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无单克隆丙种球蛋白病的周围神经病和淋巴瘤:一种新分类

Peripheral neuropathies and lymphoma without monoclonal gammopathy: a new classification.

作者信息

Vital C, Vital A, Julien J, Rivel J, deMascarel A, Vergier B, Henry P, Barat M, Reiffers J, Broustet A

机构信息

Department of Pathology, University of Bordeaux, France.

出版信息

J Neurol. 1990 Jun;237(3):177-85. doi: 10.1007/BF00314591.

Abstract

Recent progress in immunopathological studies of peripheral nerve and lymph node fragments together with 16 personal cases and numerous clinicopathological reports have suggested a new classification of peripheral neuropathies (PN) and lymphomas. These are: (1) PN due to local infiltrations by a T-cell lymphoma: (2) acute polyradiculoneuritis due to active demyelination and associated with infiltrates of a T-cell lymphoma in the epineurium, resembling Marek's disease (which is a T-cell lymphoma); (3) B-cell lymphoma proliferation which may be restricted to or predominate in the peripheral nervous system, with a large clinicopathological heterogeneity ranging from localized forms to ascending polyradiculoneuropathies; (4) angiotropic lymphoma, which is a B-cell lymphoma and may present as an acute mononeuropathy; (5) patients with acquired immunodeficiency syndrome due to lymphomatous infiltrates in the endoneurium, of which 2 cases of PN have been reported; (6) PN associated with organomegaly, endocrinopathy, M-component and skin lesions, certain cases being associated with a plasmocytoma and sometimes Castleman's disease but without any monoclonal gammopathy: (7) classic Guillain-Barré syndrome, prone to develop in patients with extraneural lymphoma but without any lymphomatous infiltrates in the peripheral nervous system; (8) certain cases (4 out of 16 in our series) where there is no clear relationship between PN and lymphoma, and there are mainly features of axonal degeneration. Inflammatory perivascular infiltrates were sometimes present in the epineurium.

摘要

周围神经和淋巴结片段免疫病理学研究的最新进展,结合16例个人病例及众多临床病理报告,提示了周围神经病(PN)和淋巴瘤的新分类。这些分类如下:(1)由T细胞淋巴瘤局部浸润引起的PN;(2)由于活跃脱髓鞘导致的急性多发性神经根神经炎,与神经外膜中T细胞淋巴瘤浸润相关,类似于马立克氏病(一种T细胞淋巴瘤);(3)B细胞淋巴瘤增殖,可能局限于周围神经系统或在其中占主导地位,临床病理异质性大,范围从局限性形式到上行性多发性神经根神经病;(4)血管中心性淋巴瘤,一种B细胞淋巴瘤,可表现为急性单神经病;(5)因神经内膜淋巴瘤浸润导致获得性免疫缺陷综合征的患者,已报告2例PN;(6)与器官肿大、内分泌病、M成分和皮肤病变相关的PN,某些病例与浆细胞瘤有关,有时与卡斯尔曼病有关,但无任何单克隆丙种球蛋白病;(7)经典格林-巴利综合征,易发生于患有神经外淋巴瘤的患者,但周围神经系统无任何淋巴瘤浸润;(8)某些病例(我们系列中的16例中有4例),其中PN与淋巴瘤之间无明确关系,主要表现为轴索性变性。神经外膜有时存在炎性血管周围浸润。

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