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Three Cases of Churg-Strauss Syndrome Diagnosed after Presence of Cutaneous Manifestation / 대한피부과학회지
Korean Journal of Dermatology ; : 62-67, 2011.
Artigo em Coreano | WPRIM | ID: wpr-171983
ABSTRACT
Churg-Strauss syndrome (CSS) is an uncommon disorder that is characterized by asthma or allergic rhinitis, fever, systemic vasculitis, extravascular granulomas and hypereosinophilia. Cutaneous manifestations of CSS are one of the most common extra-pulmonary findings, and they occur in approximately 60% of the cases. Other manifestations include pulmonary infiltrates and heart, kidney, gastrointestinal tract, peripheral and central nervous system involvement and the patients also complain of systemic symptoms, including malaise, fever, myalgia and weight loss. The diagnosis of CSS is difficult because the manifestations vary with the disease stage and delayed treatment can lead to fatal major organ damage. We report here on 3 cases of CSS that were first diagnosed by the dermatologic department and with consultation from other departments. So, we want to remind dermatologists that if the patients of asthma or other allergic diseases have purpuric skin lesion, then CSS should be included in the differential diagnosis.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Asma / Pele / Vasculite / Síndrome de Churg-Strauss / Redução de Peso / Sistema Nervoso Central / Rinite / Rinite Alérgica Perene / Trato Gastrointestinal / Diagnóstico Diferencial Tipo de estudo: Estudo diagnóstico Limite: Humanos Idioma: Coreano Revista: Korean Journal of Dermatology Ano de publicação: 2011 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Asma / Pele / Vasculite / Síndrome de Churg-Strauss / Redução de Peso / Sistema Nervoso Central / Rinite / Rinite Alérgica Perene / Trato Gastrointestinal / Diagnóstico Diferencial Tipo de estudo: Estudo diagnóstico Limite: Humanos Idioma: Coreano Revista: Korean Journal of Dermatology Ano de publicação: 2011 Tipo de documento: Artigo