Wulff C H, Hansen K, Strange P, Trojaborg W
J Neurol Neurosurg Psychiatry. 1983 Jun;46(6):485-90. doi: 10.1136/jnnp.46.6.485.
Four patients with Bannwarth's syndrome were examined. One to three weeks weeks after the appearance of a large erythematous skin lesion they developed pain of variable localisation. Four days to four weeks later uni- or bilateral facial palsies and other nerve lesions developed. CSF showed elevated protein and mononuclear pleocytosis. There was a defect of the blood-brain barrier and increased intrathecal production of IgG. Facial nerve latencies were increased 4 to 7 times in three cases and normal in one case examined 15 months after onset. Conduction velocity along other nerves was normal apart from slight slowing in one diabetic patient. Recovery was incomplete in three patients 8 to 15 months after onset of disease and complete in one patient after 15 months.
对4例巴恩沃思综合征患者进行了检查。在出现大片红斑性皮肤损害1至3周后，他们出现了部位不一的疼痛。4天至4周后，出现单侧或双侧面瘫及其他神经病变。脑脊液显示蛋白升高和单核细胞增多。存在血脑屏障缺陷和鞘内IgG产生增加。3例患者面神经潜伏期增加了4至7倍，1例在发病15个月后检查时潜伏期正常。除1例糖尿病患者传导速度略有减慢外，其他神经的传导速度正常。3例患者在发病8至15个月后恢复不完全，1例患者在15个月后完全恢复。
