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复发性多软骨炎伴发脑炎后出现脑萎缩。

Relapsing Polychondritis Presented with Encephalitis Followed by Brain Atrophy.

作者信息

Ahn Suk-Won, Park Moo-Seok, Jeong Hae-Bong, Kwon Oh-Sang, Yoon Byung-Nam, Kim Hee Sung, Choi Sang Tae

机构信息

Department of Neurology, Chung-Ang University Hospital, Chung-Ang University College of Medicine, Seoul 06974, Korea.

Department of Neurology, Inha University Hospital, Inha University College of Medicine, Incheon 22332, Korea.

出版信息

Exp Neurobiol. 2017 Feb;26(1):66-69. doi: 10.5607/en.2017.26.1.66. Epub 2016 Dec 21.

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.

摘要

复发性多软骨炎(RP)是一种罕见的自身免疫性疾病,其特征是病因不明的炎症反应和软骨结构破坏。该疾病的特征性症状包括耳、鼻、喉、气管、支气管、关节、眼睛、心脏和皮肤的软骨炎症。RP合并神经症状非常罕见,与RP相关的神经受累的详细潜在机制尚未完全了解。我们在此描述了一例与RP相关的炎症性脑病变的不寻常复发病例,重点关注临床表现、自身免疫性疾病受累情况及治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fa4/5326716/6e8e84832410/en-26-66-g001.jpg

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