횡문근 융해증을 동반한 호산구성 다발성 근염 1예

A 45-year-old man presented with muscle pain, skin nodules and persistent hypereosinophilia over a period of 4 months. Laboratory data excluded the diagnosis of trichinosis or any other parasite infection. The patient's course of the disease over the 9 months was compatible with idiopathic hype...

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Published inKidney research and clinical practice pp. 932 - 935
Main Authors 김미영, 황인석, 유홍선, 박자영, 서보경, 이상익
Format Journal Article
LanguageKorean
Published 대한신장학회 01.09.2001
Subjects
내과학
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Summary:A 45-year-old man presented with muscle pain, skin nodules and persistent hypereosinophilia over a period of 4 months. Laboratory data excluded the diagnosis of trichinosis or any other parasite infection. The patient's course of the disease over the 9 months was compatible with idiopathic hypereosinophilic syndrome. In a muscle biopsy, eosinophilic and lymphoplasma cells are predominantly infiltrated. Authors report a case of rhabdomyolysis due to eosinophilic polymyositis in idiopathic hypereosinophilic syndrome. KCI Citation Count: 1
Bibliography:G704-000889.2001.20.5.027
ISSN:2211-9132
2211-9140