Surgical outcomes of calvaria reconstruction in cranial pansynostosis associated with Arnold‐Chiari type 1.5 malformation, a case report

A 6‐year‐old girl with persistent headaches and the visual problem was diagnosed as a delayed onset cranial pansynostosis with concurrent type 1.5 Arnold‐Chiari malformation. She underwent multi‐sutural reconstructive surgery and followed. The headache was greatly decreased and tonsillar‐brain stem...

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Detalles Bibliográficos
Autores principales: Tabesh, Homayoun, Riazi, Ali, Mahmoodkhani, Mehdi, Sharafi, Mohammad, Sourani, Arman, Mahdkhah, Ata, Foroughi, Mina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986723/
https://www.ncbi.nlm.nih.gov/pubmed/36891239
http://dx.doi.org/10.1002/ccr3.6981
Descripción
Sumario:A 6‐year‐old girl with persistent headaches and the visual problem was diagnosed as a delayed onset cranial pansynostosis with concurrent type 1.5 Arnold‐Chiari malformation. She underwent multi‐sutural reconstructive surgery and followed. The headache was greatly decreased and tonsillar‐brain stem herniation and syrinx were resolved.

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