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糖尿病性多发性神经病变中纤维丧失的空间分布提示存在局部缺血。

The spatial distribution of fiber loss in diabetic polyneuropathy suggests ischemia.

作者信息

Dyck P J, Karnes J L, O'Brien P, Okazaki H, Lais A, Engelstad J

出版信息

Ann Neurol. 1986 May;19(5):440-9. doi: 10.1002/ana.410190504.

Abstract

Characterization and quantitation of the spatial distribution of pathological abnormalities along the length of nerves may be helpful in understanding the underlying mechanisms of diabetic polyneuropathy. To this end, by examining transverse sections of nerve roots and proximal-to-distal levels of lower limb nerves in 9 controls and 15 diabetic patients with polyneuropathy, we have determined the myelinated fiber (MF) number, size distribution, median diameter, and variability of density (MFs/mm2) among frames and among fascicles. Even in cases with mild polyneuropathy, fiber loss, a decrease in the median diameter, and an increase in the variability of density among frames and among fascicles began in proximal nerve and extended to distal levels. Multifocal fiber loss along the length of nerves and sprouting provide the best explanation for these findings. The pattern is dissimilar from that observed in diffuse metabolic disease of Schwann cells, neuronal degeneration, and dying-back neuropathy, but like that found in experimental ischemic neuropathy induced by embolization of nerve capillaries.

摘要

对沿神经长度的病理异常空间分布进行表征和定量,可能有助于理解糖尿病性多发性神经病的潜在机制。为此,通过检查9名对照者和15名患有多发性神经病的糖尿病患者的神经根横断面以及下肢神经从近端到远端各水平,我们确定了有髓纤维(MF)数量、大小分布、中位直径以及各视野间和各束间密度的变异性(MFs/mm²)。即使在轻度多发性神经病病例中,纤维丢失、中位直径减小以及各视野间和各束间密度变异性增加也始于近端神经并延伸至远端水平。沿神经长度的多灶性纤维丢失和芽生为这些发现提供了最佳解释。这种模式与在施万细胞弥漫性代谢疾病、神经元变性和轴索性神经病中观察到的模式不同,但与神经毛细血管栓塞诱导的实验性缺血性神经病中发现的模式相似。

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