Berger Joseph R, Espinosa Patricio S, Kissel John
Department of Neurology, University of Kentucky College of Medicine, Lexington, KY 40536-0284, USA.
Arch Neurol. 2005 May;62(5):817-23. doi: 10.1001/archneur.62.5.817.
Although amyotrophic lateral sclerosis and progressive spinal muscular atrophy have been recognized to occur in association with human immunodeficiency virus infection, to our knowledge, brachial amyotrophic diplegia, a form of segmental motor neuron disease, has not been previously reported. Brachial amyotrophic diplegia results in severe lower motor neuron weakness and atrophy of the upper extremities in the absence of bulbar or lower extremity involvement, pyramidal features, bowel and bladder incontinence, and sensory loss. We describe a human immunodeficiency virus-seropositive man without severe immunosuppression or prior AIDS-defining illnesses who had brachial amyotrophic diplegia. This disorder may represent one end of a spectrum of motor neuron diseases occurring with this retrovirus infection.
虽然肌萎缩侧索硬化症和进行性脊髓性肌萎缩症已被认为与人类免疫缺陷病毒感染有关,但据我们所知,节段性运动神经元病的一种形式——臂丛性肌萎缩性双侧瘫,此前尚未见报道。臂丛性肌萎缩性双侧瘫会导致严重的下运动神经元无力以及上肢萎缩,而无延髓或下肢受累、锥体束征、大小便失禁及感觉丧失。我们描述了一名人类免疫缺陷病毒血清反应阳性的男性,他没有严重免疫抑制或先前的艾滋病界定疾病,却患有臂丛性肌萎缩性双侧瘫。这种病症可能代表了这种逆转录病毒感染所引发的一系列运动神经元疾病的一端。