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卵巢支持-间质细胞瘤。一项临床、病理及超微结构研究,特别涉及这些肿瘤的组织发生。

Ovarian Sertoli-Leydig cell tumors. A clinical, pathological and ultrastructural study with particular reference to the histogenesis of these tumors.

作者信息

Genton C Y

出版信息

Arch Gynecol. 1980;230(1):49-75. doi: 10.1007/BF02108598.

Abstract

Ovarian Sertoli-Leydig cell tumors are rare, most of them being endocrinologically active and causing virilization. Their histogenesis and nomenclature are still under discussion. Six such tumors were identified in the Laboratory for Histopathology of the University Women's Hospital, Zürich. The clinical data as well as the macroscopic, microscopic and ultrastructural features of these tumors are analysed and discussed. In an attempt to clarify their histogenesis, the ultrastructural features of these tumors have been compared with those of two granulosa cell tumors as well as with those of a testis in a patient with testicular feminization. Our own results and a study of published data suggest that Sertoli-Leydig cell tumors arise from ovarian stroma. Because of their obvious morphological similarities to testicular structures they should be termed "gonadal stromal tumors of android type".

摘要

卵巢支持-间质细胞瘤罕见,其中大多数具有内分泌活性并导致男性化。其组织发生和命名仍在讨论中。苏黎世大学妇女医院组织病理学实验室鉴定出6例此类肿瘤。对这些肿瘤的临床资料以及大体、显微镜和超微结构特征进行了分析和讨论。为了阐明其组织发生,将这些肿瘤的超微结构特征与2例颗粒细胞瘤以及1例睾丸女性化患者的睾丸超微结构特征进行了比较。我们自己的结果以及对已发表数据的研究表明,支持-间质细胞瘤起源于卵巢间质。由于它们与睾丸结构明显的形态学相似性,应将其称为“男性化型性腺间质肿瘤”。

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