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http://dx.doi.org/10.1016/j.jaci.2009.01.069 | DOI Listing |
J Allergy Clin Immunol
December 2020
Department of Dermatology, School of Medicine, University of Utah, Salt Lake City, Utah.
Can J Cardiol
December 2016
Department of Cardiology, Institut universitaire de cardiologie et de pneumologie de Québec, Laval University, Québec City, Québec, Canada.
Hypereosinophilic syndromes (HESs) are a group of disorders characterized by end-organ damage caused by eosinophilic infiltration. We present a patient with idiopathic HES with severe tricuspid and mitral regurgitation secondary to Loeffler's endocarditis. In addition to prednisone, imatinib therapy initially helped control the eosinophil count.
View Article and Find Full Text PDFTex Heart Inst J
March 2014
Division of Hematology, Chonbuk National University Hospital, Jeonju, Jeonbuk 561-712, Republic of Korea.
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View Article and Find Full Text PDFJ Allergy Clin Immunol
February 2013
Department of Internal Medicine, Hôpital Erasme, Institute for Medical Immunology, Université Libre de Bruxelles, Gosselies, Belgium.
Background: Hypereosinophilic syndromes (HESs) are chronic disorders that require long-term therapy to suppress eosinophilia and clinical manifestations. Corticosteroids are usually effective, yet many patients become corticosteroid refractory or develop corticosteroid toxicity. Mepolizumab, a humanized monoclonal anti-IL-5 antibody, showed corticosteroid-sparing effects in a double-blind, placebo-controlled study of FIP1L1/PDGFRA-negative, corticosteroid-responsive subjects with HESs.
View Article and Find Full Text PDFJ Am Coll Cardiol
January 2012
Division of Cardiology, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.
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