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45,X条索状性腺综合征伴双侧“萎缩型”性腺母细胞瘤。

45,X streak gonad syndrome associated with bilateral 'burnt out' gonadoblastoma.

作者信息

Bösze P, Magyar E, Tóth A, László J

机构信息

Department of Obstetrics and Gynecology, Postgraduate Medical University, Budapest, Hungary.

出版信息

Gynecol Obstet Invest. 1989;28(3):113-7. doi: 10.1159/000293544.

Abstract

A 28-year-old woman with well-developed female secondary sexual characteristics, secondary amenorrhea, short stature and a few somatic anomalies of streak gonad syndrome who had bilateral 'burnt out' gonadoblastoma associated with 45,X karyotype is reported. Although the exact source of steroid production in the present case could not be defined, it seems probable that the tumor once secreted steroid hormones which were responsible for the development of the female secondary sexual characteristics. At the time of diagnosis there was no evidence of hormonal activity of the tumor. Cases of gonadoblastoma without Y chromosome are reviewed. The diagnostic difficulties encountered in patients with gonadoblastoma not associated with Y chromosome are discussed.

摘要

报告了一名28岁女性,其具有发育良好的女性第二性征、继发性闭经、身材矮小以及条索状性腺综合征的一些躯体异常,患有双侧“消退型”性腺母细胞瘤,核型为45,X。尽管本病例中类固醇产生的确切来源无法确定,但肿瘤似乎曾经分泌过负责女性第二性征发育的类固醇激素。诊断时,没有肿瘤激素活性的证据。对无Y染色体的性腺母细胞瘤病例进行了综述。讨论了与Y染色体无关的性腺母细胞瘤患者所遇到的诊断困难。

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