Thrombotic microangiopathy in patients with sickle cell disease.
Gabriella Biasi CarrascoPatricia Belintani BlumJosefina Aparecida Pellegrini BragaPublished in: Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo (2024)
TMA is a serious, life-threatening disease, characterized by microangiopathic hemolytic anemia, thrombocytopenia, and organ damage. The association of SCD and TMA is difficult to diagnose, since they can share a similar clinical presentation. Recognizing this association and promptly instituting treatment may impact the survival of these patients.