Your browser doesn't support javascript.
loading
Development of profound Chiari I malformation and cerebellar tissue loss and resolution following shunting of posterior fossa extra-axial cyst. Case report.
Khan, Rabia; Oakes, Peter; Tubbs, R Shane; Oakes, W Jerry.
Afiliación
  • Khan R; Seattle Science Foundation, 550 17th Avenue, James Tower, Suite 600, Seattle, WA, 98122, USA.
  • Oakes P; Seattle Science Foundation, 550 17th Avenue, James Tower, Suite 600, Seattle, WA, 98122, USA.
  • Tubbs RS; Seattle Science Foundation, 550 17th Avenue, James Tower, Suite 600, Seattle, WA, 98122, USA. shanet@seattlesciencefoundation.org.
  • Oakes WJ; Pediatric Neurosurgery, Children's of Alabama, Birmingham, AL, USA.
Childs Nerv Syst ; 33(1): 183-185, 2017 Jan.
Article en En | MEDLINE | ID: mdl-27444287
INTRODUCTION: Chiari I malformation can be due to a multitude of etiologies such as craniosynostosis or hydrocephalus. A posterior fossa extra-axial cyst (PFEAC) appears to be an extremely rare cause of this form of hindbrain herniation. CASE REPORT: Herein, we report a case of PFEAC that presented with no Chiari I malformation and then presented months later with a significant Chiari I malformation. Following shunt placement of a PFEAC, striking reversal of the Chiari malformation as well as reconstitution of the cerebellum was noted. CONCLUSIONS: Patients with PFEAC might develop a Chiari I malformation and this might be treated with shunting of the PFEAC alone.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Malformación de Arnold-Chiari / Encefalopatías / Quistes Tipo de estudio: Etiology_studies Límite: Child, preschool / Female / Humans Idioma: En Revista: Childs Nerv Syst Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Malformación de Arnold-Chiari / Encefalopatías / Quistes Tipo de estudio: Etiology_studies Límite: Child, preschool / Female / Humans Idioma: En Revista: Childs Nerv Syst Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos