Pseudotumor cerebri syndrome in children: Clinical characteristic and re-classification.

Children Freidman criteria Headache Idiopathic intracranial hypertension Jordan Papilledema Pseudotumor cerebri

Journal

Brain & development
ISSN: 1872-7131
Titre abrégé: Brain Dev
Pays: Netherlands
ID NLM: 7909235

Informations de publication

Date de publication:
Aug 2022
Historique:
received: 14 01 2022
revised: 14 03 2022
accepted: 22 03 2022
pubmed: 9 4 2022
medline: 1 6 2022
entrez: 8 4 2022
Statut: ppublish

Résumé

To describe the clinical characteristics of children with pseudotumor cerebri syndrome (PTCS) who were diagnosed according to the modified Dandy criteria and to reclassify them according to the newly proposed diagnostic criteria by Freidman. This retrospective study included the period from January 2016-to July 2021. 50 patients were included; 34 males and 16 females with a male to female ratio of 2.1:1. The average age at onset of symptoms was 8 years. Obesity was noticed in 6 (12%) patients; 34 (68%) had symptoms upon presentation. The most common presenting symptom was headache (28 patients; 56%), papilledema was present in 33 (66%) patients. Most patients (37; 74%) had an initial cerebrospinal fluid (CSF) pressure ≥280 mmH PTCS is a chronic condition. Managing patients who do not have papilledema or who do not meet the newly proposed higher CSF pressure is challenging. Although, applying the newly proposed criteria captured most of our patients, however, around one quarter were managed based on clinical experience. This study indicates a strong need for future guidelines tailored specifically for children, taking into consideration that the cut-off point of CSF pressure might not be similar for all populations.

Identifiants

pubmed: 35393129
pii: S0387-7604(22)00053-5
doi: 10.1016/j.braindev.2022.03.006
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

446-453

Informations de copyright

Copyright © 2022 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.

Auteurs

Amira Masri (A)

Department of Paediatrics,division of child neurology , Faculty of Medicine, The University of Jordan. Electronic address: masriamira69@hotmail.com.

Mira Al Jaberi (M)

Faculty of Medicine, The University of Jordan.

Raghad Shihadat (R)

Faculty of Medicine, The University of Jordan.

Abdallah Rayyan (A)

Faculty of Medicine, The University of Jordan.

Mohammad AlMasri (M)

Faculty of Medicine, The University of Jordan.

Lina Abuna'meh (L)

Department of Paediatrics,division of child neurology , Faculty of Medicine, The University of Jordan.

Majd Ali (M)

Department of Paediatrics,division of child neurology , Faculty of Medicine, The University of Jordan.

Nosaiba Al Ryalat (N)

Department of Radiology, Faculty of Medicine, The University of Jordan.

Azmy Hadidy (A)

Department of Radiology, Faculty of Medicine, The University of Jordan.

Ashjan Ahmad Al-Shakkah (AA)

Department of Radiology, Faculty of Medicine, The University of Jordan.

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Classifications MeSH