A rare case of compartment syndrome and myonecrosis in a patient with hemoglobin SC disease
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Updated: Oct 22, 2025

Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
Muntadhar Al Moosawi1, Hatoon Ezzat2
1Department of Pathology and Laboratory Medicine University of British Columbia Vancouver BC Canada.
Abstract:
Myonecrosis and compartment syndrome are rarely seen in sickle cell disease (SCD), and they have not been previously reported in HbSC disease. This case can potentially be recognized as the first case of a patient with HbSC presenting with spontaneous myonecrosis and compartment syndrome.
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