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一名患有坏死性血管炎并接受免疫抑制治疗的患者出现中枢神经系统原发性恶性淋巴瘤和多发性神经病。

Primary malignant lymphoma of the CNS and polyneuropathy in a patient with necrotizing vasculitis treated with immunosuppression.

作者信息

Jellinger K, Kothbauer P, Weiss R, Sunder-Plassmann E

出版信息

J Neurol. 1979 Jan 5;220(4):259-68. doi: 10.1007/BF00314150.

Abstract

A woman, aged 58, who had undergone prolonged treatment with corticosteroids for generalized necrotizing vasculitis, and had received azathioprine (Imurel) for 18 months, 4 years after discontinuing the latter treatment, developed peripheral neuropathy and a rapidly progressing cerebral disorder suggesting a basal meningeal process. CSF cytology suggested malignant lymphoma with meningeal involvement. Immunological studies showed an increase of Null-lymphocytes in the peripheral blood. Autopsy disclosed a primary malignant lymphoma of the CNS with the histological appearance of a multilocular immunoblastoma showing almost ubiquitous meningocerebral involvement. Clinical and postmortem examinations failed to demonstrate any systemic extraneural lymphoproliferative disorder. In addition, there was peripheral polyneuropathy of the axonal type with denervation atrophy of skeletal muscle, but without lymphomatous involvement of the neuromuscular system. The possible relations between primary malignant lymphomas of the CNS and previous immunosuppressive treatment of immunoinflammatory disease are discussed in view of the concept of impaired immunoregulation. The pathogenetic background of peripheral polyneuropathy is unknown.

摘要

一名58岁女性,因全身性坏死性血管炎接受了长期皮质类固醇治疗,并接受硫唑嘌呤(依木兰)治疗18个月。在停止后一种治疗4年后,出现周围神经病变和迅速进展的脑部疾病,提示有基底脑膜病变。脑脊液细胞学检查提示为恶性淋巴瘤伴脑膜受累。免疫学研究显示外周血中裸淋巴细胞增多。尸检发现中枢神经系统原发性恶性淋巴瘤,组织学表现为多房性免疫母细胞瘤,几乎累及整个脑膜脑。临床和尸检检查均未发现任何系统性神经外淋巴增殖性疾病。此外,存在轴索性周围多神经病,伴有骨骼肌失神经萎缩,但神经肌肉系统无淋巴瘤累及。鉴于免疫调节受损的概念,讨论了中枢神经系统原发性恶性淋巴瘤与既往免疫炎症性疾病免疫抑制治疗之间的可能关系。周围多神经病的发病机制尚不清楚。

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