Berkovic S F, Karpati G, Carpenter S, Lang A E
Montreal Neurological Institute, Quebec, Canada.
Arch Neurol. 1987 Nov;44(11):1184-7. doi: 10.1001/archneur.1987.00520230064016.
Three unrelated patients, aged 4, 18, and 47 years, had generalized dystonia associated with bilateral striatal hypodensities on computed tomography. Mitochondrial encephalopathy was considered to be the most likely diagnosis, but this could not be proved. These patients confirm previous reports linking acquired generalized dystonia with bilateral putaminal lesions and they highlight the problem in differential diagnosis of this clinicoradiologic syndrome.
三名互不相关的患者,年龄分别为4岁、18岁和47岁,患有全身性肌张力障碍,计算机断层扫描显示双侧纹状体低密度。线粒体脑病被认为是最可能的诊断,但无法得到证实。这些患者证实了先前将获得性全身性肌张力障碍与双侧壳核病变联系起来的报告,并且突出了这种临床放射学综合征鉴别诊断中的问题。