D. Sachdev, R. Barnhill, E. Taylor, S. Worswick
{"title":"Cellular Neurothekeoma in a Female with Guillain-Barré Syndrome: A Case Report and Review of the Literature","authors":"D. Sachdev, R. Barnhill, E. Taylor, S. Worswick","doi":"10.1159/000369162","DOIUrl":null,"url":null,"abstract":"Cellular neurothekeoma is a rare cutaneous tumor that occurs more frequently in women. A 68-year-old female with a history of left nasal alar basal cell carcinoma and Guillain-Barré syndrome presented to the clinic with a 3-mm firm skin-colored papule with scattered telangiectasias. Histopathologic examination with immunochemistry of the lesion was consistent with cellular neurothekeoma. It stained positive for microphthalmia transcription factor and NKI-C3 and negative for HMB-45 and S-100. The lesion was excised with 3-mm margins, and no recurrence was noted within 1 year of follow-up. We present a case of cellular neurothekeoma in a patient with a history of Guillain-Barré syndrome as well as a review of the literature. Our case report is unique in that no prior association has been found in the literature between cellular neurothekeoma and Guillain-Barré syndrome. © 2014 S. Karger AG, Basel","PeriodicalId":42885,"journal":{"name":"Dermatopathology","volume":"1 1","pages":"91 - 97"},"PeriodicalIF":1.6000,"publicationDate":"2014-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000369162","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dermatopathology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1159/000369162","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"DERMATOLOGY","Score":null,"Total":0}
引用次数: 3
女性格林-巴勒综合征的细胞性神经瘤1例报告及文献复习
细胞性神经瘤是一种罕见的皮肤肿瘤,多见于女性。一位68岁女性,有左鼻翼基底细胞癌和格林-巴-罗综合征的病史,就诊时出现一个3毫米厚的皮肤色硬丘疹,伴有分散的毛细血管扩张。组织病理及免疫化学检查符合细胞性神经瘤。小眼转录因子和NKI-C3阳性,HMB-45和S-100阴性。病灶以3mm边缘切除,随访1年无复发。我们提出一个病例的细胞神经瘤患者与格林-巴-罗综合征的历史,以及文献综述。我们的病例报告是独一无二的,因为在文献中没有发现细胞性神经瘤和格林-巴列综合征之间的关联。©2014 S. Karger AG,巴塞尔
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