Lüscher K P, Hanimann B, Morger R
Frauenklinik Kantonsspital Münsterlingen.
Zentralbl Gynakol. 1987;109(18):1111-7.
When double uterus is observed, absence of one kidney is common. These rare congenital anomalies are known in literature. In the years 1980-1984 we observed four cases. Symptoms, diagnosis and therapy are described. Preoperative diagnosis is now much better by ultrasonography. Nevertheless operative procedure has to be adapted to the real anatomic situation at first within the intervention. In one case a second operation was necessary because of a recurrence. This case is described in detail.
当发现双子宫时，一侧肾脏缺如很常见。这些罕见的先天性异常在文献中已有记载。在1980年至1984年期间，我们观察到4例。本文描述了其症状、诊断和治疗方法。目前，通过超声检查术前诊断有了很大改善。然而，手术操作首先必须根据术中实际解剖情况进行调整。有1例因复发需要再次手术。本文对此病例进行了详细描述。
