Dyke-Davidoff-Masson syndrome in an 8-year-old child: Report of a case.
Calvarial thickening
Children
Dyke-Davidoff-Masson syndrome
Epileptic seizures
Hemi cerebral atrophy
MRI
Journal
Radiology case reports
ISSN: 1930-0433
Titre abrégé: Radiol Case Rep
Pays: Netherlands
ID NLM: 101467888
Informations de publication
Date de publication:
Jan 2024
Jan 2024
Historique:
received:
01
07
2023
revised:
29
09
2023
accepted:
30
09
2023
medline:
29
11
2023
pubmed:
29
11
2023
entrez:
29
11
2023
Statut:
epublish
Résumé
Dyke-Davidoff-Masson syndrome (DDMS) is a rare entity. Few cases have been described in the literature. It can be symptomatic or asymptomatic. The clinical signs are very varied. Imaging is the key to diagnosis. Calvarial thickening, enlargement sinus, and cerebral hemiatrophy are suggestive signs. It is a cause of cerebral hemiatrophy and epilepsy. We report the clinical and radiological signs of this syndrome through a case of an 8-year-old male child treated for epilepsy. The importance of our article is to report a case diagnosed at an early age (8 years). Most studies report cases diagnosed in adults. MRI revealed pathognomonic signs of Dyke-Davidoff-Masson syndrome.
Identifiants
pubmed: 38028307
doi: 10.1016/j.radcr.2023.09.106
pii: S1930-0433(23)00741-0
pmc: PMC10630757
doi:
Types de publication
Case Reports
Langues
eng
Pagination
239-241Informations de copyright
© 2023 The Authors. Published by Elsevier Inc. on behalf of University of Washington.
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