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检测与教学。病例七十三。诊断:亚历山大病。

Test and teach. Number seventy-three. Diagnosis: Alexander's disease.

作者信息

Moore L, Bourne A J, Byard R W

机构信息

Department of Histopathology, Women's and Children's Hospital, North Adelaide, South Australia.

出版信息

Pathology. 1993 Jul;25(3):254, 321. doi: 10.3109/00313029309066585.

Abstract

Alexander's disease is a progressive degenerative neurological disorder developing in early childhood which is characterized by accumulation of Rosenthal fibres throughout the cerebral white matter. These fibres are composed of glial fibrillary acidic protein and ubiquinated alpha beta crystallin. The absence of atypia, increased cellularity, mitotic activity or necrosis in biopsy material allows differentiation from neoplasia glial processes. Clinical features suggestive of the diagnosis include progressive mental retardation with an increase in head circumference.

摘要

亚历山大病是一种在儿童早期发病的进行性退行性神经疾病,其特征是整个脑白质中出现罗森塔尔纤维堆积。这些纤维由胶质纤维酸性蛋白和泛素化的αβ晶状体蛋白组成。活检材料中不存在异型性、细胞增多、有丝分裂活性或坏死,这有助于与神经胶质细胞瘤相鉴别。提示该诊断的临床特征包括进行性智力发育迟缓伴头围增大。

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