Abnormal cardiovascular responses to postural changes and pharmacologic agents in a case of Shy-Drager syndrome.

J S Liu, S S Liu, W H Chan, P Y Shii, S L Howng
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Abstract

A 64-year-old carpenter had an unsteady gait, severe dizziness, nocturia, and a loss of erection for more than 4 years. The neurological manifestations consisted of a wide-based ataxic gait, bilateral dysmetria with intentional tremor, staccato speech, rigidity, bradykinesia, and an iris-thinning. There was reproducible orthostatic hypotension. A sweat test revealed severe anhidrosis. Nicotine and methylbenzene sensitivity was absent, whereas norepinephrine infusion test showed a significant elevation of blood pressure. The resting plasma norepinephrine level on recumbency was low and a subnormal surge was noted on standing or exercise. We conclude that the clinical features caused by a degenerative process involving both the central and peripheral autonomic systems, together with atrophy of other systems in this patient, constitute the Shy-Drager syndrome.

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Shy-Drager综合征一例心血管对体位改变和药物的异常反应。
一位64岁的木匠,步态不稳,严重头晕,夜尿症,勃起障碍超过4年。神经学表现包括宽基共济失调步态、双侧节律障碍伴故意震颤、言语不连贯、僵硬、运动迟缓和虹膜变薄。存在可重复的直立性低血压。汗液测试显示严重的无汗症。尼古丁和甲苯不敏感,而去甲肾上腺素输注试验显示血压明显升高。平卧时静息血浆去甲肾上腺素水平较低,站立或运动时异常增高。我们的结论是,由涉及中枢和外周自主神经系统的退行性过程引起的临床特征,以及该患者其他系统的萎缩,构成了希-德尔格综合征。
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