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转移性睾丸网腺癌的超微结构

Ultrastructure of metastatic rete testis adenocarcinoma.

作者信息

Mrak R E, Husain M M, Schaefer R F

机构信息

John L. McClellan Memorial Veterans' Hospital, Little Rock, AR 72205.

出版信息

Arch Pathol Lab Med. 1990 Jan;114(1):84-8.

PMID:2294871
Abstract

Adenocarcinoma of the rete testis is a rare tumor. We describe the ultrastructural appearance of a retroperitoneal adenocarcinoma metastatic from the rete testis, and compare this appearance with that of normal human rete testis. Both normal rete epithelium and the tumor showed deep, narrow nuclear invaginations with apparent nuclear lobulation; small, pleomorphic, electron-dense, membrane-bound granules in the basal cytoplasm; lipid droplets in the apical cytoplasm; and distinctive bulbous cytoplasmic projections along the apical surfaces of the cells. In addition, more general features of glandular tissue were seen. Features notable for their absence were mucin granules, microvilli containing filamentous cores, glycocalyx, and glycocalyceal bodies. The ultrastructural appearance was sufficiently distinctive to suggest that, in the proper clinical context, electron microscopy may serve to support a diagnosis of adenocarcinoma of the rete testis.

摘要

睾丸网腺癌是一种罕见的肿瘤。我们描述了一例从睾丸网转移至腹膜后的腺癌的超微结构表现,并将其与正常人类睾丸网的超微结构进行比较。正常睾丸网上皮和肿瘤均显示细胞核有深而窄的内陷,伴有明显的核分叶;基底细胞质中有小的、多形性的、电子致密的、膜结合颗粒;顶端细胞质中有脂滴;细胞顶端表面有独特的球状细胞质突起。此外,还可见到腺组织的一些更普遍特征。值得注意的是,缺乏黏蛋白颗粒、含有丝状核心的微绒毛、糖萼和糖萼小体。其超微结构表现足够独特,提示在适当的临床背景下,电子显微镜检查可能有助于支持睾丸网腺癌的诊断。

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