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默克尔细胞癌:综述

Merkel cell carcinoma: review.

作者信息

Pulitzer Melissa P, Amin Bijal D, Busam Klaus J

机构信息

Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.

出版信息

Adv Anat Pathol. 2009 May;16(3):135-44. doi: 10.1097/PAP.0b013e3181a12f5a.

Abstract

Merkel cell carcinoma (MCC) is synonymous with primary cutaneous neuroendocrine carcinoma. It tends to affects elderly whites, but there is also an increased incidence among immunosuppressed patients. The recent identification of a novel polyomavirus associated with the tumor has stimulated renewed interest in its pathogenesis. MCC tends to show classic histologic features of a neuroendocrine carcinoma and is often positive for CK20, but nonclassic cytologic findings and unusual immunophenotypes may be observed and can lead to a diagnostic confusion. MCC needs to be distinguished from other primary cutaneous tumors with a small cell appearance and metastatic tumors. Surgical excision is the treatment of choice, but radiation therapy has also found to be effective. Sentinel lymph node biopsy has become an integral part of the staging of patients with MCC.

摘要

默克尔细胞癌(MCC)与原发性皮肤神经内分泌癌同义。它倾向于影响老年白人,但免疫抑制患者中的发病率也有所增加。最近发现一种与该肿瘤相关的新型多瘤病毒激发了对其发病机制的新兴趣。MCC往往表现出神经内分泌癌的典型组织学特征,且通常CK20呈阳性,但可能会观察到非典型细胞学表现和不寻常的免疫表型,这可能导致诊断混淆。MCC需要与其他具有小细胞外观的原发性皮肤肿瘤和转移性肿瘤相鉴别。手术切除是首选治疗方法,但放射治疗也已被证明有效。前哨淋巴结活检已成为MCC患者分期的一个组成部分。

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