Fukutake T, Hirayama K
Department of Neurology, Chiba University School of Medicine, Japan.
Eur Neurol. 1995;35(2):69-79. doi: 10.1159/000117096.
Here we review a total of 17 patients, including 4 of our own, with young-adult-onset arteriosclerotic leukoencephalopathy, alopecia and lumbago without hypertension. All were Japanese and the illness seemed to be transmitted in an autosomal recessive fashion. The male to female ratio was 7.5:1. The age of onset usually ranged from 25 to 30 years. Acute lumbago, spondylosis deformans, diffuse baldness, and progressive motor and mental deterioration were common clinical features. Cerebral arteriosclerosis and white mater disease were demonstrated pathologically or radiologically. Although the pathogenesis has remained obscure, we think this is a new clinico-pathological entity distinct from the classic type of Binswanger's disease.
我们在此回顾了总共17例患有青年期起病的动脉硬化性白质脑病、脱发和腰痛且无高血压的患者,其中包括我们自己的4例患者。所有患者均为日本人,且该疾病似乎以常染色体隐性方式遗传。男女比例为7.5:1。发病年龄通常在25岁至30岁之间。急性腰痛、脊柱变形、弥漫性脱发以及进行性运动和精神衰退是常见的临床特征。通过病理或放射学检查证实存在脑动脉硬化和白质疾病。尽管发病机制仍不清楚,但我们认为这是一种不同于经典型宾斯旺格病的新的临床病理实体。