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三名核型为46,XY的两性畸形患者中的生殖细胞肿瘤。

Germ cell neoplasms in three intersex patients with 46,XY karyotype.

作者信息

Petersen L, Kock K, Jacobsen B B

机构信息

Department of Urology, Odense University Hospital, Denmark.

出版信息

Int Urol Nephrol. 1992;24(6):633-9. doi: 10.1007/BF02551299.

Abstract

This report presents 3 cases with gonadoblastoma mixed with other germ cell tumours in intersex patients, all with a 46,XY karyotype. One 11-year-old patient was a true hermaphrodite, the others, aged 13 and 18, respectively, had both gonadal dysgenesis. Different clinical courses have been noted. Two patients had gonadoblastoma combined with dysgerminoma; in one of them a teratoma was also found. In the third case gonadoblastoma was transformed into teratocarcinoma. The malignant degeneration was more serious in the 2 pubertal patients. Thus, we recommend early and prophylactic gonadectomy.

摘要

本报告介绍了3例两性畸形患者中混合有其他生殖细胞肿瘤的性腺母细胞瘤病例,所有患者核型均为46,XY。1例11岁患者为真两性畸形,另外2例分别为13岁和18岁,均患有性腺发育不全。观察到不同的临床病程。2例患者性腺母细胞瘤合并无性细胞瘤,其中1例还发现了畸胎瘤。第3例性腺母细胞瘤转变为畸胎癌。青春期患者的恶性变更为严重。因此,我们建议早期进行预防性性腺切除术。

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