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卵巢无性细胞瘤伴真两性畸形

Dysgerminoma of the ovary associated with true hermaphroditism.

作者信息

Schwartz I S, Cohen C J, Deligdisch L

出版信息

Obstet Gynecol. 1980 Jul;56(1):102-6.

PMID:7383471
Abstract

A dysgerminoma of the left gonad exhibiting malignant features was diagnosed at laparotomy in a 33-year-old virginal phenotypic female who had a normal menstrual history. Pathologic examination of the contralateral (right) gonad revealed an ovotestis. The nonaffected residual portion of the tumor-bearing left gonad exhibited only ovarian stroma. The ovotestis was characterized by a nodule of testicular parenchyma composed of partly hyalinized seminiferous tubules without evident spermatogenesis. The ovotestis was contiguous to normal ovarian elements, including a cystic corpus luteum and primordial follicles. Proliferative endometrium was found lining the small uterus. The findings are indicative of true hermaphroditism. The occurrence of dysgerminoma and other tumors in association with various forms of gonadl dysgenesis is discussed. To the authors' knowledge, this is the first reported case of dysgerminoma occurring in a phenotypic female hermaphrodite.

摘要

一名33岁、表型为处女、月经史正常的女性在剖腹手术中被诊断出左侧性腺有具有恶性特征的无性细胞瘤。对侧(右侧)性腺的病理检查显示为卵睾。携带肿瘤的左侧性腺未受影响的残余部分仅表现为卵巢基质。卵睾的特征是由部分玻璃样变的生精小管组成的睾丸实质结节,无明显精子发生。卵睾与正常卵巢成分相邻,包括一个囊性黄体和原始卵泡。在小子宫内发现增殖期子宫内膜。这些发现提示为真两性畸形。本文讨论了无性细胞瘤和其他肿瘤与各种形式性腺发育不全的关联。据作者所知,这是首例报道的发生在表型女性两性畸形患者中的无性细胞瘤病例。

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