Morphometric measurements of posterior cranial fossa and craniovertebral junction in Chiari I malformation with and without Syringohydromyelia

Authors

  • Pawitra Imemkamon Faculty of Medicine, Chulalongkorn University, King Chulalongkorn Memorial Hospital, Thai Red Cross Society, Bangkok, Thailand
  • Supada Prakkamakul Faculty of Medicine, Chulalongkorn University, King Chulalongkorn Memorial Hospital, Thai Red Cross Society, Bangkok, Thailand
  • Ketsuda Jakchairoongruang Faculty of Medicine, Chulalongkorn University, King Chulalongkorn Memorial Hospital, Thai Red Cross Society, Bangkok, Thailand

Keywords:

Chiari I, syringohydromyelia, measurement, craniocervical junction, posterior cranial fossa

Abstract

Background: Syringohydromyelia occurs about 30.0% - 85.0% in patients with Chiari I malformation (CMI). The syrinx formation is supposed to be a result of disturbed cerebrospinal fluid flow dynamics, which is associated with the degree of mechanical blockage that may be related to posterior cranial fossa (PCF) and craniovertebral junction anatomy.

Objective: Our study aimed to determine the morphometric difference in PCF and craniocervical junction between the CMI patients with and without syringohydromyelia.

Methods: Thirty CMI patients (16 with syringohydromyelia; 14 without syringohydromyelia) and 16 healthy subjects were also recruited. PCF and craniocervical junction measurements of 5 distances and 5 angles were performed. Comparison of these measurements was employed among the three groups.

Results: The clivus length and Klaus index in the CMI patients were shorter than in the controls (P = 0.002 and P < 0.001). The twining line was shorter in the CMI patients without syringohydromyelia when compared to the controls (P = 0.046). The Boogard’s and Nasion-basion-Opisthion (NBO) angles were larger, and the clivus gradient angle was smaller in the CMI patients with syringohydromyelia than the controls (P = 0.009, P = 0.014, and P = 0.009). Degree of tonsillar descent, the distances and the angles were not significantly different between the CMI patients with and without syringohydromelia.

Conclusion: Our study showed no difference in PCF and craniocervical junction morphometry between CMI patients with and without syringohydromyelia. The results support that CMI patients has underdeveloped PCF and more clivus horizontal orientation than the healthy subjects. Large population study with evaluation of mechanical and functional factors may help understanding and predicting the risk of syrinx formation among CMI individual.

Downloads

Download data is not yet available.

References

Caldarelli M, Di Rocco C. Diagnosis of Chiari I malformation and related syringomyelia: radiological and neurophysiological studies. Childs Nerv Syst 2004;20:332-5.https://doi.org/10.1007/s00381-003-0880-4

Milhorat TH, Chou MW, Trinidad EM, Kula RW, Mandell M, Wolpert C, et al. Chiari I malformation redefined: clinical and radiographic findings for 364 symptomatic patients. Neurosurgery 1999;44:1005-17.https://doi.org/10.1097/00006123-199905000-00042

Fernández AA, Guerrero AI, Martínez MI, Vázquez MA, Fernández JB, Chesa i Octavio E, et al. Malformations of the craniocervical junction (Chiari type I and syringomyelia: classification, diagnosis and treatment). BMC Musculoskeletal Disord 2009;10 Suppl 1:S1.

https://doi.org/10.1186/1471-2474-10-S1-S1

Bunck AC, Kroeger JR, Juettner A, Brentrup A, Fiedler B, Crelier GR, et al. Magnetic resonance 4D flow analysis of cerebrospinal fluid dynamics in Chiari I malformation with and without syringomyelia. Eur Radiol 2012;22:1860-70.

https://doi.org/10.1007/s00330-012-2457-7

Oldfield EH. Pathogenesis of Chiari I - pathophysiology of syringomyelia: implications for therapy: a summary of 3 decades of clinical research. Neurosurgery 2017; 64(CN_suppl_1):66-77.https://doi.org/10.1093/neuros/nyx377

Gad KA, Yousem DM. Syringohydromyelia in patients with Chiari I malformation: a retrospective analysis. AJNR Am J Neuroradiol 2017;38:1833-8.https://doi.org/10.3174/ajnr.A5290

Moore HE, Moore KR. Magnetic resonance imaging features of complex Chiari malformation variant of Chiari 1 malformation. Pediatr Radiol 2014;44:1403-11.https://doi.org/10.1007/s00247-014-3021-1

Alkoc OA, Songur A, Eser O, Toktas M, Gonul Y, Esi E, et al. Stereological and morphometric analysis of MRI Chiari malformation type-1. J Korean Neurosurg Soc 2015;58:454-61.https://doi.org/10.3340/jkns.2015.58.5.454

