Key result
Cyclophosphamide-induced cardiotoxicity in a child led to lethal hemorrhagic infarction and coagulative necrosis, suggesting endothelial damage and thrombotic microangiopathy as the pathogenesis.
Why the study?
Does extracorporeal membrane oxygenation improve survival or myocardial recovery in a child with cyclophosphamide-induced cardiotoxicity?
Case Report (n=1)
Does extracorporeal membrane oxygenation improve survival or myocardial recovery in a child with cyclophosphamide-induced cardiotoxicity?
Answers are grounded in this paper and cite their sources.
This case highlights that cyclophosphamide-induced cardiotoxicity involves severe endothelial damage and thrombotic microangiopathy, which may remain lethal despite mechanical circulatory support with ECMO.
We present a clinicopathologic study of the youngest reported child with lethal cyclophosphamide-induced cardiotoxicity after hematopoietic stem cell transplantation for β-thalassemia major and the 1st pediatric report of the use of extracorporeal membrane oxygenation as a therapeutic modality to bridge the patient to myocardial recovery. Despite improvement in myocardial function while on extracorporeal membrane oxygenation, at autopsy 11 days after the onset of cardiac dysfunction, epicardial hemorrhage and extensive myocardial hemorrhagic infarction were revealed. Histopathologic and ultrastructural examination of the myocardium revealed extensive coagulative necrosis of cardiomyocytes, endothelial damage, fibrin thrombi, and subendothelial and interstitial fibrin. We review the literature on cyclophosphamide-induced cardiotoxicity and describe its clinicopathologic characteristics. Our findings point to endothelial damage leading to thrombotic microangiopathy and ischemic tissue injury as the most likely pathogenesis.
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Meserve et al. (2013) conducted a case report in Cyclophosphamide-induced cardiotoxicity after stem cell transplantation for β-thalassemia major (n=1). Extracorporeal membrane oxygenation was evaluated. Cyclophosphamide-induced cardiotoxicity in a child led to lethal hemorrhagic infarction and coagulative necrosis, suggesting endothelial damage and thrombotic microangiopathy as the pathogenesis.
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