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45,X特纳综合征中的无性细胞瘤:一例报告。

Dysgerminoma in 45,X Turner syndrome: report of a case.

作者信息

Sinisi A A, Perrone L, Quarto C, Barone M, Bellastella A, Faggiano M

机构信息

Istituto di Endocrinologia, I Facoltà di Medicina, Università di Napoli, Italy.

出版信息

Clin Endocrinol (Oxf). 1988 Feb;28(2):187-93. doi: 10.1111/j.1365-2265.1988.tb03655.x.

Abstract

Here we report the fourth case of dysgerminoma in a patient with the syndrome of gonadal dysgenesis and 45,X karyotype. Typical Turner's syndrome features were unusually associated with breast development, menarche and secondary amenorrhoea. Exaggerated basal and GnRH stimulated gonadotrophin and low oestradiol levels were typical of post-pubertal Turner's syndrome. Detailed (standard) chromosome and banding analysis excluded the presence of Y chromosome material. This case suggests that the presence of a Y chromosome is not necessary for abnormal differentiation of germ cells and the occurrence of a gonadoblastoma.

摘要

在此,我们报告第四例患有性腺发育不全综合征及45,X核型的患者发生无性细胞瘤的病例。典型的特纳综合征特征异常地与乳房发育、初潮和继发性闭经相关。基础促性腺激素和GnRH刺激后的促性腺激素水平升高以及雌二醇水平降低是青春期后特纳综合征的典型表现。详细的(标准)染色体和显带分析排除了Y染色体物质的存在。该病例表明,Y染色体的存在并非生殖细胞异常分化和性腺母细胞瘤发生的必要条件。

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