Literature DB >> 6408781

Blind-ending bifid and double ureters.

E Wespes, W De Sy, A J Thiry, C C Schulman.   

Abstract

Bifid and double blind ureters are two rare congenital anomalies of the upper urinary tract. Usually they are incidental findings. Occasionally, they are associated with urinary tract infection, but the symptoms are not specific. The key to diagnosis is a careful urethral cystoscopy and retrograde pyelogram. Asymptomatic patients without urinary tract infection require no treatment. When symptoms or infection are present, excision of the blind branch is required with antireflux reimplantation of the normal ureter if needed.

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Year:  1983        PMID: 6408781     DOI: 10.1016/0090-4295(83)90198-x

Source DB:  PubMed          Journal:  Urology        ISSN: 0090-4295            Impact factor:   2.649


  3 in total

1.  Cranial blind-ending branch of a bifid ureter.

Authors:  H Kiliçarslan; S Ayan; G Gökçe; K Kaya; E Y Gültekin
Journal:  Int Urol Nephrol       Date:  2001       Impact factor: 2.370

2.  Familial occurrence of blind-ending bifid and duplicated ureters.

Authors:  F Aragona; G P Glazel; G Zacchello; B Andreetta
Journal:  Int Urol Nephrol       Date:  1987       Impact factor: 2.370

3.  The blind-ending bifid ureter.

Authors:  X Giannakopoulos; P Chambilomatis; M Thirothoulakis; G Seferiadis
Journal:  Int Urol Nephrol       Date:  1994       Impact factor: 2.370

  3 in total

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