论文部分内容阅读
家族性精索扭转临床罕见。在以往的英文文献中仅有四篇报告,本文系第五篇。由于意识到家族遗传病史,就诊后几乎没有延误诊治并及时行睾丸救治。病人包括同母异父的三兄弟和一个患病的父亲, 易于鞘膜内精索扭转的解剖异常被认为是鞘膜高位包裹于精索上,延长了睾丸系膜。本文中父亲拒绝手术给予手法复位治愈,3例双侧异常的兄弟(均为16岁),均经手术探查证实解剖异常。Ouningham于1960年报道了第一篇家族性睾丸扭转,文中3个男孩发病年龄分别是(14、15、21
Familial spermatic cord twisting clinical rare. In the past English literature only four reports, this article is the fifth. Due to the awareness of the family history of genetic disease, after treatment almost no delay in diagnosis and treatment of line testicular salvage. Anatomy of an easily sphincterous suture that is anomalous in the sheath is thought to involve the high sheath of the sheath in the spermatic cord, prolonging the testicular mesothelium. In this article, my father refuses surgery to give the hand reduction and cure. Three cases of bilateral abnormalities (all 16 years old) were confirmed by surgical exploration. Ouningham reported the first familial testicular torsion in 1960, in which the age at onset of three boys was (14, 15, 21