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Published on: October 14, 2009
Late-Stage Löffler's Endocarditis Mimicking Cardiac Tumor: A Case Report
Takafumi Koyama1, Hiroyuki Yamamoto2, Manabu Matsumoto3
1Department of Cardiology, Shonan Fujisawa Tokushukai Hospital, Kanagawa, Japan.
Insights
Löffler's endocarditis, a rare heart condition linked to hypereosinophilic syndrome, can mimic cardiac tumors. Early diagnosis and treatment with anticoagulation and corticosteroids are crucial for favorable outcomes.
Area of Science:
- Cardiology
- Hematology
- Pathology
Background:
- Hypereosinophilic syndrome (HES) is a rare disorder characterized by persistent eosinophilia.
- Cardiac involvement in HES, known as Löffler's endocarditis, is a serious complication.
- Löffler's endocarditis can present insidiously or dramatically, often mimicking other cardiac pathologies.
Observation:
- A case of HES presented with a cardiac mass and abnormal electrocardiogram, initially suspected as a malignant cardiac tumor.
- Multimodality imaging suggested a tumor invading the papillary muscle, necessitating surgical intervention.
- Surgical pathology revealed thrombosis and myocardial damage due to eosinophilic infiltration, not malignancy.
Findings:
- The final diagnosis was late-stage Löffler's endocarditis, confirmed by pathological examination.
- Surgical resection of the cardiac mass and endomyocardial resection with mitral valve replacement were successfully performed.
- A combination of anticoagulation and corticosteroids proved effective in managing the condition.
Implications:
- This case underscores the diagnostic challenges posed by cardiac masses in HES.
- It highlights potential pitfalls in interpreting cardiac imaging for thrombus versus tumor.
- Considering Löffler's endocarditis in the differential diagnosis of cardiac masses is clinically significant for timely and appropriate management.
Abstract:
Löffler's endocarditis (cardiac involvement in hypereosinophilic syndrome) is rare yet life-threatening if left untreated. We describe a case of hypereosinophilic syndrome presenting as a cardiac mass with an abnormal electrocardiogram. Diagnostic studies of the cardiac mass strongly suggested a malignant cardiac tumor invading the papillary muscle. Thus, excision of the cardiac mass and endomyocardial resection with mitral valve replacement were successfully performed. Pathology revealed various stages of thrombosis and irreversible myocardial damage caused by eosinophilic infiltration with no malignancy, leading to the correct diagnosis of late-stage Löffler's endocarditis. The subsequent combination of anticoagulation and corticosteroids was effective with a favorable outcome. This case highlights pitfalls in multimodality imaging of cardiac thrombus and the clinical significance of considering Löffler's endocarditis in the diagnostic work-up of a cardiac mass.
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