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A Case of Rhabdomyolysis in Eosinophilic Polymyositis / 대한신장학회잡지
Article en Ko | WPRIM | ID: wpr-102793
Biblioteca responsable: WPRO
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: 1 Índice: WPRIM Asunto principal: Biopsia Límite: Humans / Male Idioma: Ko Revista: Korean Journal of Nephrology Año: 2001 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Asunto principal: Biopsia Límite: Humans / Male Idioma: Ko Revista: Korean Journal of Nephrology Año: 2001 Tipo del documento: Article