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Relapsing Polychondritis Presented with Encephalitis Followed by Brain Atrophy
Article in English | WPRIM (Western Pacific) | ID: wpr-30375
Responsible library: WPRO
ABSTRACT
Relapsing polychondritis (RP) is a rare autoimmune disease that is characterized by inflammatory reaction of unknown etiology and destruction of cartilaginous structures. Characteristic symptoms of this disease include cartilage inflammation of the ear, nose, larynx, trachea, bronchi, joints, eyes, heart and skin. Concomitance with neurologic symptom is very rare in RP, and the detailed underlying mechanism of neurological involvement associated with RP is not fully understood. We herein described an unusual recurrent case of inflammatory brain lesions associated with RP, with attention to clinical manifestations, autoimmune disease involvement, and therapeutic effects.
Subject(s)

Full text: Available Database: WPRIM (Western Pacific) Main subject: Polychondritis, Relapsing / Atrophy / Skin / Autoimmune Diseases / Trachea / Brain / Bronchi / Cartilage / Nose / Neuromyelitis Optica Language: English Journal: Experimental Neurobiology Year: 2017 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Main subject: Polychondritis, Relapsing / Atrophy / Skin / Autoimmune Diseases / Trachea / Brain / Bronchi / Cartilage / Nose / Neuromyelitis Optica Language: English Journal: Experimental Neurobiology Year: 2017 Document type: Article
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