Open Access
CASE REPORT
Stuttering priapism associated with hereditary spherocytosis
Kartik Prabhakaran, Bruce L. Jacobs, Marc C. Smaldone, Michael E. Franks
Department of Urology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA
Address correspondence to Dr. Bruce L. Jacobs, Department
of Urology, University of Pittsburgh School of Medicine,
3471 5th Avenue, Suite 700, Pittsburgh, PA 15213-3232 USA
Canadian Journal of Urology 2007, 14(5), 3702-3704.
Abstract
Stuttering priapism is a clinical phenomenon that occurs
commonly in certain patient populations, including
sickle cell anemia and other hematologic dyscrasias.
Although the mechanism is still not completely
understood, treatment is focused on prevention of
recurrence in the outpatient setting, and immediate
detumescence and minimizing corporal fibrosis in the
acute setting. We present a case of stuttering priapism
in a 44 year-old male with hereditary spherocytosis and
discuss the pathophysiology and clinical management
of this entity.
Keywords
priapism, spherocytosis, stuttering
Cite This Article
APA Style
Prabhakaran, K., Jacobs, B.L., Smaldone, M.C., Franks, M.E. (2007). Stuttering priapism associated with hereditary spherocytosis. Canadian Journal of Urology, 14(5), 3702–3704.
Vancouver Style
Prabhakaran K, Jacobs BL, Smaldone MC, Franks ME. Stuttering priapism associated with hereditary spherocytosis. Can J Urology. 2007;14(5):3702–3704.
IEEE Style
K. Prabhakaran, B.L. Jacobs, M.C. Smaldone, and M.E. Franks, “Stuttering priapism associated with hereditary spherocytosis,” Can. J. Urology, vol. 14, no. 5, pp. 3702–3704, 2007.
Copyright © 2007 The Canadian Journal of Urology.