ArticleJACC. Case reports2026
Loeffler's Endomyocarditis With Embolic Stroke Secondary to Chronic Eosinophilic Leukemia With Therapy-Related Molecular Features.
Article in JACC. Case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
backgroundLoeffler's endomyocarditis is a severe manifestation of hypereosinophilia characterized by eosinophil-mediated myocardial injury, mural thrombus formation, and endomyocardial fibrosis. While often idiopathic, it may arise from clonal eosinophilic disorders carrying higher risk of end-organ damage. CASE SUMMARY: A 77-year-old man with diffuse large B-cell lymphoma in remission presented 5 years after R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone) chemotherapy with subacute confusion and dyspnea. Echocardiography demonstrated a large apical left ventricular thrombus with mildly reduced systolic function. Cardiac magnetic resonance revealed diffuse subendocardial late gadolinium enhancement. Progressive eosinophilia (peak: 3.07 × 10 DISCUSSION: This case highlights clonal, potentially therapy-related eosinophilia as an under-recognized cause of Loeffler's endomyocarditis, requiring early diagnosis to prevent irreversible fibrosis and embolic complications.
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