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Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
Splenic infarction due to concomitant hereditary spherocytosis and sickle cell trait
Robin Yates Dulman1, George R Buchanan, Howard Ginsburg
1Department of Pediatric Hematology/Oncology, NYU School of Medicine, New York, NY 10016, USA. yatesr01@med.nyu.edu
Abstract:
Concomitant hereditary spherocytosis and sickle cell trait, although extremely rare, could potentially lead to splenic sequestration or infarction. We report here the first case of splenic infarction in a child with hereditary spherocytosis and sickle cell trait while flying on a commercial aircraft. The presence of hypoxia, hemoconcentrated erythrocytes, and sickle hemoglobin created the perfect environment for clinical sequelae.
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