双侧纹状体苍白球齿状核钙化中的短暂性帕金森综合征
Transient parkinsonism in bilateral striopallidodentate calcinosis.
作者信息
Yoshikawa Hideto, Abe Tokinari
机构信息
Department of Pediatrics, Niigata City General Hospital, Niigata, Japan.
出版信息
Pediatr Neurol. 2003 Jul;29(1):75-7. doi: 10.1016/s0887-8994(03)00049-3.
A normally developed 12-year-old female drank a cup of tea and could not sleep that night. The next morning, symptoms suggestive of parkinsonism developed, including progressive rigidity, akinesia, and a mask-like face. These signs lasted for 10 days. Brain computed tomography revealed multiple calcification, and thus she was diagnosed as having bilateral striopallidodentate calcinosis. Patients with bilateral striopallidodentate calcinosis exhibit various movement disorders. However, there have been no reports of transient parkinsonism associated with bilateral striopallidodentate calcinosis, including in children.
一名发育正常的12岁女性喝了一杯茶，当晚无法入睡。第二天早上，出现了提示帕金森综合征的症状，包括进行性僵硬、运动不能和面具脸。这些症状持续了10天。脑部计算机断层扫描显示多处钙化，因此她被诊断为双侧纹状体苍白球齿状核钙化症。双侧纹状体苍白球齿状核钙化症患者表现出各种运动障碍。然而，尚无包括儿童在内的与双侧纹状体苍白球齿状核钙化症相关的短暂性帕金森综合征的报道。
Zotero 插件