Idiopathic Hypereosinophilic Syndrome Presenting Acute Abdomen

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Idiopathic Hypereosinophilic Syndrome

Idiopathic hypereosinophilic syndrome is a multisystem disease with peripheral blood eosinophilia of at least 6 months duration, multiple organ system involvement, and no evidence for other known causes of eosinophilia. It is characteristically a disease of middle-aged men, often has a poor prognosis and is seldom found during childhood. Heart dicsease, characterized by endomyocardial fibrosis ...

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Idiopathic hypereosinophilic syndrome presenting as childhood hemiplegia.

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A Case of Idiopathic Hypereosinophilic Syndrome Presenting With Acute Respiratory Distress Syndrome

Although idiopathic hypereosinophilic syndrome(IHES) commonly involves the lung, it is rarely associated with acute respiratory distress syndrome (ARDS). Here we describe a case of IHES presented in conjunction with ARDS. A 37-year-old male visited the emergency department at Samsung Medical Center, Seoul, Korea, with a chief complaint of dyspnea. Blood tests showed profound peripheral eosinoph...

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Idiopathic hypereosinophilic syndrome presenting as severe Loeffler's endocarditis.

Loeffler ’s endocarditis, also known as Loeffler ’s endomyocardial disease, was first described by Wilhelm Loeffler in a patient with progressive heart failure due to eosinophilic infiltration of the endomyocardium, which was found to be secondary to peripheral eosinophilia1. It appears to be a subset of hypereosinophilic syndrome (HES), in which the heart is predominantly involved, characteriz...

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A 14 year old girl with idiopathic hypereosinophilic syndrome is described. In addition to weight loss, anaemia, amenorrhoea, general lethargy, anorexia, mouth ulcers, blisters of hands and feet, and petechial skin rash, she had features of involvement of the cardiovascular system as the major complication. She responded well to treatment. After a comprehensive search of the published reports 1...

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ژورنال

عنوان ژورنال: Internal Medicine

سال: 2007

ISSN: 0918-2918,1349-7235

DOI: 10.2169/internalmedicine.46.6309