UO Neurologia dello Sviluppo, Fondazione IRCCS Istituto Neurologico C. Besta, Via Celoria 11, 20133, Milan, Italy.
Neurol Sci. 2011 Dec;32 Suppl 3:S295-8. doi: 10.1007/s10072-011-0744-8.
The clinical features of Chiari I Malformation (CIM) may be related to the compression of dural and/or neural structures at the craniocervical junction or to the associated syringomyelia. Additionally, patients may exhibit symptoms and signs of associated disorders. CIM is a heterogeneous and multifactorial disorder including congenital and acquired forms; it can also be found as an isolated malformation or in association with many clinical conditions. We analyse the clinical features in a series of 65 children with CIM, focusing on the high frequency of associated clinical disorders. We emphasise the importance of a careful clinical and neurological assessment for a proper diagnosis and a correct management of these patients.
Chiari I 畸形(CIM)的临床特征可能与颅颈交界区硬脑膜和/或神经结构的受压有关,或与相关的脊髓空洞症有关。此外,患者可能表现出相关疾病的症状和体征。CIM 是一种异质性和多因素的疾病,包括先天性和获得性;它也可以作为一种孤立的畸形存在,或与许多临床情况有关。我们分析了 65 例 CIM 患儿的临床特征,重点关注相关临床疾病的高频率。我们强调了仔细的临床和神经学评估对于正确诊断和治疗这些患者的重要性。