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吉兰-巴雷综合征患者脊髓中的炎性浸润。

Inflammatory infiltrates in the spinal cord of patients with Guillain-Barré syndrome.

作者信息

Müller H D, Beckmann A, Schröder J M

机构信息

Institut für Neuropathologie, Universitätsklinikum der Rheinisch-Westfälischen Hochschule Aachen, Pauwelsstr 30, 52074, Aachen, Germany.

出版信息

Acta Neuropathol. 2003 Dec;106(6):509-17. doi: 10.1007/s00401-003-0768-0. Epub 2003 Sep 17.

DOI:10.1007/s00401-003-0768-0
PMID:13680278
Abstract

Guillain-Barré syndrome (GBS) is defined as an acute inflammatory demyelinating polyradiculoneuropathy (AIDP) of the peripheral nervous system. Reports on central nervous system involvement in patients with GBS are rare and the histopathological analysis was usually restricted to conventional staining techniques. We were able to investigate four cases with GBS at autopsy in respect to the inflammatory infiltrates and histopathological changes in the spinal cord by immunohistochemistry using a panel of antibodies recognizing lymphocytes and different macrophage-activation antigens. There were increased inflammatory cell infiltrates comprising lymphocytes and macrophages in the spinal cord of two cases. In one of these two cases, GBS predominantly affecting the motor system similar to acute motor axonal neuropathy (AMAN) developed following hepatitis B vaccination; in the second one, GBS developed rapidly 4 days after onset of intravenous purified GM1-ganglioside application affecting the motor as well as the sensory system, resembling acute motor sensory axonal neuropathy (AMSAN). Impairment of the spinal anterior horn cells with their axons was suggested to be responsible for prolonged motor symptoms and the predominantly axonal type of neuropathy at least as a late-stage feature in these two cases with fatal outcome. Insignificant cellular infiltrates in the spinal cord were noted in the other two GBS cases. Focal cellular infiltration of spinal nerve roots and meninges was similar in all cases.

摘要

吉兰-巴雷综合征(GBS)被定义为一种外周神经系统的急性炎症性脱髓鞘性多发性神经根神经病(AIDP)。关于GBS患者中枢神经系统受累的报道很少,组织病理学分析通常局限于传统染色技术。我们能够通过使用一组识别淋巴细胞和不同巨噬细胞激活抗原的抗体进行免疫组织化学,对4例GBS患者进行尸检,以研究脊髓中的炎性浸润和组织病理学变化。两例患者的脊髓中炎性细胞浸润增加,包括淋巴细胞和巨噬细胞。在这两例患者中,其中一例在接种乙肝疫苗后发生了主要影响运动系统的GBS,类似于急性运动轴索性神经病(AMAN);另一例在静脉注射纯化的GM1神经节苷脂4天后迅速发生GBS,影响运动和感觉系统,类似于急性运动感觉轴索性神经病(AMSAN)。这两例预后致命的患者,脊髓前角细胞及其轴突的损伤被认为是导致运动症状持续以及主要为轴索性神经病的原因,至少在晚期是如此。另外两例GBS患者的脊髓中细胞浸润不明显。所有病例中脊髓神经根和脑膜的局灶性细胞浸润情况相似。

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