Kuhn W F, Light P J, Kuhn S C
Department of Family Medicine, Medical College of Georgia, Augusta, USA.
Acad Emerg Med. 1995 Aug;2(8):735-8. doi: 10.1111/j.1553-2712.1995.tb03627.x.
Stiff-man syndrome is a rare neurologic disorder characterized by progressive, fluctuating muscle rigidity with painful muscle contractions affecting predominantly the back and proximal extremities. In the ED, the diagnosis can be easily overlooked and misdiagnosed as acute or chronic low back pain and muscle spasm. This syndrome is often associated with diabetes, autoimmune diseases, and cancer. This report describes an illustrative case of a 39-year-old woman who presented to the ED with a two-year history of right leg spasms and low back pain that had become so severe in the preceding two days that she was unable to ambulate. Clues to the patient's proper diagnosis coincide with the diagnostic criteria for stiff-man syndrome: the presence of a slowly progressive stiffness of the axial muscles and proximal limb muscles, making ambulation difficult; hyperlordosis of the lumbar spine; episodic spasms precipitated by jarring or sudden movement; a normal intellectual, sensory, and motor examination when not in spasm; and a marked amelioration of symptoms with the IV administration of diazepam. High-dose oral diazepam is the maintenance drug of choice.
僵人综合征是一种罕见的神经系统疾病,其特征为进行性、波动性肌肉僵硬,并伴有主要影响背部和近端肢体的疼痛性肌肉收缩。在急诊科,该诊断很容易被忽视,并被误诊为急性或慢性腰痛及肌肉痉挛。这种综合征常与糖尿病、自身免疫性疾病和癌症相关。本报告描述了一例具有代表性的病例,一名39岁女性因右腿痉挛和腰痛两年就诊于急诊科,在过去两天里病情严重到无法行走。患者正确诊断的线索与僵人综合征的诊断标准相符:轴向肌肉和近端肢体肌肉存在缓慢进展的僵硬,导致行走困难;腰椎前凸;由震动或突然运动引发的发作性痉挛;不处于痉挛状态时智力、感觉和运动检查正常;静脉注射地西泮后症状明显改善。高剂量口服地西泮是首选的维持药物。