Suppr超能文献

[双子宫畸形合并单侧肾缺如]

[Double uterus malformation with unilateral kidney agenesis].

作者信息

Lüscher K P, Hanimann B, Morger R

机构信息

Frauenklinik Kantonsspital Münsterlingen.

出版信息

Zentralbl Gynakol. 1987;109(18):1111-7.

PMID:3687276
Abstract

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.

摘要

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。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验