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[子宫重复畸形合并单侧肾缺如:5例报告]

[Uterus duplication abnormalities with unilateral kidney agenesis, a report on 5 cases].

作者信息

Hanimann B, Lüscher K P, Morger R

出版信息

Z Kinderchir. 1985 Oct;40(5):299-302. doi: 10.1055/s-2008-1059798.

Abstract

Uterus malformation with renal agenesis at the same time are rare but well-known in literature. The leading symptom is dysmenorrhoea, pain in the lower abdomen increasing with each menstruation and a growing tumour in the small pelvis. We consider sonography of the small pelvis as being the optimal diagnostic examination. Once the diagnosis has been made, a laparotomy is indispensable. Further proceedings depend on the intraoperative result, whether a reconstruction and/or a partial removement of the inner female genital organs is possible or necessary. We could successfully treat 5 cases of genital malformation with ipsilateral renal agenesis.

摘要

子宫畸形同时合并肾缺如的情况较为罕见,但在文献中已有记载。主要症状为痛经,下腹部疼痛随每次月经加重,且盆腔内有不断增大的肿物。我们认为盆腔超声检查是最佳的诊断方法。一旦确诊,剖腹手术是必不可少的。后续治疗取决于术中结果,即是否有可能或有必要对女性内生殖器进行重建和/或部分切除。我们成功治疗了5例伴有同侧肾缺如的生殖器畸形病例。

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