Takano M, Yamashita S, Inuzuka S, Suzu H
Division of Urology, Ohmura Municipal Hospital.
Hinyokika Kiyo. 1995 Aug;41(8):613-6.
Here is presented a surprisingly rare case in a 40-year-old male who had patent vitelline duct by nature. However, his congenital disease appeared deceptively to be an acquired umbilical urachal sinus on the diagnostic evaluations including fistulography before surgery. The diagnosis was definitely confirmed after the successful surgical procedure. The principal reason why these diseases were indistinguishable was reviewed. The incidence of each disease and incidence of association with umbilical fistula in each disease were discussed. With regard to these incidences, we compared urachal anomalies with vitelline duct anomalies through reference of several literatures. This is the most unique event we have ever clinically experienced.
本文介绍了一例极为罕见的病例,患者为40岁男性,其卵黄管天生通畅。然而,在包括术前瘘管造影在内的诊断评估中,他的先天性疾病看似是后天性脐尿管窦。手术成功后确诊得以明确。回顾了这些疾病难以区分的主要原因。讨论了每种疾病的发病率以及每种疾病与脐瘘的关联发生率。关于这些发生率,我们通过参考多篇文献,对脐尿管异常和卵黄管异常进行了比较。这是我们临床经历过的最独特的病例。