Soto-Ares G, Delmaire C, Deries B, Vallee L, Pruvo J P
Department of Neuroradiology, Hôpital Roger Salengro, Chru Lille France.
AJNR Am J Neuroradiol. 2000 Sep;21(8):1511-9.
MR imaging findings of cerebellar cortical dysplasia have been described as a new cerebellar malformation. The purpose of this study was to assess the association of cerebellar cortical dysplasia with other cerebral malformations.
We retrospectively reviewed 46 MR examinations of patients presenting with developmental delay, hypotonia, and facial deformities to identify abnormal folia or fissures or both within cerebellar hemispheres or vermis suggesting cortical dysplasia.
Cerebellar cortical dysplasia was diagnosed in 17 patients. In two patients, it was isolated. In the remaining 15 patients, the malformation was associated with vermian malformation (n=11), cerebral cortical dysplasias (n=8), dysplasia of corpus callosum (n=6), and heterotopia (n=5). A widespread malformation of the posterior fossa was observed in eight patients (Dandy-Walker, Chiari II and III, and hypoplasia of brain stem). One patient with hypertrophied cerebellar hemisphere had minor enlargement of the right cerebral hemisphere and lateral ventricle. He also had nodular heterotopia, suggesting unilateral megalencephaly.
Our study suggests that cerebellar cortical dysplasias are common in cases with more widespread cerebral malformations. Technical progress providing high-quality tridimensional MR imaging of the cerebellum may explain its recent descriptions.
小脑皮质发育异常的磁共振成像表现已被描述为一种新的小脑畸形。本研究的目的是评估小脑皮质发育异常与其他脑畸形的关联。
我们回顾性分析了46例发育迟缓、肌张力减退和面部畸形患者的磁共振检查,以确定小脑半球或蚓部内提示皮质发育异常的异常小叶或裂隙或两者皆有。
17例患者被诊断为小脑皮质发育异常。其中2例为孤立性病变。其余15例患者中,该畸形与蚓部畸形(n = 11)、大脑皮质发育异常(n = 8)、胼胝体发育异常(n = 6)和异位(n = 5)相关。8例患者观察到广泛的后颅窝畸形(丹迪-沃克畸形、Chiari II和III型以及脑干发育不全)。1例小脑半球肥大患者右侧大脑半球和侧脑室轻度增大。他还患有结节性异位,提示单侧巨脑症。
我们的研究表明,小脑皮质发育异常在更广泛的脑畸形病例中很常见。提供高质量小脑三维磁共振成像的技术进步可能解释了其最近才被描述的原因。