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膀胱不完全重复伴多发先天性畸形:一种罕见表现。

Incomplete bladder duplication with multiple congenital anomalies: A rare presentation.

作者信息

Awasthi Nipun Kumar, Goel Hemantkumar, Mahapatra Rajkumarsingha, Pal Dilipkumar

机构信息

Department of Urology, I. P. G. M. E. & R., Kolkata, West Bengal, India.

出版信息

Urol Ann. 2015 Jan-Mar;7(1):88-90. doi: 10.4103/0974-7796.148628.

Abstract

We report a rare case of incomplete bladder duplication associated with multiple congenital malformation. The patient presented with a symptomatic left pelvi-ureteric junction obstruction which was surgically managed. To the best of our knowledge, this type of bladder duplication with such syndromic association is not yet reported in literature.

摘要

我们报告了一例罕见的伴有多种先天性畸形的不完全膀胱重复病例。患者因有症状的左侧肾盂输尿管连接处梗阻就诊,并接受了手术治疗。据我们所知,这种伴有综合征关联的膀胱重复类型在文献中尚未见报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f84d/4310127/bde14e326f1b/UA-7-88-g001.jpg

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