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药物性弥漫性脑轴索性白质脑病尸检病例:与可逆性后部白质脑病综合征相关的发病机制

An autopsy case of drug-induced diffuse cerebral axonopathic leukoencephalopathy: the pathogenesis in relation to reversible posterior leukoencephalopathy syndrome.

作者信息

Okeda Riki, Kawamoto Tatsunari, Tanaka Eri, Shimizu Hideo

机构信息

Department of Pathology, Kawasaki-Saiwai Hospital, Kawasaki-shi, Kanagawa-ken, Japan.

出版信息

Neuropathology. 2007 Aug;27(4):364-70. doi: 10.1111/j.1440-1789.2007.00771.x.

Abstract

An autopsy case of diffuse axonopathic leukoencephalopathy induced by drug treatment is reported. A 70-year-old woman with multiple myeloma developed encephalopathy several days after completing a course of intravenous human immunoglobulin (IVIg) and granulocyte-colony stimulating factor (G-CSF), and died within I month. T2-weighted MRI demonstrated multifocal high-signal areas in the bilateral cerebral white matter, especially in the right frontal lobe. Neuropathologically, multifocal hydropic axonal swelling with a poor glial reaction was recognized diffusely in the bilateral deep cerebral white matter, being especially marked in the frontal lobe. The cortex, subcortical U-fibers, corpus callosum, and anterior commissure were spared. The cerebellar white matter also showed similar changes, albeit less marked, but the brainstem was spared. Microscopically, the myeloma involvement of the CNS was limited to the dura, and the cerebral arteries showed slight atherosclerosis, but neither thrombi nor angitis. This case, although ultimately fatal, neurologically and neuroradiologically resembled reversible posterior leukoencephalopathy syndrome (RPLS) induced by IVIg and/or G-CSF, and the nature and selective distribution of the neuropathological changes suggested that the pathogenesis involved vasospasm of the bilateral internal carotid artery and the main trunks of the cerebral arteries, due to unknown cause, inducing ischemia in the deep white matter, which is supplied by long nutrient arteries.

摘要

报告了一例药物治疗引起的弥漫性轴索性白质脑病尸检病例。一名70岁的多发性骨髓瘤女性在完成静脉注射人免疫球蛋白(IVIg)和粒细胞集落刺激因子(G-CSF)疗程几天后出现脑病,并在1个月内死亡。T2加权磁共振成像显示双侧脑白质出现多灶性高信号区,尤其是右侧额叶。神经病理学检查发现,双侧大脑深部白质弥漫性存在多灶性水肿性轴突肿胀,胶质反应较弱,额叶尤为明显。皮质、皮质下U形纤维、胼胝体和前连合未受累。小脑白质也有类似改变,尽管程度较轻,但脑干未受累。显微镜下,中枢神经系统的骨髓瘤累及仅限于硬脑膜,脑动脉有轻度动脉粥样硬化,但无血栓形成或血管炎。该病例虽然最终致命,但在神经学和神经放射学上类似于IVIg和/或G-CSF诱导的可逆性后部白质脑病综合征(RPLS),神经病理学改变的性质和选择性分布提示其发病机制涉及双侧颈内动脉和脑动脉主干因不明原因发生血管痉挛,导致由长营养动脉供血的深部白质缺血。

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