睾丸横向异位伴完全下降至对侧阴囊底部1例。

Q4 Medicine
Shinya Abe, Kazuma Hiramatsu, Toshihide Hosomi, Takashi Matsuoka, Yuki Kamiyama, Naofumi Tsutsumi, Takehiko Segawa
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引用次数: 0

摘要

我们报告一例睾丸横向异位(TTE)完全下降到对侧阴囊。一位55岁的男性左腹股沟恶性淋巴瘤患者通过CT扫描被诊断为TTE和持续性勒管综合征(PMDS)。超声及触诊未见睾丸恶性病变。考虑到勒氏管残余恶性转化的罕见性,我们选择通过触诊和超声随访。TTE通常在儿童时期被诊断出来,因此成人病例相对较少。由于睾丸完全下降,这种情况特别值得注意。我们还收集了1980年以来日本成人TTE病例的数据。在此,我们提出这个病例的TTE以及文献综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[A Case of Transverse Testicular Ectopia with Complete Descent to the Bottom of the Contralateral Scrotum].

We report a case of transverse testicular ectopia (TTE) with complete descent to the contralateral scrotum. A fifty-five-year-old man with malignant lymphoma in the left inguinal region was diagnosed with TTE and persistent Müllerian duct syndrome (PMDS) via CT scan. Ultrasound imaging and palpation revealed no malignant findings in the testes. Given the rarity of malignant transformation in müllerian duct remnant, we opted for follow-up through palpation and ultrasound. TTE is typically diagnosed in childhood, making adult cases comparatively rare. This case is particularly notable due to the complete descent of the testes. We also collected data on Japanese adult cases of TTE since 1980. Herein, we present this case of TTE along with a review of the literature.

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来源期刊
Acta Urologica Japonica
Acta Urologica Japonica Medicine-Medicine (all)
CiteScore
0.20
自引率
0.00%
发文量
74
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