The posterior inferior cerebellar arteries. Some quantitative observations in posterior cranial fossa tumours and the Arnold-Chiari malformation

1970 ◽  
Vol 21 (1) ◽  
pp. 1-9 ◽  
Author(s):  
J.V. Occleshaw
2021 ◽  
Author(s):  
Estelle Anne How Hong ◽  
Shalid Ahmed ◽  
Srihari Deepak ◽  
Gueorgui Kounin

Abstract Background Syringomyelia is a fluid-filled cyst within the spinal cord and usually associated with Arnold-Chiari malformation. Posterior cranial fossa tumours are a rare cause of tonsillar herniation and secondary syringomyelia. Case Presentation: We report a rare case of a 56-year-old female with posterior cranial meningioma and secondary syringomyelia, admitted with headache, nausea, vomiting, and ataxic gait. MRI demonstrated a large posterior fossa lesion causing early ventriculomegaly and syrinx within the upper spinal cord extending from the hindbrain inferiorly to the level of T8. She underwent a posterior fossa craniectomy with left C1 hemilaminectomy and complete excision of the tumour. In 6 months following her procedure, MRI scan showed a significant reduction in the calibre of the syringomyelia throughout its length and there was a significant improvement in symptoms. Literature review: A PubMed literature search was carried out with keywords: “syringomyelia”, “posterior fossa” and “tumour”. 120 articles were reviewed. The inclusion criteria for this study was posterior fossa meningioma causing syrinx formation. A total of 9 isolated similar cases were identified. Discussion Tonsillar herniation and syringomyelia secondary to posterior cranial fossa meningioma are rare. The alteration in the dynamic flow of CSF is likely to be the cause for the formation and enlargement of the syrinx. Conclusion Although the pathophysiology of syrinx formation is still poorly understood, the alteration of CSF dynamic has been implicated, but a common unifying cause appears to be increased transcranial difference in intracranial pressure across the foramen magnum causing tonsillar herniation, irrespective of location in the posterior fossa. Posterior fossa craniotomy and excision of the lesion is the mainstay treatment.


1993 ◽  
Vol 35 (4) ◽  
pp. 274-278 ◽  
Author(s):  
T. Chang ◽  
M. M. H. Teng ◽  
J. F. Lirng

1999 ◽  
Vol 12 (2_suppl) ◽  
pp. 97-99
Author(s):  
M. Nishikawa ◽  
H. Sakamoto ◽  
A. Hakuba ◽  
N. Nakanishi ◽  
Y. Inoue

2004 ◽  
Vol 46 (3) ◽  
pp. 219-223 ◽  
Author(s):  
M. Warmuth-Metz ◽  
J. K�hl ◽  
J. Krauss ◽  
L. Solymosi

Author(s):  
Nicholas Shaffer ◽  
George Poppe ◽  
Francis Loth ◽  
Oliver Wieben ◽  
Victor Haughton ◽  
...  

Type I Chiari malformation (CM) is a complex disorder of the craniospinal system characterized by underdevelopment of the posterior cranial fossa and overcrowding of the normally developed hindbrain [1], and may be a precursor to more severe secondary disorders such as syringomyelia and hydrocephalus. Diagnosis of CM has proven to be difficult and may often take years to properly identify, as associated neurological symptoms may vary widely and overlap with symptoms of other disorders. Current methods of quantifying the severity of CM, such as radiographical measurement of the depth of hindbrain herniation into the spinal canal or measurement of posterior cranial fossa volume do not necessarily correlate to the symptom severity. Hence, there exists a need for a quantitative diagnostic method which may better characterize the severity of CM and, potentially, help neurosurgeons determine candidates for surgical treatment.


2009 ◽  
Vol 111 (5) ◽  
pp. 1046-1052 ◽  
Author(s):  
Rémy Noudel ◽  
Nicolas Jovenin ◽  
Cristophe Eap ◽  
Bernard Scherpereel ◽  
Laurent Pierot ◽  
...  

Object The chronic tonsillar herniation defining Chiari malformation Type I (CMI) is thought to result from overcrowding of a normally developing hindbrain within a congenitally small posterior cranial fossa (PCF) due to occipital hypoplasia. The goals in the present study were to authenticate the cranioencephalic disproportion in a group of patients with CMI and to discuss new developmental aspects according to which part of the occipital bone was underdeveloped. Methods The authors retrospectively examined a group of 17 patients with CMI. Measurements of osteotentorial and neural structures of the PCF were made on MR images of the brain. The results were compared with findings in 30 healthy controls by using the Mann-Whitney U-test. Results Dimensions of the neural structures did not differ between the 2 groups of patients. The mean length of the basiocciput was significantly shorter in the CMI group (19.4 mm) compared with the control group (25.7 mm; p = 0.0003). The mean diameter of the foramen magnum was larger in the CMI group, but this difference was not statistically significant. The dimensions of the supraocciput and the mean angle of the cerebellar tentorium were identical in the 2 groups. Conclusions Data in this study support the idea that occipital hypoplasia is the main cause of overcrowding within the PCF. Basioccipital shortness is a cardinal feature of the resultant shallow PCF and could proceed from a congenital disorder of the cephalic mesoderm of the parachordal plate or occur later in the infancy because of premature stenosis of the sphenooccipital synchondrosis.


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