Houston JR, Eppelheimer MS, Pahlavian SH, Biswas D, Urbizu A, Martin BA, et al. A morphometric assessment of type I Chiari malformation above the McRae line: A retrospective case-control study in 302 adult female subjects. J Neuroradiol 2018;45:23-31.

https://doi.org/10.1016/j.neurad.2017.06.006

Furtado SV, Reddy K, Hegde AS. Posterior fossa morphometry in symptomatic pediatric and adult Chiari I malformation. J Clin Neurosci 2009;16:1449-54.https://doi.org/10.1016/j.jocn.2009.04.005

Karagoz F, Izgi N, Kapijcijoglu Sencer S. Morphometric measurements of the cranium in patients with Chiari type I malformation and comparison with the normal population. Acta Neurochir (Wien) 2002;144:165-71.

https://doi.org/10.1007/s007010200020

Furtado SV, Thakre DJ, Venkatesh PK, Reddy K, Hegde AS. Morphometric analysis of foramen magnum dimensions and intracranial volume in pediatric Chiari I malformation. Acta Neurochir 2010;152:221-7.https://doi.org/10.1007/s00701-009-0480-5

Urbizu A, Poca MA, Vidal X, Rovira A, Sahuquillo J, Macaya A. MRI-based morphometric analysis of posterior cranial fossa in the diagnosis of chiari malformation type I. J Neuroimaging 2014;24:250-6.https://doi.org/10.1111/jon.12007

Dufton JA, Habeeb SY, Heran MK, Mikulis DJ, Islam O. Posterior fossa measurements in patients with and without Chiari I malformation. Can J Neurol Sci 2011;38:452-5.https://doi.org/10.1017/S0317167100011860

Yan H, Han X, Jin M, Liu Z, Xie D, Sha S, et al. Morphometric features of posterior cranial fossa are different between Chiari I malformation with and without syringomyelia. Eur Spine J 2016;25:2202-9.https://doi.org/10.1007/s00586-016-4410-y

Schijman E. History, anatomic forms, and pathogenesis of Chiari I malformations. Childs Nerv Syst 2004;20:323-8.

https://doi.org/10.1007/s00381-003-0878-y

Stovner LJ, Bergan U, Nilsen G, Sjaastad O. Posterior cranial fossa dimensions in the Chiari I malformation: relation to pathogenesis and clinical presentation. Neuroradiology 1993;35:113-8.https://doi.org/10.1007/BF00593966

Elster AD, Chen MY. Chiari I malformations: clinical and radiologic reappraisal. Radiology 1992;183:347-53.

https://doi.org/10.1148/radiology.183.2.1561334

Nishikawa M, Sakamoto H, Hakuba A, Nakanishi N, Inoue Y. Pathogenesis of Chiari malformation: a morphometric study of the posterior cranial fossa. J Neurosurgery 1997;86:40-7.https://doi.org/10.3171/jns.1997.86.1.0040

Schady W, Metcalfe RA, Butler P. The incidence of craniocervical bony anomalies in the adult Chiari malformation. J Neurol Sci 1987;82:193-203.https://doi.org/10.1016/0022-510X(87)90018-9

Dagtekin A, Avci E, Kara E, Uzmansel D, Dagtekin O, Koseoglu A, et al. Posterior cranial fossa morphometry in symptomatic adult Chiari I malformation patients: comparative clinical and anatomical study. Clin Neurol Neurosur 2011;113:399-403.

https://doi.org/10.1016/j.clineuro.2010.12.020

Pinna G, Alessandrini F, Alfieri A, Rossi M, Bricolo A. Cerebrospinal fluid flow dynamics study in Chiari I malformation: implications for syrinx formation. Neurosurg Focus 2000;8:E3.https://doi.org/10.3171/foc.2000.8.3.3

Kennedy BC, Kelly KM, Anderson RC, Feldstein NA. Isolated thoracic syrinx in children with Chiari I malformation. Childs Nerv Syst 2016;32:531-4.https://doi.org/10.1007/s00381-015-3009-7

Downloads

Published

2023-07-18

How to Cite

1.
Imemkamon P, Prakkamakul S, Jakchairoongruang K. Morphometric measurements of posterior cranial fossa and craniovertebral junction in Chiari I malformation with and without Syringohydromyelia. Chula Med J [Internet]. 2023 Jul. 18 [cited 2024 Oct. 12];66(4). Available from: https://he05.tci-thaijo.org/index.php/CMJ/article/view/95