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伴有小脑齿状核神经元肿胀的迟发性运动障碍。病例报告及形态计量学研究。

Tardive dyskinesia with inflated neurons of the cerebellar dentate nucleus. Case reports and morphometric study.

作者信息

Arai N, Amano N, Iseki E, Yokoi S, Saito A, Takekawa Y, Misugi K

出版信息

Acta Neuropathol. 1987;73(1):38-42. doi: 10.1007/BF00695500.

Abstract

Four autopsied cases of tardive dyskinesia manifesting oral hyperkinesia revealed markedly inflated neurons in the cerebellar dentate nucleus (DN), which had not been described previously. The inflation of the neurons was proved to be statistically significant (P less than 0.01) by morphometric study. The nuclei were usually situated in the central portion of the cytoplasm. This inflated change was different from both central chromatolysis and grumose degeneration of the DN, typically observed in progressive supranuclear palsy and dentatorubropallidolysian atrophy, and seemed to be easy to miss without careful observation, since neuronal loss and gliosis were very mild in the DN. Among a few autopsied cases of tardive dyskinesia reported previously, degeneration of the DN was described in only two. It is believed, however, that the inflated neurons of the DN may not be so rare and may be related to the occurrence of some involuntary hyperkinesia, especially oral hyperkinesia following some neurotoxic disorders and/or neuroleptic medications.

摘要

4例表现为口部运动亢进的迟发性运动障碍尸检病例显示,小脑齿状核(DN)中有明显肿胀的神经元,这在之前未曾有过描述。通过形态计量学研究证实,神经元的肿胀具有统计学意义(P小于0.01)。细胞核通常位于细胞质的中央部分。这种肿胀变化不同于在进行性核上性麻痹和齿状核红核苍白球萎缩中典型观察到的DN中央染色质溶解和颗粒样变性,而且由于DN中的神经元丢失和胶质细胞增生非常轻微,如果不仔细观察似乎很容易被忽略。在之前报道的少数迟发性运动障碍尸检病例中,仅在2例中描述了DN的变性。然而,据信DN中肿胀的神经元可能并非如此罕见,可能与某些不自主运动亢进的发生有关,尤其是在一些神经毒性疾病和/或抗精神病药物治疗后出现的口部运动亢进。

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