Rare Cause of Restrictive Cardiomyopathy: A Case Report of Löffler Endocarditis.

IF 0.5 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
Case Reports in Cardiology Pub Date : 2026-08-17 eCollection Date: 2026-01-01 DOI:10.1155/cric/5307648
Jose L Diz Ferre, Edward G Soltesz, Agostina Fava
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引用次数: 0

Abstract

Löffler endocarditis, an idiopathic hypereosinophilic syndrome, can present symptoms of heart failure and peripheral eosinophilia. We present the case of a 46-year-old woman with fatigue, shortness of breath, and edema, who was found to have thrombocytopenia, elevated cardiac biomarkers, and hypereosinophilia (2.96 k/uL). Cardiac MRI revealed hypertrophic cardiomyopathy, right ventricular hypertrophy, and a restrictive filling pattern, raising suspicion for Löffler endocarditis. Despite initial corticosteroid and diuretic treatment, she was readmitted with persistent symptoms. This case highlights the diagnostic imaging and treatment challenges with corticosteroid therapy, to control eosinophilic infiltration and prevent irreversible cardiac damage. Löffler endocarditis should be considered in the imaging differential diagnosis of unexplained heart failure.

限制性心肌病的罕见病因:Löffler心内膜炎1例报告。
Löffler心内膜炎是一种特发性嗜酸性细胞增多综合征,可表现为心力衰竭和周围嗜酸性细胞增多症。我们报告一例46岁的女性患者,她有疲劳、呼吸短促和水肿,被发现有血小板减少症、心脏生物标志物升高和嗜酸性粒细胞增多症(2.96 k/uL)。心脏MRI显示肥厚性心肌病,右心室肥厚和限制性充盈模式,引起Löffler心内膜炎的怀疑。尽管最初接受了皮质类固醇和利尿剂治疗,但她仍因持续症状再次入院。本病例强调了皮质类固醇治疗的诊断、影像学和治疗挑战,以控制嗜酸性粒细胞浸润和防止不可逆的心脏损伤。Löffler心内膜炎应考虑在影像学鉴别诊断不明原因的心力衰竭。
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来源期刊
Case Reports in Cardiology
Case Reports in Cardiology CARDIAC & CARDIOVASCULAR SYSTEMS-
自引率
0.00%
发文量
63
审稿时长
13 weeks
期刊介绍: Case Reports in Cardiology is a peer-reviewed, Open Access journal that publishes case reports and case series related to hypertension, arrhythmia, congestive heart failure, valvular heart disease, vascular disease, congenital heart disease and cardiomyopathy.
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