Massimi L, Novegno F, di Rocco C
Pediatric Neurosurgery, Catholic University Medical School, Rome, Italy.
Adv Tech Stand Neurosurg. 2011(37):143-211. doi: 10.1007/978-3-7091-0673-0_6.
The diagnosis of Chiari type I malformation (CIM) is more and more frequent in clinical practice due to the wide diffusion of magnetic resonance imaging. In many cases, such a diagnosis is made incidentally in asymptomatic patients, as including children investigated for different reasons such as mental development delay or sequelae of brain injury. The large number of affected patients, the presence of asymptomatic subjects, the uncertainties surrounding the pathogenesis of the malformation, and the different options for its surgical treatment make the management of CIM particularly controversial.This paper reports on the state of the art and the recent achievements about CIM aiming at providing further information especially on the pathogenesis, the natural history, and the management of the malformation, which are the most controversial aspects. A historial review introduces and explains the current classification. Furthermore, the main clinical, radiological, and neurophysiological findings of CIM are described to complete the picture of this heterogeneous and complex disease.
由于磁共振成像的广泛应用,Chiari I型畸形(CIM)在临床实践中的诊断越来越频繁。在许多情况下,这种诊断是在无症状患者中偶然做出的,包括因不同原因(如智力发育迟缓或脑损伤后遗症)接受检查的儿童。大量受影响的患者、无症状受试者的存在、围绕畸形发病机制的不确定性以及其手术治疗的不同选择,使得CIM的管理极具争议性。本文报道了CIM的最新进展和近期成果,旨在提供更多信息,特别是关于畸形的发病机制、自然史和管理,这些是最具争议的方面。历史回顾介绍并解释了当前的分类。此外,还描述了CIM的主要临床、放射学和神经生理学发现,以完善这种异质性和复杂性疾病的全貌。