What Is Your Diagnosis&#63;</span></p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Diagnosis</span><p id="par0030" class="elsevierStylePara elsevierViewall">Sebaceous carcinoma&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Clinical Course and Treatment</span><p id="par0035" class="elsevierStylePara elsevierViewall">The lesion was removed by wedge excision with a surgical margin of 4<span class="elsevierStyleHsp" style=""></span>mm&#46; Margins were tumor-free in the histologic study&#46; A computed tomography scan of the head&#44; neck&#44; and chest revealed no evidence of locoregional or distant metastases&#46; No signs of tumor recurrence have been found during periodic follow-up over the past 2 years&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Comment</span><p id="par0040" class="elsevierStylePara elsevierViewall">Sebaceous carcinoma &#40;SC&#41; is a rare&#44; aggressive neoplasm of adnexal origin&#46; SC accounts for 0&#46;7&#37; of all skin neoplasms&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> The most common site is the upper eyelid &#40;75&#37; of cases reported&#41;&#44; although it can be found on any body part where sebaceous glands are present&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a> SC usually presents as painful yellowish-pink nodules that may clinically resemble chalazions&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">3</span></a> In rare cases&#44; it presents as a pedunculated mass resembling a cutaneous horn&#44; as in our patient&#46; Histology can show changes ranging from a well-differentiated sebaceous neoplasm with a lobular proliferation of neoplastic cells with abundant foamy cytoplasm&#8212;similar to mature sebocytes&#8212;to an undifferentiated tumor with an infiltrative growth pattern formed by neoplastic cells with marked nuclear pleomorphism&#44; a high mitotic index&#44; and a small amount of intracytoplasmic lipids&#46; Stains such as adipophilin and perilipin have shown high sensitivity and specificity for this type of neoplasm&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">4</span></a> Metastases most frequently affect the local lymph nodes &#40;preauricular&#44; parotid&#44; submandibular&#44; and cervical&#41;&#46; SC can spread through distant metastasis to organs such as the lungs&#44; liver&#44; bone&#44; and brain&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">SC can appear spontaneously or in the context of Muir-Torre syndrome&#46; This syndrome has an autosomal dominant inheritance pattern and is associated with 1 or more sebaceous skin tumors &#40;benign or malignant&#44; as in the case of SC&#41;&#44; the possible presence of keratoacanthomas&#44; and 1 or more visceral malignancies&#44; most frequently hereditary nonpolyposis colorectal cancer&#44; followed by genitourinary tumors&#46; Twenty-three percent of patients with Muir-Torre syndrome have SC&#44; so it is important to rule out this association&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Surgery is the first-line treatment for SC&#46; Because the eyelid is the most common site&#44; the first-line technique is Mohs surgery&#44;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">5&#44;6</span></a> which is associated with a lower tumor recurrence rate &#40;11&#37;&#41; than that of conventional surgery with 5 to 6<span class="elsevierStyleHsp" style=""></span>mm safety margins &#40;30&#37;&#41;&#46; Radiotherapy has been shown to be a good alternative to surgery&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">The prognosis is very unfavorable&#44; with a mortality rate of 50&#37; in the first 5 years&#46; Factors associated with poor prognosis include female sex&#44; advanced age&#44; time since onset of more than 6 months&#44; tumor size &#62;1<span class="elsevierStyleHsp" style=""></span>cm and&#44; histologically&#44; an infiltrative tumor&#44; poor differentiation&#44; vascular or perineural invasion&#44; and pagetoid dissemination&#46;</p></span></span>"
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Idiomas
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