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颗粒细胞瘤:病理学与组织发生学综述

Granular cell tumor: a review of the pathology and histogenesis.

作者信息

Ordóñez N G, Mackay B

机构信息

The University of Texas, M.D. Anderson Cancer Center, Houston 77030, USA.

出版信息

Ultrastruct Pathol. 1999 Jul-Aug;23(4):207-22. doi: 10.1080/019131299281545.

Abstract

As the name suggests, the histogenesis of the granular cell tumor is uncertain, but this intriguing neoplasm has occasioned much speculation and controversy since its description in 1926 as a myoblastoma. Though ubiquitous in its anatomic location, it is usually small, solitary, benign, and readily recognized by routine light microscopy, and questions concerning it are principally academic. However, a small number of cases are malignant and they can be difficult to identify in paraffin sections. The combined input from immunohistochemistry and electron microscopy has greatly clarified understanding of the morphology of this lesion and both methods are helpful when the differential diagnosis is a problem. The cell of origin is still undecided, and although distinct neural features argue for Schwannian origin, the noncommittal term granular cell tumor continues to be appropriate.

摘要

顾名思义,颗粒细胞瘤的组织发生尚不确定,但自1926年被描述为成肌细胞瘤以来,这种引人入胜的肿瘤引发了诸多猜测和争议。尽管其解剖位置广泛,但通常体积较小、孤立、良性,通过常规光学显微镜很容易识别,关于它的问题主要是学术性的。然而,少数病例是恶性的,在石蜡切片中可能难以识别。免疫组织化学和电子显微镜的联合应用极大地澄清了对该病变形态的认识,当鉴别诊断出现问题时,这两种方法都很有帮助。细胞起源仍未确定,尽管明显的神经特征支持雪旺氏起源,但“颗粒细胞瘤”这个不明确的术语仍然适用。

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