Dickmann U, Ritter G, Kretzschmar H
Nervenarzt. 1986 May;57(5):309-10.
We report on two patients who suffered from bullous pemphigoid and developed cerebral infarctions during the course of this autoimmune dermatosis. The first patient who had a bullous dermatosis for three weeks presented with a sudden paresis of her right arm. She improved under steroid therapy and developed a left sided hemiparesis after steroids were reduced for diagnostic purposes. The second patient developed signs of brain stem infarction during the course of full-blown bullous pemphigoid. Neither patient had known risk factors, signs of atherosclerosis or cardiac embolism. Both patients improved with steroids and azathioprine.
我们报告了两名患有大疱性类天疱疮的患者,他们在这种自身免疫性皮肤病的病程中发生了脑梗死。第一名患者患有大疱性皮肤病三周,突然出现右臂麻痹。她在接受类固醇治疗后病情好转,但为了诊断目的减少类固醇用量后出现了左侧偏瘫。第二名患者在典型的大疱性类天疱疮病程中出现了脑干梗死的症状。两名患者均无已知的危险因素、动脉粥样硬化迹象或心脏栓塞。两名患者使用类固醇和硫唑嘌呤后病情均有改善。