Sugita Y, Yokochi M, Ida A, Mori H, Shirai T, Imai H, Mizuno Y
Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan.
No To Shinkei. 1996 Oct;48(10):963-71.
We report a 43-year-old woman who died after 18 years history of parkinsonism. She was well until 25 years of the age (1976) when she noted a difficulty in stepping her feet. In the next year, she started to drag her feet. She was treated with levodopa with good response, however, she developed dyskinesia when she was 33 years of the age. She was evaluated in another hospital in 1984. She showed normal intelligence, normal ocular movement, masked face, small voice, small step gait, stooped posture, freezing of the gait, retropulsion, and cogwheel rigidity in limbs. No tremor or ataxia was noted. She received left ventrolateral thalamotomy at that time. Rigidity on the right side markedly reduced, however, she continued to show bradykinesia and motor fluctuations. On August 1 of 1994, she developed fever of 40 degrees C and dyspnea. On the next day, she expired from acute respiratory distress. She was able to walk unsupported until just before her last admission. The patient was discussed in a neurological CPC. The chief discussant arrived at the conclusion that this patient had Lewy body-positive young onset Parkinson's disease. Opinions were divided into two groups, i.e., young onset Lewy-body positive Parkinson's disease and Lewy-body negative young onset parkinsonism. Post-mortem examination revealed moderate loss of pigmented neurons in the substantia nigra more in the ventro-lateral part. Lewy bodies were found in the remaining neurons. Lewy bodies were more frequently seen in the locus coeruleus, although neuronal loss was less prominent in the locus coeruleus. The dorsal vagal motor nucleus showed moderate loss of neurons. Otherwise, the central nervous system was unremarkable. To our knowledge, this patient had the second youngest age of the onset so far reported in the literature for Lewy-body positive typical Parkinson's disease.
我们报告一名43岁患有帕金森病18年的女性患者,其最终死亡。她在25岁(1976年)之前情况良好,当时她注意到脚步移动困难。次年,她开始拖脚行走。她接受左旋多巴治疗,反应良好,但在33岁时出现了运动障碍。1984年她在另一家医院接受评估。她表现出智力正常、眼球运动正常、面具脸、声音细小、小步步态、弯腰姿势、步态冻结、后冲以及肢体齿轮样强直。未发现震颤或共济失调。当时她接受了左侧丘脑腹外侧核切开术。右侧的强直明显减轻,但她仍持续表现出运动迟缓及运动波动。1994年8月1日,她出现40摄氏度的发热及呼吸困难。次日,她因急性呼吸窘迫死亡。直到最后一次入院前,她仍能独立行走。该病例在一次神经科临床病理讨论会上进行了讨论。主要讨论者得出结论,该患者患有路易体阳性的早发型帕金森病。意见分为两组,即早发型路易体阳性帕金森病和路易体阴性早发型帕金森综合征。尸检显示黑质中色素神经元有中度缺失,腹外侧部分更为明显。在剩余的神经元中发现了路易小体。虽然蓝斑核中神经元丢失不太明显,但路易小体在蓝斑核中更常见。迷走神经背运动核显示神经元有中度缺失。除此之外,中枢神经系统未见明显异常。据我们所知,该患者是文献中迄今报道的路易体阳性典型帕金森病发病年龄第二小的病例。