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异常球蛋白血症性神经病中神经滋养血管的微血管病变

Microangiopathy of vasa nervorum in dysglobulinemic neuropathy.

作者信息

Powell H C, Rodriguez M, Hughes R A

出版信息

Ann Neurol. 1984 Apr;15(4):386-94. doi: 10.1002/ana.410150414.

Abstract

Thickening of vessel walls resulting from endothelial proliferation was observed in the vasa nervorum of eleven patients with peripheral neuropathy associated with dysglobulinemia. Electron microscopy showed endothelial proliferation accompanied by abnormal accumulation of masses of intracytoplasmic filaments in each case. Of the eleven patients with dysglobulinemia, nine had monoclonal gammopathy and two were found to have polyclonal elevation of gamma globulin levels. Symptoms of neuropathy characteristically preceded detection of serum protein abnormalities by months to years. Nerve fiber lesions involved primarily the axon in four cases; segmental demyelination was the principal abnormality in the other seven. Both abnormalities were present to some degree in all eleven patients. Biphasic myelinopathy with uniform separation of myelin lamellae attributable to globulin deposition was observed in four cases. The microvascular changes included endothelial cytoplasmic enlargement, virtually obliterating the vessel lumen in many instances, with thickening of pericytes, in which intracytoplasmic filaments were prominent and pinocytotic vesicles numerous. No extracellular filaments were noted, and amyloid stains were negative. Possible effects of these microvascular changes include ischemia resulting from severe vascular luminal narrowing, and altered vascular permeability. Severe loss of axons in this group of neuropathies may be the result of ischemia, whereas altered vascular permeability may admit globulin into the endoneurium, where it may directly affect the myelin sheath and precipitate demyelination.

摘要

在11例伴有球蛋白异常血症的周围神经病患者的神经滋养血管中,观察到因内皮细胞增殖导致的血管壁增厚。电子显微镜检查显示,每例均有内皮细胞增殖,并伴有大量胞质内细丝的异常积聚。在这11例球蛋白异常血症患者中,9例有单克隆丙种球蛋白病,2例发现γ球蛋白水平呈多克隆升高。神经病症状通常在血清蛋白异常检测前数月至数年出现。神经纤维病变在4例中主要累及轴突;节段性脱髓鞘是其他7例的主要异常。在所有11例患者中,两种异常均有不同程度的存在。4例观察到因球蛋白沉积导致髓鞘板均匀分离的双相性髓鞘病。微血管变化包括内皮细胞质增大,在许多情况下几乎使管腔闭塞,周细胞增厚,其中胞质内细丝突出,吞饮小泡众多。未发现细胞外细丝,淀粉样染色为阴性。这些微血管变化的可能影响包括严重血管腔狭窄导致的缺血,以及血管通透性改变。这组神经病中轴突的严重丧失可能是缺血的结果,而血管通透性改变可能使球蛋白进入神经内膜,在那里它可能直接影响髓鞘并促使脱髓鞘。

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