Oishi M, Mori N, Takasu T, Osaka S, Yamamoto M, Uchiyama T, Sawada S
Department of Neurology, Nihon University School of Medicine, Japan.
Acta Neurol (Napoli). 1993 Feb;15(1):53-61.
A case of Nasu-Hakola disease (membranous lipodystrophy) was reported. The patient is a 33-year-old man who started to have pathological fractures at the age of 24 years. Then, neurological symptoms such as dementia appeared gradually. A biopsy specimen of the bone showed membranocystic changes of the adipose tissue. T2-weighted magnetic resonance images of the head showed low intensity in bilateral putamens, internal capsules, globi pallidi and caudate nuclei. One of his brothers has the same disease. In both patients, fatty acid composition of serum total lipids showed increased nervonic acid and plasma amino acid analysis showed decreased glutamine.
报告了一例纳苏-哈科拉病(膜性脂肪营养不良)。患者为一名33岁男性,24岁时开始出现病理性骨折。随后,逐渐出现痴呆等神经症状。骨活检标本显示脂肪组织呈膜性囊肿样改变。头部的T2加权磁共振图像显示双侧壳核、内囊、苍白球和尾状核呈低信号。他的一个兄弟患有同样的疾病。在这两名患者中,血清总脂质的脂肪酸组成显示神经酸增加,血浆氨基酸分析显示谷氨酰胺减少。