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一名具有特纳综合征特征的46,XY女性患者的青春期前性腺母细胞瘤。

Prepubertal gonadoblastoma in a 46,XY female patient with features of Turner syndrome.

作者信息

Alikaşifoğlu A, Kandemir N, Cağlar M, Kotiloğlu E, Yordam N

机构信息

Hacettepe University, Division of Paediatric Endocrinology, Ankara, Turkey.

出版信息

Eur J Pediatr. 1996 Aug;155(8):653-5. doi: 10.1007/BF01957146.

Abstract

UNLABELLED

46,XY gonadal dysgenesis was diagnosed in a 5.5-year-old phenotypically female patient who had physical and somatic stigmata of Turner syndrome such as webbed neck, low hairline, widely spaced nipples, cubitus valgus and coarctation of the aorta. Bilateral streak gonads were removed and an unsuspected gonadoblastoma was found in right gonad.

CONCLUSION

The prepubertal development of gonadal neoplasm in patient with Xy gonadal dysgenesis indicated the necessity of gonadectomy at the time of diagnosis.

摘要

未标注

一名5.5岁表型为女性的患者被诊断为46,XY性腺发育不全,其具有特纳综合征的身体和躯体特征,如蹼颈、低发际线、乳头间距宽、肘外翻和主动脉缩窄。双侧条索状性腺被切除,右侧性腺中发现了意外的性腺母细胞瘤。

结论

XY性腺发育不全患者性腺肿瘤的青春期前发育表明在诊断时进行性腺切除术的必要性。

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