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A Case of Rhabdomyolysis in Eosinophilic Polymyositis / 대한신장학회잡지
Korean Journal of Nephrology ; : 932-935, 2001.
Artigo em Coreano | WPRIM | ID: wpr-102793
ABSTRACT
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.
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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Biópsia Limite: Humanos / Masculino Idioma: Coreano Revista: Korean Journal of Nephrology Ano de publicação: 2001 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Biópsia Limite: Humanos / Masculino Idioma: Coreano Revista: Korean Journal of Nephrology Ano de publicação: 2001 Tipo de documento: Artigo