Chemmanam Thomas, Pandian Jeyaraj D, Kadyan Randhir S, Bhatti S M
Department of Neurology, Christian Medical College, Ludhiana, Punjab, India.
J Clin Neurosci. 2007 Jan;14(1):94-6. doi: 10.1016/j.jocn.2005.11.041. Epub 2006 Oct 27.
We describe a patient with Ross syndrome who had the classic triad of segmental anhidrosis, tonic pupils and hyporeflexia. Dilute pilocarpine (0.1%) instillation in both eyes revealed parasympathetic denervation hypersensitivity. There was evidence of cardiac dysautonomia in the form of a decrease in heart rate variability with deep breathing and an abnormal Valsalva response. A thermoregulatory sweat test showed the presence of sweating in the right cheek, neck and upper one-third of the left arm and shoulder only. Sympathetic skin responses were absent in the affected segments of the upper limb. Ross syndrome is a degenerative disorder that progressively involves different fibre populations, starting with autonomic fibres and then involving the unmyelinated and myelinated sensory fibres. A careful clinical examination and simple bedside autonomic tests can confirm the diagnosis.
我们描述了一名患有罗斯综合征的患者,其具有节段性无汗、强直性瞳孔和反射减退这一典型三联征。双眼滴入稀释的毛果芸香碱(0.1%)显示出副交感神经去神经超敏反应。有证据表明存在心脏自主神经功能障碍,表现为深呼吸时心率变异性降低以及瓦尔萨尔瓦动作反应异常。温热调节性发汗试验显示仅右侧脸颊、颈部以及左臂和肩部上三分之一处有出汗。上肢受累节段的交感神经皮肤反应缺失。罗斯综合征是一种退行性疾病,最初累及自主神经纤维,随后逐渐累及无髓鞘和有髓鞘的感觉纤维,不同纤维群会逐渐受到影响。仔细的临床检查和简单的床边自主神经测试即可确诊。