Gilman S, Low P A, Quinn N, Albanese A, Ben-Shlomo Y, Fowler C J, Kaufmann H, Klockgether T, Lang A E, Lantos P L, Litvan I, Mathias C J, Oliver E, Robertson D, Schatz I, Wenning G K
Department of Neurology, University of Michigan Medical Center, Ann Arbor 48109-0316, USA.
J Neurol Sci. 1999 Feb 1;163(1):94-8. doi: 10.1016/s0022-510x(98)00304-9.
We report the results of a consensus conference on the diagnosis of multiple system atrophy (MSA). We describe the clinical features of the disease, which include four domains: autonomic failure/urinary dysfunction, parkinsonism and cerebellar ataxia, and corticospinal dysfunction. We set criteria to define the relative importance of these features. The diagnosis of possible MSA requires one criterion plus two features from separate other domains. The diagnosis of probable MSA requires the criterion for autonomic failure/urinary dysfunction plus poorly levodopa responsive parkinsonism or cerebellar ataxia. The diagnosis of definite MSA requires pathological confirmation.
我们报告了一次关于多系统萎缩(MSA)诊断的共识会议结果。我们描述了该疾病的临床特征,包括四个方面:自主神经功能衰竭/排尿功能障碍、帕金森综合征和小脑共济失调,以及皮质脊髓功能障碍。我们制定了标准来界定这些特征的相对重要性。可能的MSA诊断需要一条标准加上来自其他不同方面的两个特征。很可能的MSA诊断需要自主神经功能衰竭/排尿功能障碍的标准加上对左旋多巴反应不佳的帕金森综合征或小脑共济失调。确诊的MSA诊断需要病理证实。