Passarin M G, Salviati A, Gambina G, Tezzon F, Tomelleri G, Deotto L, Zanoni T, Bovi P, Gerosa M, Nicolato A, Mazza C, Iuzzolino P, Ghimenton C, Ferrari G
Divisione di Neurologia, Ospedale Maggiore, Università di Verona, Italy.
Ital J Neurol Sci. 1996 Aug;17(4):295-300. doi: 10.1007/BF01997790.
Three members of the same family were studied, all of whom had multiple intracerebral cavernous angiomas for which a dominant autosomal inheritance was hypothesised. The proband suffered from headaches, and physical examination revealed evident right hemiparesis. The second case started with a hemorrhagic cerebral stroke and the third was asymptomatic on neurological examination. Nuclear magnetic resonance (NMR), performed in two of the three cases, showed lesions whose number and extent were not radiologically characteristic of cavernous angioma. A cerebral biopsy of the proband enabled the diagnosis to be made. Despite the recent introduction of NMR, the nosological classification of familial forms can be difficult when the radiological lesions are atypical. In such cases, cerebral biopsy is not only a valid diagnostic aid, but is also indispensable for obtaining adequate genetic information.
对同一家族的三名成员进行了研究,他们都患有多发性脑内海绵状血管瘤,推测为常染色体显性遗传。先证者患有头痛,体格检查发现明显的右侧偏瘫。第二例以出血性脑卒中来诊,第三例经神经学检查无症状。在三例中的两例进行了核磁共振(NMR)检查,显示出的病变在数量和范围上并非海绵状血管瘤的典型放射学特征。对先证者进行脑活检得以确诊。尽管最近引入了核磁共振检查,但当放射学病变不典型时,家族性类型的疾病分类可能会很困难。在这种情况下,脑活检不仅是一种有效的诊断辅助手段,而且对于获取足够的基因信息也是必不可少的。