Katada E, Ojika K, Uemura M, Maeno K, Mitake S, Tsugu Y, Otsuka Y, Iwase T
Second Department of Internal Medicine, Nagoya City University Medical School.
Intern Med. 1997 Feb;36(2):118-24. doi: 10.2169/internalmedicine.36.118.
A rare case of mixed connective tissue disease (MCTD) with acute polyradiculoneuropathy is reported. A 23-year-old woman presented with high body temperature, arthralgia and a headache, and developed gait disturbance two weeks later. She had many clinical features common to patients with MCTD. Her neurological manifestations were diagnosed as acute polyradiculoneuropathy based on the clinical picture, combined with supportive ancillary data, including cerebrospinal fluid (CSF) analysis, electrophysiological evaluation, sural nerve biopsy, peroneus brevis muscle biopsy, and magnetic resonance imaging (MRI). Her neurologic deficits, as well as associated laboratory findings, were improved by corticosteroid therapy.
报告了一例罕见的混合性结缔组织病(MCTD)合并急性多发性神经根神经病。一名23岁女性出现高热、关节痛和头痛,两周后出现步态障碍。她有许多MCTD患者常见的临床特征。根据临床表现,结合脑脊液(CSF)分析、电生理评估、腓肠神经活检、短腓骨肌活检和磁共振成像(MRI)等辅助支持数据,其神经学表现被诊断为急性多发性神经根神经病。皮质类固醇治疗改善了她的神经功能缺损以及相关实验室检查结果。