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真两性畸形,双侧卵睾、双侧性腺母细胞瘤和无性细胞瘤,核型为46,XX/46,XY,且成功妊娠。

True hermaphrodite with bilateral ovotestes, bilateral gonadoblastomas and dysgerminomas, 46,XX/46,XY karyotype, and a successful pregnancy.

作者信息

Talerman A, Verp M S, Senekjian E, Gilewski T, Vogelzang N

机构信息

Department of Pathology, University of Chicago, Illinois.

出版信息

Cancer. 1990 Dec 15;66(12):2668-72. doi: 10.1002/1097-0142(19901215)66:12<2668::aid-cncr2820661234>3.0.co;2-5.

Abstract

The first case (to the authors' knowledge) is reported of a true hermaphrodite with bilateral ovotestes, bilateral gonadoblastomas and dysgerminomas, a 46, XX/46,XY karyotype, and a successful pregnancy. The true hermaphroditism was diagnosed during infancy. The patient was subsequently found to have a gonadoblastoma and a microscopic dysgerminoma in the gonad diagnosed as an ovotestis and excised during infancy. The successful pregnancy occurred when the patient was 29 years old. A year later a large gonadal tumor affecting the remaining gonad was excised. The gonad was found to be an ovotestis, and the tumor was a dysgerminoma arising from a gonadoblastoma. This case further emphasizes the malignant potential of the Y chromosome in patients with abnormal gonads.

摘要

据作者所知,首例双侧卵睾、双侧性腺母细胞瘤和无性细胞瘤并存的真两性畸形患者被报道,其核型为46,XX/46,XY,并成功妊娠。该真两性畸形在婴儿期被诊断。随后发现该患者在婴儿期被诊断为卵睾并切除的性腺中有一个性腺母细胞瘤和一个显微镜下可见的无性细胞瘤。患者29岁时成功妊娠。一年后,切除了影响剩余性腺的一个大的性腺肿瘤。发现该性腺为卵睾,肿瘤是起源于性腺母细胞瘤的无性细胞瘤。该病例进一步强调了性腺异常患者中Y染色体的恶性潜能。

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