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Relapsing Polychondritis Showing Personality Changes and Cognitive Impairment / 계명의대학술지
Keimyung Medical Journal ; : 133-139, 2016.
Article en Ko | WPRIM | ID: wpr-110505
Biblioteca responsable: WPRO
ABSTRACT
Relapsing polychondritis is a rare, multisystem autoimmune disease. It is characterized by recurrent inflammation of the cartilage and connective tissues in the body. In this paper, we described a case of relapsing polychondritis initially presented symptoms of cognitive dysfunction and personality changes. A 63-year-old male reprented fever, cognitive impairment and personality changes. Brain magnetic resonance imaging revealed leptomeningeal and periauricular hyperintensities. A cerebrospinal fluid examination showed aseptic meningitis. As he reprented hearing difficulties, audiometry showed the sensory neural hearing loss. On physical examination, erythematous swollen auricles were noted. Auricle biopsy consisted with inflammation with perichondritis. He was diagnosed with relapsing polychondritis accompanied by leptomeningeal meningitis, and treated with methylprednisolone (62.5 mg/day for 3 days) followed by prednisolone 60 mg/day and methotrexate 7.5 mg/week. Fever and painful swellings on the both ears subsided. He showed improvement in cognitive function and personality. Although relapsing polychondritis is rare, it should be considered to be a possible cause of leptomeningeal meningitis.
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Texto completo: 1 Índice: WPRIM Asunto principal: Examen Físico / Policondritis Recurrente / Audiometría / Enfermedades Autoinmunes / Biopsia / Encéfalo / Metilprednisolona / Prednisolona / Imagen por Resonancia Magnética / Cartílago Límite: Humans / Male Idioma: Ko Revista: Keimyung Medical Journal Año: 2016 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Asunto principal: Examen Físico / Policondritis Recurrente / Audiometría / Enfermedades Autoinmunes / Biopsia / Encéfalo / Metilprednisolona / Prednisolona / Imagen por Resonancia Magnética / Cartílago Límite: Humans / Male Idioma: Ko Revista: Keimyung Medical Journal Año: 2016 Tipo del documento: Article