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1例伴有Y染色体结构异常(环状Y)的男性假两性畸形

[A case of male pseudohermaphroditism with structural abnormalities of Y chromosome (ring Y)].

作者信息

Watanabe H, Hachisuka Y, Watase H, Fushimi N, Ohtaguro K

机构信息

Department of Urology, Nagoya City University Medical School.

出版信息

Hinyokika Kiyo. 1988 Aug;34(8):1469-74.

PMID:3057830
Abstract

A case of male pseudohermaphroditism with ring Y chromosome is reported. The patient was a 3-year-old boy with hypospadias and right cryptorchidism. Culture of peripheral lymphocytes demonstrated a chromosomal mosaicism of 45 X/46 X, r (Y). Moreover, the chromosomal study with high resolution Q-band method revealed the presence of double ring Y (ring Y and double ring Y with the ratio of 25: 5). A well-developed vagina was discovered by retrograde cystourethrography. Uterus and fallopian tubes were absent at exploratory laparotomy. The gonads existed in the scrotum on the left side and in the inguinal pouch on the right. Both gonads were proved to be testes histologically, but bilateral was deferens were absent and its remnant was found in the retroperitoneal cavity. Plastic surgery for the genital abnormalities was performed. Only 30 cases of ring Y chromosome have been reported in the world including our case and we briefly reviewed these cases.

摘要

本文报道了一例伴有环状Y染色体的男性假两性畸形病例。患者为一名3岁男孩,患有尿道下裂和右侧隐睾。外周血淋巴细胞培养显示染色体嵌合体为45,X/46,X,r(Y)。此外,采用高分辨率Q带法进行染色体研究发现存在双环状Y(环状Y和双环状Y,比例为25:5)。逆行膀胱尿道造影发现有发育良好的阴道。剖腹探查时未发现子宫和输卵管。性腺位于左侧阴囊和右侧腹股沟袋内。组织学检查证实双侧性腺均为睾丸,但双侧输精管缺如,其残余部分位于腹膜后腔。对生殖器异常进行了整形手术。包括我们的病例在内,全世界仅报道了30例环状Y染色体病例,我们对这些病例进行了简要回顾。

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