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Gubernaculum Sparing Laparoscopic Orchiopexy in Cryptorchidism with Ipsilateral Congenital Absence of the Vas Deferens: Unique Outcome

机译:普别纳庭在Chedptorchidism中备受腹腔镜占毒蕈族患者的同侧先天性缺席,导热剂: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:先天性缺乏输精管(CAVD)是一种罕见的异常,其出现高达1%的男性人群。它可以与各种其他异常相关联,包括密码刺激性和肾异常,例如肾功能衰退。我们在这里提出了一种伴随着激艇的案例,患有输精管和肾功能衰退的同侧先天性缺失,并根据植物血管使用蛇粪锻造渣油技术。一个7个月大的男孩被引用到我们的中心,左2级肾盂鼻病,右肾功能亢进,右易动,睾丸。进行了麻醉和腹腔镜勘探与斯蒂芬 - 福勒占毒蛇病的腹腔镜勘探。患者随访3,6和12个月,结果出色。对先天性同侧没有输精管和肾功能衰退的密码刺激性是一种罕见的诊断实体。我们的案例支持建议的理论,即孕膜血管可以增加睾丸的血液供应,尽管需要进一步研究来证实这一假设。

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