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American Journal of Medical Case Reports. 2021, 9(4), 241-248
DOI: 10.12691/AJMCR-9-4-10
Case Study

Hypereosinophilia and Löffler’s Endocarditis: A Systematic Review

Pramod Theetha Kariyanna1, Naseem A. Hossain2, Neema Jayachamarajapura Onkaramurthy3, Apoorva Jayarangaiah4, Nimrah A. Hossain2, Amog Jayarangaiah5 and Isabel M. McFarlane2,

1Division of Interventional Cardiology, Mount Sinai Heart, Icahn School of Medicine at Mount Sinai Morningside/Beth Israel Hospitals, New York City, NY-10025, USA

2Department of Internal Medicine, State University of New York, Downstate Health Sciences University, Brooklyn, NY 11203, USA

3Department of Internal Medicine, Columbia College of Physicians and Surgeons, NYC Health and Hospitals/Harlem Hospital Center, Harlem, New York 10037, USA

4Division of Hematology-Oncology, Department of Internal Medicine, Albert Einstein College of medicine/ Jacobi Medical Center, Bronx, New York 10461, USA

5Trinity School of Medicine, 925 Woodstock Road, Roswell, GA 30075, USA

Pub. Date: February 03, 2021

Cite this paper

Pramod Theetha Kariyanna, Naseem A. Hossain, Neema Jayachamarajapura Onkaramurthy, Apoorva Jayarangaiah, Nimrah A. Hossain, Amog Jayarangaiah and Isabel M. McFarlane. Hypereosinophilia and Löffler’s Endocarditis: A Systematic Review. American Journal of Medical Case Reports. 2021; 9(4):241-248. doi: 10.12691/AJMCR-9-4-10

Abstract

Löffler endocarditis is an uncommon, but known complication of hypereosinophilic syndrome (HES). It is a relatively rare entity, and remains poorly understood. To this point in time, the compendium of knowledge about this disease consists of various case reports, prospective studies and review articles. We aim to present a scoping study about this disease. Our goals are to identify the characteristic features found in case reports to identify characteristic features found in patients with Löffler endocarditis as a result of hypereosinophilic syndrome. An analysis of the 26 case reports showed a mean age of 41.6 years with a standard deviation of 17.1 years. Dyspnea was the most common presenting complaint (64%) followed by fatigue (23%), cough (19%), fever (19%), orthopnea/paroxysmal nocturnal dyspnea (19%), stroke related symptoms (15%), chest pain (15%) and lower extremity edema (15%). The most common cardiac structure affected was the mitral valve (65%), followed by the tricuspid valve (42%), left ventricle (23%), with 35% of cases having involvement of two valves. The most common therapeutic modality was immunosuppression (85%), followed by anticoagulation (73%) and mitral valve replacement (23%). Death was reported in 19% of the cases. Löffler’s endocarditis continues to be associated with high morbidity and mortality. Further research must aim to develop guidelines for management of this uncommon manifestation of hypereosinophilic syndrome.

Keywords

hypereosinophilia, hypereosinophilic endocarditis, heart valves involvement, tissue diagnosis of hypereosinophilic endocarditis, associated comorbitities, prognosis

Copyright

Creative CommonsThis work is licensed under a Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

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