Journal of Pediatric Neurology 2015; 13(01): 008-010
DOI: 10.1055/s-0035-1555145
Review Article
Georg Thieme Verlag KG Stuttgart · New York

Pediatric Pseudotumor Cerebri Syndrome: Diagnostic Criteria and Classification

Claire A. Sheldon
1   Division of Ophthalmology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States
,
Grace L. Paley
1   Division of Ophthalmology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States
,
Shannon Beres
1   Division of Ophthalmology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States
,
Shana E. McCormack
2   Division of Endocrinology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States
,
Grant T. Liu
1   Division of Ophthalmology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States
› Author Affiliations
Further Information

Publication History

25 January 2015

30 January 2015

Publication Date:
13 July 2015 (online)

Abstract

Pseudotumor cerebri syndrome (PTCS) is defined by the presence of elevated intracranial pressure in the context of normal brain parenchyma and normal cytologic and chemical analyses of the cerebrospinal fluid. The presenting signs and symptoms of PTCS are various and usually include headache, papilledema, and visual disturbances (e.g., vision loss, double vision). Idiopathic intracranial hypertension, which is the primary form of PTCS, generally affects postpubertal overweight women of childbearing age. Secondary PTCS refers to a clinical diagnosis of PTCS attributable to one or more of a variety of identifiable causes, including venous sinus thrombosis, medications, and medical conditions other than obesity alone. The diverse clinical spectrum of pediatric PTCS is becoming increasingly recognized and recent research in this field is aiming to identify a common pathophysiology. We hereby review the recent diagnostic criteria and classification of pediatric PTCS.

 
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