Bladder necrosis presenting with hematuria in a patient with sickle-cell disease
Abstract
We present an interesting case of bladder necrosis in an 11-year-old boy with sickle-cell disease. The patient initially presented with sudden onset of abdominal pain and went on to have gross hematuria with clots and severe dysuria. Cysto-urethroscopy revealed global hemorrhagic cystitis and a suprapubic catheter was inserted percutaneously during cystoscopy. The symptoms spontaneously resolved over several weeks and the child voids normally at last follow-up. Multiple bladder biopsies were taken and all were completely necrotic.
Keywords: Bladder necrosis, Hematuria, Sickle-cell disease, Genitourinary system
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PII: S1477-5131(04)00004-X
doi:10.1016/j.jpurol.2004.11.002
© 2005 Journal of Pediatric Urology Company. Published by Elsevier Inc. All rights reserved.
