Lange D J, Britton C B, Younger D S, Hays A P
Department of Neurology, College of Physicians and Surgeons, Columbia University, New York, NY.
Arch Neurol. 1988 Oct;45(10):1084-8. doi: 10.1001/archneur.1988.00520340038008.
We studied 14 patients with neuromuscular disorders and concomitant infection with human immunodeficiency virus to define clinical syndromes and prognosis. Eight patients had painful sensorimotor peripheral neuropathy; two, chronic inflammatory demyelinating polyneuropathy; two, mononeuropathy or mononeuropathy multiplex; one, recurrent myoglobinuria; and one, chronic proximal weakness and elevated creatine kinase levels. All eight patients with painful neuropathy had overt symptoms of acquired immunodeficiency syndrome. Chronic inflammatory demyelinating polyneuropathy was the first manifestation of acquired immunodeficiency syndrome in both patients with this syndrome. Both died from overwhelming sepsis within six months of the neuropathy's onset. Patients with mononeuropathy multiplex had a variable course. Immunosuppressant medication had no effect in two patients.
我们研究了14例患有神经肌肉疾病并合并感染人类免疫缺陷病毒的患者,以确定临床综合征和预后情况。8例患者患有疼痛性感觉运动性周围神经病;2例患有慢性炎症性脱髓鞘性多发性神经病;2例患有单神经病或多灶性单神经病;1例患有复发性肌红蛋白尿;1例患有慢性近端肌无力且肌酸激酶水平升高。所有8例患有疼痛性神经病的患者均有获得性免疫缺陷综合征的明显症状。慢性炎症性脱髓鞘性多发性神经病是这2例患有该综合征患者获得性免疫缺陷综合征的首发表现。两人均在神经病发作后6个月内死于严重败血症。多灶性单神经病患者的病程各不相同。免疫抑制药物对2例患者无效。