Fukutani Y, Katsukawa K, Matsubara R, Kobayashi K, Nakamura I, Yamaguchi N
Division of Neuropsychiatry, National Sanatorium Hokuriku Hospital, Toyama, Japan.
J Neurol Neurosurg Psychiatry. 1993 Nov;56(11):1207-12. doi: 10.1136/jnnp.56.11.1207.
Three Japanese patients with Joseph disease from different families developed sleep disturbance, followed by delirium at the middle to end stage. Brain CT scans of the three patients showed brainstem tegmental atrophy. EEG revealed slowing of background activity. Two necropsy cases showed degeneration of the reticular formation, raphe nuclei and locus ceruleus in the brainstem tegmentum in addition to the common pathological findings of Joseph disease. The clinicopathological correlation between the delirium and the brainstem tegmental atrophy in Joseph disease is discussed.
三名来自不同家族的患有约瑟夫病的日本患者出现睡眠障碍,随后在疾病中晚期出现谵妄。这三名患者的脑部CT扫描显示脑干被盖萎缩。脑电图显示背景活动减慢。两例尸检病例显示,除了约瑟夫病常见的病理表现外,脑干被盖中的网状结构、中缝核和蓝斑也出现了退化。本文讨论了约瑟夫病中谵妄与脑干被盖萎缩之间的临床病理相关性。