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慢性炎症性脱髓鞘性多发性神经病:42例周围神经活检的免疫病理学和超微结构研究

Chronic inflammatory demyelinating polyneuropathy: immunopathological and ultrastructural study of peripheral nerve biopsy in 42 cases.

作者信息

Vital C, Vital A, Lagueny A, Ferrer X, Fontan D, Barat M, Gbikpi-Benissan G, Orgogozo J M, Henry P, Brechenmacher C, Bredin A, Desbordes P, Ribière-Bachelier C, Latinville D, Julien J, Pétry K G

机构信息

Department of Neuropathology and Neurobiologie des Affections de la Myéline, Victor Segalen University, Bordeaux, France.

出版信息

Ultrastruct Pathol. 2000 Nov-Dec;24(6):363-9. doi: 10.1080/019131200750060023.

Abstract

The authors recently reexamined the peripheral nerve biopsies from 42 patients with chronic inflammatory demyelinating polyneuropathy (CIDP). There were 27 males and 15 females, aged from 9 to 84 years, and 13 had relapses. No patient had vasculitis, monoclonal gammopathy, tumor, diabetes mellitus, Lyme disease, familial neuropathy, HIV, or any other immune deficiency. In the endoneurium, perivascular inflammatory cell infiltrates were present in only one case, but scattered histiocytes marked by KP1 on paraffin-embedded fragments were present in every case and there were no T-lymphocytes. At ultrastructural examination macrophage-associated demyelination was observed in 17 cases, of which 6 had relapses separated by intervals of several months or years. Axonal lesions without associated primary demyelination were observed in 4 cases and 3 of these had relapses. Thirty-two patients had mixed lesions of demyelination and axonal involvement. This study confirms other recent data indicating that in all cases of CIDP, macrophages are present in the endoneurium. Macrophage-associated demyelination is the characteristic feature of demyelinating forms. On the other hand, isolated primary axonal forms, which have been known since 1989, are relatively frequent and prone to relapses.

摘要

作者最近重新检查了42例慢性炎症性脱髓鞘性多发性神经病(CIDP)患者的周围神经活检样本。其中男性27例,女性15例,年龄从9岁至84岁,13例有病情复发。没有患者患有血管炎、单克隆丙种球蛋白病、肿瘤、糖尿病、莱姆病、家族性神经病、HIV或任何其他免疫缺陷。在内膜中,仅1例存在血管周围炎性细胞浸润,但在每个石蜡包埋切片中均可见散在的KP1标记的组织细胞,且无T淋巴细胞。超微结构检查发现17例有巨噬细胞相关性脱髓鞘,其中6例病情复发,复发间隔为数月或数年。4例观察到无相关原发性脱髓鞘的轴索性病变,其中3例有病情复发。32例患者有脱髓鞘和轴索受累的混合性病变。本研究证实了其他近期数据,表明在所有CIDP病例中,内膜中均存在巨噬细胞。巨噬细胞相关性脱髓鞘是脱髓鞘形式的特征性表现。另一方面,自1989年以来已知的孤立性原发性轴索形式相对常见且易于复发。

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