Mizuguchi M, Maekawa S, Kamoshita S
Department of Pediatrics, Faculty of Medicine, University of Tokyo, Japan.
Arch Neurol. 1994 Sep;51(9):951-4. doi: 10.1001/archneur.1994.00540210125022.
To clarify the pathogenetic significance of the topographic distribution of leptomeningeal glioneuronal heterotopia, a common finding in holoprosencephaly.
Gross, histological, and immunohistochemical observations of alobar holoprosencephaly in brain specimens taken at autopsy.
Referral center.
Brains removed at autopsy from five consecutive patients with alobar holoprosencephaly.
Immunoperoxidase staining for glial fibrillary acidic protein.
In all brains, leptomeningeal glioneuronal heterotopia showed an identical distribution, ranging from the basal prosencephalon to the pons, with the thickest distribution occurring in the basal prosencephalon.
The constant localization implicates leptomeningeal glioneuronal heterotopia in severe dysgenesis of midline prosencephalon, the basic pathogenesis of the anomaly.
明确软脑膜神经胶质神经元异位的局部分布在全前脑畸形中的致病意义,全前脑畸形中常见此表现。
对尸检获取的脑标本中无脑叶型全前脑畸形进行大体、组织学及免疫组化观察。
转诊中心。
连续5例无脑叶型全前脑畸形患者尸检取出的脑。
胶质纤维酸性蛋白免疫过氧化物酶染色。
在所有脑标本中,软脑膜神经胶质神经元异位分布相同,从基底前脑延伸至脑桥,基底前脑处分布最厚。
这种恒定的定位表明软脑膜神经胶质神经元异位与中线前脑的严重发育异常有关,这是该畸形的基本发病机制。