| Literature DB >> 1086371 |
Abstract
A case of a young man with profound iron deficiency anemia, chronic painless hematuria and urethral bleeding is presented. He had the typical cutaneous findings of Osler-Weber-Rendu disease (hereditary hemorrhagic telangiectasia). Appropriate urological studies demonstrated bladder and urethral telangiectases, with no other explanation for the bleeding. Osler-Weber-Rendu disease should be considered in the differential diagnosis of chronic painless hematuria.Entities:
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Year: 1976 PMID: 1086371 DOI: 10.1016/s0022-5347(17)58969-7
Source DB: PubMed Journal: J Urol ISSN: 0022-5347 Impact factor: 7.450