Abstract
While normal-pressure hydrocephalus (NPH) is most commonly diagnosed in older adulthood, a significant body of literature has accumulated over half a century documenting the clinical phenomenon of an NPH-like syndrome in pediatric patients. As in adult NPH, it is likely that pediatric NPH occurs due to a heterogeneous array of developmental, structural, and neurodegenerative pathologies, ultimately resulting in aberrant cerebrospinal fluid (CSF) flow and distribution within and around the brain. In this review, we aimed to systematically survey the existing clinical evidence supporting the existence of a pediatric form of NPH, dating back to the original recognition of NPH as a clinically significant subtype of communicating hydrocephalus. Leveraging emergent trends from the old and more recent published literature, we then present a modern characterization of pediatric NPH as a disorder firmly within the same disease spectrum as adult NPH, likely with overlapping etiology and pathophysiological mechanisms. Exemplary cases consistent with the diagnosis of pediatric NPH selected from the senior author’s neurosurgical practice are then presented alongside the systematic review to aid in discussion of the typical clinical and radiographic manifestations of pediatric NPH. Common co-morbidities and modern surgical treatment options are also described.
Highlights
Among 16 patients < 20 years in age presenting with normal-pressure hydrocephalus (NPH), most displayed elements of the diagnostic triad, and intracranial pressure (ICP) was found to be within normal limits for 6/6 patients tested; shunting produced symptomatic improvement in 12/16
Consistent with prior hypotheses about disordered cerebrospinal fluid (CSF) production, recent reports and limited series have emerged highlighting specific genetic mutations which may be associated with the development of NPH early in life, in particular genes related to cilia motility [1,3]
Normal-pressure hydrocephalus (NPH) remains a pertinent clinical diagnosis which is likely heterogeneous in pathophysiology and can occur in patients across the life cycle, including both older adults and children
Summary
In the adult or aging population, NPH is classified as “idiopathic NPH”
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