| Literature DB >> 8447552 |
S Baruchel1, J Rees, M L Bernstein, P Goodyer.
Abstract
We report a 16-year-old Tanner IV male with homozygous hemoglobin S who presented with recurrent episodes of priapism unresponsive to standard therapy with hydration, analgesia, and exchange transfusion. He had a complete resolution of his symptoms with hydralazine therapy. We therefore suggest a trial of vasodilator therapy for recurrent sickle cell priapism before attempting surgical therapy.Entities:
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Year: 1993 PMID: 8447552 DOI: 10.1097/00043426-199302000-00017
Source DB: PubMed Journal: Am J Pediatr Hematol Oncol ISSN: 0192-8562