一例睾丸未降、持续性穆勒氏管综合征和横向睾丸异位患者的睾丸肿瘤:病例报告和文献综述

IF 0.5 Q4 UROLOGY & NEPHROLOGY
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引用次数: 0

摘要

一名 20 岁的男性患者身体特征和第二性征正常,但出现右侧睾丸肿胀。影像学检查发现右侧睾丸肿块,诊断为典型精索瘤。在腹股沟睾丸切除术中,发现右侧有一个实性睾丸肿块和两条精索,一条与肿块相连,另一条与类似睾丸的结构相连。检查显示还有其他睾丸和一个不发育的子宫,这表明这是一例罕见的睾丸肿瘤与睾丸下降不全和横向睾丸异位(TTE)并存的病例,患者是一名患有 "持续性穆勒氏管综合征"(PMDS)的假两性人。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Testicular tumor in a case of, undescended testes, persistent mullerian duct syndrome and transverse testicular ectopia: Report of a case and review of the literature

A 20-year-old with normal male body features and secondary sexual characteristics presented with a right testicular swelling. Imaging revealed a right testicular mass, leading to a diagnosis of classical seminoma. During inguinal orchiectomy, a solid testicular mass was found on the right side along with two spermatic cords, one attached to the mass and the other to a structure resembling a testes. Examination showed the presence of other testes and a rudimentary uterus, indicating a rare case of a testicular tumor coexisting with undescended testes and transverse testicular ectopia (TTE) in a Pseudohermaphrodite with “persistent mullerian duct syndrome” (PMDS).

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来源期刊
Urology Case Reports
Urology Case Reports Medicine-Urology
CiteScore
0.90
自引率
20.00%
发文量
325
审稿时长
37 days
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