deSouza N, Chaudhuri R, Bingham J, Cox T
Department of Magnetic Resonance, Guys' Hospital, London, UK.
Neuroradiology. 1994;36(2):148-51. doi: 10.1007/BF00588085.
Cerebellar hypoplasia may present with a wide variety of neurological and systemic features, ranging from aplasia causing neonatal death to mild hypoplasia in an asymptomatic adult. MRI clearly documents the size of the cerebellum and any associated abnormalities. We describe 7 cases of cerebellar hypoplasia of varying aetiology--3 inherited, 2 associated with spinal dysraphism, 1 with Joubert's syndrome and 1 with pontine agenesis, probably as a result of basilar artery infarction in utero. T1- and T2-weighted images were obtained in each case and gadolinium-DTPA was administered in one. Associated features such as a Chiari malformation (2 cases), brain stem hypoplasia (2 cases), Dandy-Walker cyst and pachygyria (3 cases) and spinal dysraphism (2 cases) were clearly identified. Accurate documentation of these appearances assists in genetic counselling.
小脑发育不全可能呈现出各种各样的神经和全身特征,范围从导致新生儿死亡的发育不全到无症状成年人的轻度发育不全。磁共振成像(MRI)能清晰记录小脑的大小及任何相关异常。我们描述了7例病因各异的小脑发育不全病例——3例为遗传性,2例与脊柱裂相关,1例与朱伯特综合征相关,1例与脑桥发育不全相关,后者可能是由于子宫内基底动脉梗死所致。对每个病例均获取了T1加权和T2加权图像,其中1例使用了钆喷酸葡胺。明确识别出了相关特征,如Chiari畸形(2例)、脑干发育不全(2例)、Dandy-Walker囊肿和巨脑回(3例)以及脊柱裂(2例)。准确记录这些表现有助于进行遗传咨询。