Severe transplant-associated thrombotic microangiopathy in patients with hemoglobinopathies
Ghada A Abusin1, Rolla Abu-Arja2,3, Rajinder P S Bajwa2,3
1Department of Pediatric Bone Marrow Transplant and Communicable Diseases, University of Michigan, Ann Arbor, Michigan.
Abstract:
Incidence and severity of transplant-associated thrombotic microangiopathy (TA-TMA) in patients with hemoglobinopathies receiving hematopoietic cell transplant is unknown. We report the outcomes for two patients with TA-TMA who received eculizumab. A 2.5-year-old male with sickle cell disease developed TA-TMA-associated pericardial tamponade, severe hypertension, and acute kidney injury 2 months after transplant. A 7-year-old female with β-thalassemia major developed TA-TMA-related acute kidney injury, severe hypertension, and seizures at 6 months after transplant. Both patients progressed to chronic kidney disease (CKD). In patients with hemoglobinopathies, preexisting endothelial dysfunction may place them at a greater risk for TA-TMA and subsequent CKD.
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