当前位置: X-MOL 学术Exp. Neurobiol. › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Relapsing Polychondritis Presented with Encephalitis Followed by Brain Atrophy.
Experimental Neurobiology ( IF 2.4 ) Pub Date : 2016-12-21 , DOI: 10.5607/en.2017.26.1.66
Suk-Won Ahn 1 , Moo-Seok Park 1 , Hae-Bong Jeong 1 , Oh-Sang Kwon 1 , Byung-Nam Yoon 2 , Hee Sung Kim 3 , Sang Tae Choi 4
Affiliation  

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.

中文翻译:

复发性多发性软骨炎伴脑炎,然后出现脑萎缩。

复发性软骨炎(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的破坏。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中很少伴有神经系统症状,与RP相关的神经系统受累的详细潜在机制尚未完全了解。我们在此描述了与RP相关的炎性脑病变的不寻常复发病例,并注意临床表现,自身免疫性疾病的侵袭和治疗效果。
更新日期:2020-08-21
down
wechat
bug