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首页> 外文期刊>American Journal of Dermatopathology >Primary adenoid cystic carcinoma of the skin metastatic to the lymph nodes: immunohistochemical study of a new case and literature review.
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Primary adenoid cystic carcinoma of the skin metastatic to the lymph nodes: immunohistochemical study of a new case and literature review.

机译:皮肤原发性腺样囊性癌转移至淋巴结:一例新的免疫组织化学研究及文献综述。

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摘要

Primary cutaneous adenoid cystic carcinoma (PCACC) is a rare adnexal skin tumor first described in 1975, of which merely 62 cases have so far been studied in detail and reported in the English literature. PCACC is usually regarded as apocrine in origin/differentiation, but its precise histogenesis is still not well known. PCACC has in most cases a rather indolent course but can produce local recurrences and, more rarely, regional (lymph node) and distant (pulmonary) metastases. We report herein a Greek woman with a long-standing PCACC that grew slowly over several years and produced metastasis in the regional lymph nodes, highlighting the potentially aggressive course of this tumor. The primary and metastatic tumors were studied immunohistochemically and proved to express several (sweat gland-related) antigens (such as keratin 7, epithelial membrane antigen, CD10, and CD117) but neither hormonal receptors nor p63 or Gross Cystic disease Fluid Protein 15. The salient clinicopathologic features of this rare cutaneous adnexal tumor are reviewed.
机译:原发性皮肤腺样囊性癌(PCACC)是一种罕见的附件皮肤肿瘤,于1975年首次描述,迄今为止,仅对62例病例进行了详细研究并在英语文献中进行了报道。 PCACC通常被认为是起源/分化中的高教分泌,但其确切的组织发生机制仍不为人所知。在大多数情况下,PCACC的病程相当缓慢,但可引起局部复发,并且很少发生区域(淋巴结)和远处(肺)转移。我们在此报告了一名希腊妇女,该妇女长期存在PCACC,并在数年内缓慢生长,并在区域淋巴结转移,这突显了该肿瘤的潜在侵袭性过程。对原发性和转移性肿瘤进行了免疫组织化学研究,证明它们表达了几种(与汗腺相关的)抗原(例如角蛋白7,上皮膜抗原,CD10和CD117),但既没有激素受体也没有p63或大囊性囊肿性疾病流体蛋白15。回顾了这种罕见的皮肤附件肿瘤的主要临床病理特征。

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