Chiari type I malformations in adults: a morphometric analysis of the posterior cranial fossa

2005 ◽  
Vol 64 (3) ◽  
pp. 237-241 ◽  
Author(s):  
Sabri Aydin ◽  
Hakan Hanimoglu ◽  
Taner Tanriverdi ◽  
Ercument Yentur ◽  
Mehmet Yasar Kaynar
2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Ümit Erkan Vurdem ◽  
Niyazi Acer ◽  
Tolga Ertekin ◽  
Ahmet Savranlar ◽  
Mehmet Fatih İnci

Objective. The aim of this study was to determine the posterior cranial fossa volume, cerebellar volume, and herniated tonsillar volume in patients with chiari type I malformation and control subjects using stereological methods.Material and Methods. These volumes were estimated retrospectively using the Cavalieri principle as a point-counting technique. We used magnetic resonance images taken from 25 control subjects and 30 patients with chiari type I malformation.Results. The posterior cranial fossa volume in patients with chiari type I malformation was significantly smaller than the volume in the control subjects (P<0.05). In the chiari type I malformation group, the cerebellar volume was smaller than the control group, but this difference was not statistically significant (P>0.05). In the chiari type I malformation group, the ratio of cerebellar volume to posterior cranial fossa volume was higher than in the control group. We also found a positive correlation between the posterior cranial fossa volume and cerebellar volume for each of the groups (r=0.865,P<0.001). The mean (±SD) herniated tonsillar volume and length were0.89±0.50 cm3and9.63±3.37 mm in the chiari type I malformation group, respectively.Conclusion. This study has shown that posterior cranial fossa and cerebellum volumes can be measured by stereological methods, and the ratio of these measurements can contribute to the evaluation of chiari type I malformation cases.


2013 ◽  
Vol 78 (1) ◽  
pp. 1-12 ◽  
Author(s):  
Christina A. Markunas ◽  
David S. Enterline ◽  
Kaitlyn Dunlap ◽  
Karen Soldano ◽  
Heidi Cope ◽  
...  

2013 ◽  
Vol 24 (3) ◽  
pp. 250-256 ◽  
Author(s):  
Aintzane Urbizu ◽  
Maria-Antonia Poca ◽  
Xavier Vidal ◽  
Alex Rovira ◽  
Juan Sahuquillo ◽  
...  

2018 ◽  
Vol 12 ◽  
Author(s):  
Maggie S. Eppelheimer ◽  
James R. Houston ◽  
Jayapalli R. Bapuraj ◽  
Richard Labuda ◽  
Dorothy M. Loth ◽  
...  

2011 ◽  
Vol 31 (3) ◽  
pp. E3 ◽  
Author(s):  
Marios Loukas ◽  
Brian J. Shayota ◽  
Kim Oelhafen ◽  
Joseph H. Miller ◽  
Joshua J. Chern ◽  
...  

A single pathophysiological mechanism of Chiari Type I malformations (CM-I) has been a topic of debate. To help better understand CM-I, the authors review disorders known to be associated with CM-I. The primary methodology found among most of them is deformation of the posterior cranial fossa, usually with subsequent decrease in volume. Other mechanisms exist as well, which can be categorized as either congenital or acquired. In understanding the relationship of such disorders with CM-I, we may gain further insight into the process by which cerebellar tonsillar herniation occurs. Some of these pathologies appear to be true associations, but many appear to be spurious.


2011 ◽  
Vol 27 (10) ◽  
pp. 1653-1664 ◽  
Author(s):  
Concezio Di Rocco ◽  
Paolo Frassanito ◽  
Luca Massimi ◽  
Simone Peraio

2000 ◽  
Vol 47 (12) ◽  
pp. 1220-1223 ◽  
Author(s):  
Daryl L. Williams ◽  
Hamed Umedaly ◽  
I. Lynn Martin ◽  
Anthony Boulton

Author(s):  
Abdulhamid Ciçek ◽  
Jeroen Cortier ◽  
Sarah Hendrickx ◽  
Johan Van Cauwenbergh ◽  
Lien Calus ◽  
...  

Abstract Introduction Chiari type I malformations can present in different ways, but the most frequent symptom is an occipitocervical headache. Hearing loss as the main presenting symptom is rare. Case A young woman with progressive left-sided unilateral hearing loss was diagnosed with a Chiari type I malformation. She underwent a suboccipital craniectomy with C1 laminectomy and duraplasty. The hearing loss had resolved postoperatively with normalization of the audiometry. Conclusion Chiari type I malformation can present solely with hearing loss. Improvement after surgical decompression is possible. This phenomenon is not emphasized well enough within the neurologic community. In this report, we present a summary of the pathophysiology and management in Chiari type I malformations.


OBJECTIVE Posterior vault distraction osteogenesis (PVDO) is an effective tool to increase intracranial volume and expand the posterior cranial fossa. During PVDO, the authors extended osteotomy posterior to the foramen magnum to fully expand the posterior cranial fossa. The aim of this study was to investigate the efficacy of complete PVDO in posterior fossa expansion and treatment of Chiari malformation type I (CM-I) in patients with craniosynostosis. METHODS Patients with craniosynostosis who had undergone complete PVDO between January 2012 and May 2020 were reviewed retrospectively. A coronal osteotomy extending to the foramen magnum was performed and the foramen magnum was decompressed by removing its posterior rim with a 1-mm Kerrison rongeur. Four distractor devices were placed and the vector of distraction was controlled from the posterior to the inferior-posterior direction, depending on the deformity. Changes in the intracranial volume, posterior cranial fossa area, and cerebellar tonsillar descent were measured after complete PVDO by using CT and MRI. RESULTS A total of 11 patients with craniosynostosis and concurrent CM-I were included in the study. The mean age was 34.6 ± 24.0 months (continuous variables are expressed as the mean ± SD throughout). One patient had sleep apnea, which was consistent with CM-I, and another patient had a headache, which was nonspecific. The intracranial volume increased from 1179.6 ± 180.2 cm3 to 1440.6 ± 251.5 cm3 (p = 0.003; 24.5% increase compared to the preoperative volume). The posterior skull base area increased from 44.9 ± 19.3 cm2 to 72.7 ± 18.1 cm2 (p = 0.004). Cerebellar tonsillar descent decreased in all 11 patients after complete PVDO (preoperative: 10.8 ± 3.7 mm, postoperative: 2.7 ± 3.0 mm; p = 0.003). Among the 11 patients, 5 showed complete resolution of cerebellar tonsillar herniation. CONCLUSIONS Complete PVDO can more efficiently expand the posterior cranial fossa, unlike conventional methods. Moreover, it helps to relieve cerebellar tonsillar herniation. Complete PVDO is a powerful tool to increase the intracranial and posterior fossa volumes in patients with craniosynostosis and concurrent CM-I.


2018 ◽  
Vol 61 (10) ◽  
pp. 2458-2466
Author(s):  
Esther Lázaro ◽  
Maitane García ◽  
Ane Ibarrola ◽  
Imanol Amayra ◽  
Juan Francisco López-Paz ◽  
...  

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