Cargando…

Syndrome d’hyperéosinophilie avec atteinte cardiaque

We report the case of a 30-year old man with no previous medical history and without cardiovascular risk factors, hospitalized for NYHA Class IV dyspnoea associated with palpitations in the Department of Cardiology. Clinical examination showed signs of cardiac decompensation. The patient didn't...

Descripción completa

Detalles Bibliográficos
Autores principales: Zairi, Ihsen, Mzoughi, Khadija
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6011009/
https://www.ncbi.nlm.nih.gov/pubmed/29942409
http://dx.doi.org/10.11604/pamj.2017.28.270.14316
_version_ 1783333713206050816
author Zairi, Ihsen
Mzoughi, Khadija
author_facet Zairi, Ihsen
Mzoughi, Khadija
author_sort Zairi, Ihsen
collection PubMed
description We report the case of a 30-year old man with no previous medical history and without cardiovascular risk factors, hospitalized for NYHA Class IV dyspnoea associated with palpitations in the Department of Cardiology. Clinical examination showed signs of cardiac decompensation. The patient didn't have fever, hepatosplenomegaly and palpable lymphadenopathies. Laboratory tests showed hypereosinophilia greater than 4000 eosinophils per cubic millimeter. Electrocardiogram objectified atrial tachycardia at a rate of 100 beats per minute. Echocardiographic examination showed good left ventricular function, dilation of both atria and a thrombus filling the right ventricular apex. The diagnosis of thrombus lining the ventricular apex was suspected (A, B); successive exams showed progressive filling of the right ventricular apex. Cardiac MRI showed apical filling of both ventricles and after intravenous injection of gadolinium, late subendocardial enhancement in the left ventricular apex and in the right ventricular apex, suggesting fibrosis (C, D). Etiologic investigation of hypereosinophilia excluded parasitic diseases, drug therapies, neoplasias and autoimmune diseases as a cause. The diagnosis of idiopathic hypereosinophilic syndrome associated with cardiac involvement was retained. Corticosteroid therapy associated with hydroxyurea therapy and long-term anticoagulant therapy were started. Patient's evolution was gradually favorable with disappearance of hypereosinophilia.
format Online
Article
Text
id pubmed-6011009
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher The African Field Epidemiology Network
record_format MEDLINE/PubMed
spelling pubmed-60110092018-06-25 Syndrome d’hyperéosinophilie avec atteinte cardiaque Zairi, Ihsen Mzoughi, Khadija Pan Afr Med J Images in Medicine We report the case of a 30-year old man with no previous medical history and without cardiovascular risk factors, hospitalized for NYHA Class IV dyspnoea associated with palpitations in the Department of Cardiology. Clinical examination showed signs of cardiac decompensation. The patient didn't have fever, hepatosplenomegaly and palpable lymphadenopathies. Laboratory tests showed hypereosinophilia greater than 4000 eosinophils per cubic millimeter. Electrocardiogram objectified atrial tachycardia at a rate of 100 beats per minute. Echocardiographic examination showed good left ventricular function, dilation of both atria and a thrombus filling the right ventricular apex. The diagnosis of thrombus lining the ventricular apex was suspected (A, B); successive exams showed progressive filling of the right ventricular apex. Cardiac MRI showed apical filling of both ventricles and after intravenous injection of gadolinium, late subendocardial enhancement in the left ventricular apex and in the right ventricular apex, suggesting fibrosis (C, D). Etiologic investigation of hypereosinophilia excluded parasitic diseases, drug therapies, neoplasias and autoimmune diseases as a cause. The diagnosis of idiopathic hypereosinophilic syndrome associated with cardiac involvement was retained. Corticosteroid therapy associated with hydroxyurea therapy and long-term anticoagulant therapy were started. Patient's evolution was gradually favorable with disappearance of hypereosinophilia. The African Field Epidemiology Network 2017-11-28 /pmc/articles/PMC6011009/ /pubmed/29942409 http://dx.doi.org/10.11604/pamj.2017.28.270.14316 Text en © Ihsen Zairi et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Images in Medicine
Zairi, Ihsen
Mzoughi, Khadija
Syndrome d’hyperéosinophilie avec atteinte cardiaque
title Syndrome d’hyperéosinophilie avec atteinte cardiaque
title_full Syndrome d’hyperéosinophilie avec atteinte cardiaque
title_fullStr Syndrome d’hyperéosinophilie avec atteinte cardiaque
title_full_unstemmed Syndrome d’hyperéosinophilie avec atteinte cardiaque
title_short Syndrome d’hyperéosinophilie avec atteinte cardiaque
title_sort syndrome d’hyperéosinophilie avec atteinte cardiaque
topic Images in Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6011009/
https://www.ncbi.nlm.nih.gov/pubmed/29942409
http://dx.doi.org/10.11604/pamj.2017.28.270.14316
work_keys_str_mv AT zairiihsen syndromedhypereosinophilieavecatteintecardiaque
AT mzoughikhadija syndromedhypereosinophilieavecatteintecardiaque