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具有XY染色体组成的表型女性的性腺发育不全。

Gonadal dysgenesis in a phenotypic female with an XY chromosomal constitution.

作者信息

Kaplan E

出版信息

S Afr Med J. 1978 Apr 8;53(14):552-3.

PMID:675413
Abstract

A phenotypic female with an XY karyotype and pure gonadal dysgenesis is described. Bilateral streak gonads may be found in patients with features of Turner's syndrome and also in phenotypic females without the somatic abnormalities described in Turner's syndrome. Mixed gonadal dysgenesis refers to the presence of a unilateral streak gonad and contralateral testis in a phenotypic female. Dysgenetic gonads are more liable to undergo malignant change, especially in patients with an XY karyotype, and in those with mixed gonadal dysgenesis. Laparotomy and removal of the dysgenetic gonads is indicated in patients with an XY karyotype. If a 46,XX chromosomal pattern is present, the malignant potential is probably less, but laparotomy is still indicated to enable a prognosis to be given regarding fertility.

摘要

本文描述了一名具有XY核型和单纯性腺发育不全的表型女性。双侧条索状性腺可见于具有特纳综合征特征的患者,也可见于无特纳综合征所描述的躯体异常的表型女性。混合性性腺发育不全是指表型女性中存在单侧条索状性腺和对侧睾丸。发育异常的性腺更容易发生恶变,尤其是XY核型的患者以及混合性性腺发育不全的患者。对于XY核型的患者,建议行剖腹术并切除发育异常的性腺。如果存在46,XX染色体模式,恶变可能性可能较小,但仍建议行剖腹术以判断生育预后。

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