Notermans N C, Wokke J H, van der Graaf Y, Franssen H, van Dijk G W, Jennekens F G
Department of Neuromuscular Diseases, University Hospital, Utrecht, The Netherlands.
J Neurol Neurosurg Psychiatry. 1994 Dec;57(12):1525-7. doi: 10.1136/jnnp.57.12.1525.
Seventy five patients with chronic idiopathic axonal polyneuropathy (CIAP) were studied for five years. The standardised and quantified neurological examination shows that progression of CIAP is slow, and handicap, if present, is not severe. During the follow up period a definite cause of the neuropathy was found in only four patients (two hereditary motor and sensory neuropathy type 2, one sensory chronic inflammatory demyelinating polyneuropathy, one alcoholic neuropathy). At the end of the follow up CIAP was not related to malignancy or gammopathy. Routine repetition of laboratory tests was not informative and these tests should be performed on clinical grounds only.
对75例慢性特发性轴索性多神经病(CIAP)患者进行了为期五年的研究。标准化和量化的神经学检查显示,CIAP进展缓慢,若存在功能障碍,也并不严重。在随访期间,仅在4例患者中发现了明确的神经病变病因(2例2型遗传性运动和感觉神经病、1例感觉性慢性炎症性脱髓鞘性多神经病、1例酒精性神经病)。随访结束时,CIAP与恶性肿瘤或丙种球蛋白病无关。常规重复实验室检查并无参考价值,这些检查仅应根据临床情况进行。