Nishimura R N, Ishak K G, Reddick R, Porter R, James S, Barranger J A
Ann Neurol. 1980 Oct;8(4):409-15. doi: 10.1002/ana.410080412.
We have studied four patients who had a clinical course compatible with Lafora disease. The diagnosis was confirmed in one by the presence of Lafora bodies in central nervous system neurons at autopsy and was supported in another by findings in the cerebral biopsy of a sibling. Our patients had no clinically apparent liver disease, but liver specimens in each instance showed a distinctive histological abnormality, with hepatocytes containing inclusions having a ground-glass appearance. The liver biopsy findings appear to be relatively specific for this disorder and can easily be differentiated from those in other liver diseases.
我们研究了4例临床病程符合拉福拉病的患者。其中1例经尸检发现中枢神经系统神经元中有拉福拉小体而确诊,另1例则因同胞的脑活检结果而得到支持。我们的患者临床上无明显肝脏疾病,但每例患者的肝脏标本均显示出一种独特的组织学异常,肝细胞内含有具有毛玻璃样外观的包涵体。肝活检结果似乎对此病具有相对特异性,且很容易与其他肝脏疾病的结果相区分。