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Article
October 1975

Pancytopenia in a Patient With Sickle Cell Anemia

Author Affiliations

From the Department of Pediatrics (Drs Kim, Karayalcin, and Aballi) and Division of Hematology (Dr Rosner), Queens Hospital Center, Affiliation of the Long Island Jewish-Hillside Medical Center, Jamaica, NY; and the Health Sciences Center, State University of New York at Stony Brook (Drs Karayalcin, Rosner, and Aballi).

Am J Dis Child. 1975;129(10):1195-1196. doi:10.1001/archpedi.1975.02120470045012
Abstract

• An 11-year-old black boy with sickle cell anemia developed profound pancytopenia during the course of his disease, but fully recovered therefrom. The patient was receiving anticonvulsant drugs for a seizure disorder secondary to a "stroke," and, therefore, a drug-related marrow aplasia cannot be ruled out.

(Am J Dis Child 129:1195-1196, 1975)

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