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无脉症又名Takayasa氏动脉炎或主动脉弓综合征。多见于青年女性,合并颈内动脉闭塞者少见,现将我科遇到的一例报告如下。患者,女,27岁。因右侧肢体活动不灵1d入院。在2d前下午,感全身乏力,随即出现嘴歪,右口角流涎,当日晚餐时右手无力,持筷困难,入夜后右下肢无力。翌晨,说话不清,右下肢麻木。无发热、头痛、眩晕、恶心呕吐等。自18岁始有发作性右眼发花,视物不清,少则每天发作1~2次,多则每天发作4~5次。每次发作可持续几秒钟至数十分种,发作过后如常人。查体:双侧颈动脉搏动正
Pulse-free disease Also known as Takayasa’s arteritis or aortic arch syndrome. More common in young women, combined with internal carotid artery occlusion are rare, now we encounter a case report is as follows. Patient, female, 27 years old. Physical activity on the right hand 1d admission. In the afternoon before 2d, the feeling of weakness, then there mouth crooked, right mouth drool, right hand during dinner weakness, difficulty holding chopsticks, right lower limb weakness after the night. The next morning, unclear, right lower limb numbness. No fever, headache, dizziness, nausea and vomiting. Since the age of 18 has episodic onset of right eye, blurred vision, ranging from 1 to 2 episodes per day, as many as 4 to 5 episodes per day. Each attack can last for a few seconds to dozens of species, such as normal people after the attack. Physical examination: bilateral carotid pulse positive