Radiologic evaluation of pediatric hydrocephalus

• Published in: Child's nervous system 2011-10, Vol.27 (10), p.1543-1562
• Main Authors: Dincer, Alp, Ozek, M Memet
• Format: Article
• Language: English
• Subjects: Diagnostic Imaging; Humans; Hydrocephalus - diagnosis; Imaging, Three-Dimensional; Medicine; Medicine & Public Health; Neurosciences; Neurosurgery; Pediatrics; Special Annual Issue; Ultrasonography
• ISSN: 0256-7040; 1433-0350
• DOI: 10.1007/s00381-011-1559-x

Introduction The aim of this review is to present the contemporary role of radiology in evaluating pediatric hydrocephalus. Although conventional brain imaging with ultrasound (US), computed tomography (CT), and magnetic resonance imaging (MRI) reveal the degree of ventricular enlargement and often the etiology of the hydrocephalus, the diagnosis and management of hydrocephalus present common problems in pediatric populations. Discussion US, usually sufficient to assess and monitor ventricular size, is used most commonly in preterm infants who have germinal matrix hemorrhages and not able to tolerate transport to the radiology department. Although CT can demonstrate gross dilatation of ventricles, in most cases, it will be necessary to more closely define the nature of the obstruction, either functionally or anatomically. MRI is the best imaging modality to provide such functional and anatomic information. However, since identification of obstructive pathologic processes at any level through the cerebrospinal fluid (CSF) pathway in patients with hydrocephalus is of significant importance because it can change the treatment options, avoiding shunt insertion, a more sophisticated MRI approach is needed instead of obtaining a routine cranial MRI. Furthermore, the outcome after neuroendoscopic procedures is clearly related to patient selection under guidance of neuroimaging. Conclusion Therefore, the article focuses mainly on the effective usage of various MRI sequences in both diagnosis and follow-up of pediatric hydrocephalus, such as 3D CISS, cine PC, TSE, and GRE T2* sequences, to be able to investigate all possible obstructive pathology through the CSF pathway and to assess the efficiency of treatment in a standardized way.