Cavaletti G, Petruccioli M G, Crespi V, Pioltelli P, Marmiroli P, Tredici G
Department of Neurology V, University of Milan, Italy.
J Neurol Neurosurg Psychiatry. 1990 Oct;53(10):886-9. doi: 10.1136/jnnp.53.10.886.
Ten patients with essential cryoglobulinaemia type II were examined for peripheral nerve damage. In six cases distal symmetrical nerve involvement was present, while in three other cases abnormalities restricted to single nerves were found. Electrophysiological and morphological data were consistent with axonal damage, the larger myelinated fibres being most affected. Although active signs of vasculitis and immunoperoxidase staining for immunoglobulins were not present, endoneurial vessels were widely damaged, with abnormally thick endothelial cells and redundant basal membranes. These findings, together with a patchy distribution of myelinated fibre loss, suggest ischaemia as a cause of peripheral neuropathy during essential cryoglobulinaemia type II. A follow up examination, performed one year after haematologial remission, revealed that no further peripheral nerve damage had occurred.
对10例II型原发性冷球蛋白血症患者进行了周围神经损伤检查。6例出现远端对称性神经受累,另外3例发现异常局限于单条神经。电生理和形态学数据与轴索损伤一致,较大的有髓纤维受影响最严重。尽管不存在血管炎的活跃迹象和免疫球蛋白免疫过氧化物酶染色,但神经内膜血管广泛受损,内皮细胞异常增厚,基底膜冗余。这些发现,连同有髓纤维丢失的斑片状分布,提示缺血是II型原发性冷球蛋白血症期间周围神经病变的一个原因。血液学缓解一年后进行的随访检查显示,未发生进一步的周围神经损伤。