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Spontaneous resolution of a 13-mm Chiari malformation Type I in relation to differential growth of the posterior fossa volume.

Publication ,  Journal Article
Waldau, B; Domeshek, LF; Leigh, FA; Lum, KC; Fuchs, HE; Marcus, JR; Mukundan, S; Grant, GA
Published in: J Neurosurg Pediatr
February 2009

The case of a 3-year-old patient with tuberous sclerosis and a 13-mm Chiari malformation Type I that spontaneously disappeared over the course of 4 years is presented. Using morphometric measurements of the posterior fossa and cerebellum in this patient, the authors show that the volume of the posterior fossa at the time of initial evaluation was consistent with that reported as normal in the literature (180.24 cm3; normal volume 132-198 cm3). Moreover, the patient showed a normal rate of growth of his posterior fossa over the period of observation (201.05 cm3; normal range 153-230 cm3). Cerebellar volumes were found to increase only minimally during this time period, which is compatible with observations in healthy controls. The posterior fossa volume, on the other hand, was shown to increase significantly more than that of the cerebellum (p=0.0185). This differential growth may permit the tonsils to ascend back up into the posterior fossa. Therefore, pediatric patients with normal posterior fossa volumes and normal development may have a spontaneous resolution of their asymptomatic Chiari malformation Type I.

Duke Scholars

Published In

J Neurosurg Pediatr

DOI

ISSN

1933-0707

Publication Date

February 2009

Volume

3

Issue

2

Start / End Page

110 / 114

Location

United States

Related Subject Headings

  • Tuberous Sclerosis
  • Remission, Spontaneous
  • Organ Size
  • Neurology & Neurosurgery
  • Male
  • Magnetic Resonance Imaging
  • Humans
  • Follow-Up Studies
  • Cranial Fossa, Posterior
  • Child, Preschool
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Waldau, B., Domeshek, L. F., Leigh, F. A., Lum, K. C., Fuchs, H. E., Marcus, J. R., … Grant, G. A. (2009). Spontaneous resolution of a 13-mm Chiari malformation Type I in relation to differential growth of the posterior fossa volume. J Neurosurg Pediatr, 3(2), 110–114. https://doi.org/10.3171/2008.10.PEDS08200
Waldau, Ben, Leahthan F. Domeshek, Fawn A. Leigh, Kristian C. Lum, Herbert E. Fuchs, Jeffrey R. Marcus, Srinivasan Mukundan, and Gerald A. Grant. “Spontaneous resolution of a 13-mm Chiari malformation Type I in relation to differential growth of the posterior fossa volume.J Neurosurg Pediatr 3, no. 2 (February 2009): 110–14. https://doi.org/10.3171/2008.10.PEDS08200.
Waldau B, Domeshek LF, Leigh FA, Lum KC, Fuchs HE, Marcus JR, et al. Spontaneous resolution of a 13-mm Chiari malformation Type I in relation to differential growth of the posterior fossa volume. J Neurosurg Pediatr. 2009 Feb;3(2):110–4.
Waldau, Ben, et al. “Spontaneous resolution of a 13-mm Chiari malformation Type I in relation to differential growth of the posterior fossa volume.J Neurosurg Pediatr, vol. 3, no. 2, Feb. 2009, pp. 110–14. Pubmed, doi:10.3171/2008.10.PEDS08200.
Waldau B, Domeshek LF, Leigh FA, Lum KC, Fuchs HE, Marcus JR, Mukundan S, Grant GA. Spontaneous resolution of a 13-mm Chiari malformation Type I in relation to differential growth of the posterior fossa volume. J Neurosurg Pediatr. 2009 Feb;3(2):110–114.

Published In

J Neurosurg Pediatr

DOI

ISSN

1933-0707

Publication Date

February 2009

Volume

3

Issue

2

Start / End Page

110 / 114

Location

United States

Related Subject Headings

  • Tuberous Sclerosis
  • Remission, Spontaneous
  • Organ Size
  • Neurology & Neurosurgery
  • Male
  • Magnetic Resonance Imaging
  • Humans
  • Follow-Up Studies
  • Cranial Fossa, Posterior
  • Child, Preschool