首页> 美国卫生研究院文献>Case Reports in Urology >Gubernaculum Sparing Laparoscopic Orchiopexy in Cryptorchidism with Ipsilateral Congenital Absence of the Vas Deferens: Unique Outcome
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Gubernaculum Sparing Laparoscopic Orchiopexy in Cryptorchidism with Ipsilateral Congenital Absence of the Vas Deferens: Unique Outcome

机译:Gubernaculum保留腹腔镜睾丸检查在隐睾症与同侧先天性输精管缺如:独特的结果

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摘要

Congenital absence of the vas deferens (CAVD) is an uncommon anomaly that occurs in up to 1% of the male population. It can be associated with various other anomalies, including cryptorchidism and renal anomalies, such as renal agenesis. We here present a case of cryptorchidism with ipsilateral congenital absence of the vas deferens and renal agenesis and used the Stephen-Fowler technique for Orchiopexy depending on gubernacular vessels. A 7-month-old boy was referred to our center with left grade 2 hydronephrosis, right renal agenesis, and right impalpable, undescended testis. Examination under anesthesia and laparoscopic exploration with staged Stephen-Fowler orchiopexy were performed. The patient was followed up at 3, 6, and 12 months and had an excellent outcome. Cryptorchidism with congenital ipsilateral absence of the vas deferens and renal agenesis is a rare diagnostic entity. Our case supports the suggested theory that the gubernacular vessels can increase the blood supply to the testis, although further studies are needed to confirm this hypothesis.
机译:先天性输精管缺乏症(CAVD)是一种罕见的异常现象,发生在多达1%的男性人群中。它可能与其他各种异常有关,包括隐睾症和肾脏异常,例如肾脏发育不全。我们在这里介绍了一个伴有同侧先天性输精管和肾发育不全的隐睾症的病例,并根据斯蒂芬-福勒技术对睾丸视性使用了视管。一名7个月大的男孩因左2级肾积水,右肾发育不全和右无法触及的睾丸下降而被转介到我们中心。进行了麻醉检查和分期进行的Stephen-Fowler睾丸手术的腹腔镜探查。对该患者进行了3、6和12个月的随访,结果良好。先天性同侧无输精管和肾脏发育不全的隐睾是一种罕见的诊断实体。我们的案例支持建议的理论,即鼻烟管可以增加向睾丸的血液供应,尽管还需要进一步的研究来证实这一假说。

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