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IgM副蛋白血症性神经病变的形态学改变

Morphological changes in IgM paraproteinaemic neuropathy.

作者信息

Jacobs J M, Scadding J W

机构信息

Department of Pathology, Institute of Neurology, Queen Square, London, Great Britain.

出版信息

Acta Neuropathol. 1990;80(1):77-84. doi: 10.1007/BF00294225.

Abstract

Sural nerve biopsies were examined from two patients with neuropathy associated with IgM kappa [anti-myelin-associated glycoprotein (MAG)] paraproteinaemia. Both nerves had a moderate loss of myelinated fibres. The pathology in one was of a chronic primary demyelinating type, in the other it was associated with axonal atrophy. Widened myelin (WM) was seen in both nerves affecting over 80% and 50% of myelinated fibres, respectively. The WM was associated with deposition of material which sometimes appeared granular but could also display a highly organised pattern, an appearance not previously described in these neuropathies. Granular material was also identified at the external surface of the Schwann cells of myelinated, but not of unmyelinated, fibres. WM was seen not only at the outer lamellae (a commonly observed site) but also at terminal myelin loops at the paranode, at Schmidt Lanterman incisures and at the inner and outer mesaxon. Material was also seen on the inner (adaxonal) Schwann cell surface. These are all sites associated with the presence of MAG. Other pathological features are described, including evidence of impairment of remyelination, abnormal Schwann cell/axon specialisations and the presence of tomaculous bodies. The implications of these findings are discussed.

摘要

对两名患有与IgM κ[抗髓鞘相关糖蛋白(MAG)]副蛋白血症相关神经病变的患者进行了腓肠神经活检。两条神经均有中度有髓纤维丢失。其中一条神经的病理表现为慢性原发性脱髓鞘类型,另一条神经的病理表现与轴突萎缩有关。在两条神经中均可见髓鞘增宽(WM),分别影响超过80%和50%的有髓纤维。WM与物质沉积有关,这些物质有时呈颗粒状,但也可呈现高度有序的模式,这种表现此前在这些神经病变中未曾描述过。在有髓纤维而非无髓纤维的施万细胞外表面也发现了颗粒状物质。WM不仅见于外层板(一个常见部位),还见于结旁的终末髓鞘环、施密特-兰特尔曼切迹以及内外髓鞘系膜。在施万细胞内(轴突侧)表面也可见到物质。这些都是与MAG存在相关的部位。还描述了其他病理特征,包括再髓鞘化受损、施万细胞/轴突特化异常以及腊肠体的存在。讨论了这些发现的意义。

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