Correlation Engine 2.0
Clear Search sequence regions


Sizes of these terms reflect their relevance to your search.

A 10-year-old boy with sickle cell disease (SCD) type SC presented with fever and abdominal pain after travel to Ghana and was diagnosed with Plasmodium falciparum infection. Despite adequate antimalarial treatment, he developed evidence of hyperinflammation with marked elevated ferritin, C-reactive protein, and triglycerides and subsequent bone marrow necrosis, characterized by elevated nucleated red blood cells and significant bone pain. This case report highlights the possible association between malaria and bone marrow necrosis in patients with SCD. Important considerations in treatment and workup of patients presenting with malaria and hyperinflammation are discussed.

Citation

Caitlyn Hui, Alessandra Bosch, Oscar Mwizerwa, Jeanine McColl, Antoine Corbeil, Caroline Malcolmson, Deborah M Levy, Zia Bismilla, Shaun K Morris. Case Report: A Case of Bone Marrow Necrosis and Hyperinflammation in a 10-Year-Old Boy after Plasmodium falciparum Infection. The American journal of tropical medicine and hygiene. 2023 Sep 06;109(3):611-615

Expand section icon Mesh Tags


PMID: 37487563

View Full Text