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汗腺和皮脂腺肿瘤的组织病理学专题

Topics in histopathology of sweat gland and sebaceous neoplasms.

作者信息

Ansai Shin-Ichi

机构信息

Division of Dermatology and Dermatopathology, Nippon Medical School Musashi Kosugi Hospital, Kawasaki City, Japan.

出版信息

J Dermatol. 2017 Mar;44(3):315-326. doi: 10.1111/1346-8138.13555.

Abstract

This article reviews several topics regarding sweat gland and sebaceous neoplasms. First, the clinicopathological characteristics of poroid neoplasms are summarized. It was recently reported that one-fourth of poroid neoplasms are composite tumors and one-fourth are apocrine type lesions. Recent progress in the immunohistochemical diagnosis of sweat gland neoplasms is also reviewed. CD117 can help to distinguish sweat gland or sebaceous tumors from other non-Merkel cell epithelial tumors of the skin. For immunohistochemical differential diagnosis between sweat gland carcinoma (SGC) other than primary cutanesous apocrine carcinoma and skin metastasis of breast carcinoma (SMBC), a panel of antibodies may be useful, including p63 (SGC , SMBC ), CK5/6 (SGC , SMBC ), podoplanin (SGC , SMBC ) and mammaglobin (SGC , SMBC ). Comparison of antibodies used for immunohistochemical diagnosis of sebaceous carcinoma (SC) suggests that adipophilin has the highest sensitivity and specificity. Some authors have found that immunostaining for survivin, androgen receptor and ZEB2/SIP1 has prognostic value for ocular SC, but not extraocular SC. In situ SC is rare, especially extraocular SC, but there have been several recent reports that actinic keratosis and Bowen's disease are the source of invasive SC. Finally, based on recent reports, classification of sebaceous neoplasms into three categories is proposed, which are sebaceoma (a benign neoplasm with well-defined architecture and no atypia), borderline sebaceous neoplasm (low-grade SC; an intermediate tumor with well-defined architecture and nuclear atypia) and SC (a malignant tumor with invasive growth and evident nuclear atypia).

摘要

本文综述了有关汗腺和皮脂腺肿瘤的几个主题。首先,总结了类汗孔瘤的临床病理特征。最近有报道称,四分之一的类汗孔瘤为复合性肿瘤,四分之一为大汗腺型病变。还综述了汗腺肿瘤免疫组化诊断的最新进展。CD117有助于将汗腺或皮脂腺肿瘤与其他非默克尔细胞皮肤上皮肿瘤区分开来。对于原发性皮肤大汗腺癌以外的汗腺癌(SGC)与乳腺癌皮肤转移(SMBC)的免疫组化鉴别诊断,一组抗体可能有用,包括p63(SGC、SMBC)、CK5/6(SGC、SMBC)、足板蛋白(SGC、SMBC)和乳腺珠蛋白(SGC、SMBC)。用于皮脂腺癌(SC)免疫组化诊断的抗体比较表明,脂联素具有最高的敏感性和特异性。一些作者发现,survivin、雄激素受体和ZEB2/SIP1的免疫染色对眼部SC有预后价值,但对眼外SC没有。原位SC很少见,尤其是眼外SC,但最近有几份报告称光化性角化病和鲍温病是侵袭性SC的来源。最后,基于最近的报告,提出将皮脂腺肿瘤分为三类,即皮脂腺瘤(一种结构清晰且无异型性的良性肿瘤)、交界性皮脂腺肿瘤(低级别SC;一种结构清晰且有核异型性的中间型肿瘤)和SC(一种具有侵袭性生长和明显核异型性的恶性肿瘤)。

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