A Rare Case of Infantile Myofibromatosis With Intra Cranial Involvement.
computed tomography
infantile myofibromatosis
intracranial
magnetic resonance imaging
pediatric tumor
Journal
Global pediatric health
ISSN: 2333-794X
Titre abrégé: Glob Pediatr Health
Pays: United States
ID NLM: 101670224
Informations de publication
Date de publication:
2024
2024
Historique:
received:
19
01
2024
revised:
07
06
2024
accepted:
12
06
2024
medline:
19
8
2024
pubmed:
19
8
2024
entrez:
19
8
2024
Statut:
epublish
Résumé
Infantile myofibromatosis is a proliferative disorder occurring during infancy and early childhood, marked by the development of nodular or diffuse lesions consisting of various mesenchymal elements. Intracranial involvement is infrequently reported. Here, we present the case of a 3-year-old girl exhibiting a rare manifestation of IM with intracranial parenchymal involvement, displaying a histological pattern documented in existing literature on patients with infantile myofibromatosis. Subsequent MRI follow-up revealed no signs of recurrence.
Identifiants
pubmed: 39157296
doi: 10.1177/2333794X241266564
pii: 10.1177_2333794X241266564
pmc: PMC11329903
doi:
Types de publication
Case Reports
Journal Article
Langues
eng
Pagination
2333794X241266564Informations de copyright
© The Author(s) 2024.
Déclaration de conflit d'intérêts
The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.