未被识别的混合性性腺发育不全患者双侧睾丸同步肿瘤：一例报告并文献复习
Bilateral synchronous tumors in testes in unrecognized mixed gonadal dysgenesis: a case report and review of literature.
作者信息
Kulkarni J N, Kamat M R, Borges A M
机构信息
Department of Surgery, Tata Memorial Hospital, Parel, Bombay, India.
出版信息
J Urol. 1990 Feb;143(2):362-4. doi: 10.1016/s0022-5347(17)39964-0.
A case of germ cell tumor occurring simultaneously in the descended and undescended testes of an infertile phenotypic man is reported. Cytogenetic studies revealed a 46XY pattern. Exploration of the abdomen showed a left testicular mass in close proximity to a rudimentary uterus, a fallopian tube and a right testicular mass in the scrotum. Complete excision of both testicular masses and the uterus with the adnexa was done. Histologically, both tumors were seminoma. The patient was well 2 years after treatment.
报道了一例在表型为不育男性的下降和未下降睾丸中同时发生生殖细胞肿瘤的病例。细胞遗传学研究显示为46XY模式。腹部探查发现左侧睾丸肿物紧邻残角子宫、一条输卵管，右侧睾丸肿物位于阴囊内。对双侧睾丸肿物及子宫附件进行了完整切除。组织学检查显示，两个肿瘤均为精原细胞瘤。治疗后2年患者情况良好。
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