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Chiari 1 deformity in children: etiopathogenesis and radiologic diagnosis
Charles Raybaud1, George I Jallo2
1Neuroradiology, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
Insights
Chiari 1 deformity results from a developmental mismatch, causing cerebellar tonsil herniation. This condition, often asymptomatic, is diagnosed via MRI and assessed by posterior fossa size and craniovertebral joint function.
Area of Science:
- Neurology
- Developmental Biology
- Radiology
Background:
- Normal hindbrain and posterior fossa growth ensures cerebellar tonsils remain above the foramen magnum, allowing free cerebrospinal fluid (CSF) movement.
- Developmental discrepancies, particularly insufficient posterior fossa development, can lead to cerebellar tonsil herniation below the foramen magnum, termed Chiari 1 deformity.
- Chiari 1 deformity is an anatomic diagnosis; many individuals remain asymptomatic, though clinical significance is often associated with tonsil descent exceeding 5 mm.
Purpose of the Study:
- To define the anatomic and clinical characteristics of Chiari 1 deformity.
- To identify radiologic markers indicative of Chiari 1 deformity severity and underlying causes.
- To evaluate the role of posterior fossa morphology and craniovertebral joint function in the pathogenesis of Chiari 1 deformity.
Main Methods:
- Review of magnetic resonance imaging (MRI) findings, including tonsil descent, posterior fossa morphology, and craniovertebral junction abnormalities.
- Assessment of CSF spaces, spinal cord compression, and presence of syringomyelia.
- Radiologic evaluation of posterior fossa dimensions (e.g., posterior fossa pentagon, Chamberlain's line) and craniovertebral joint status (e.g., proatlantal hypoplasia, segmentation abnormalities).
Main Results:
- Chiari 1 deformity is characterized by cerebellar tonsil descent below the foramen magnum, often associated with a shallow posterior fossa and/or craniovertebral joint abnormalities.
- MRI reveals key indicators of severity such as tonsil pegging, CSF space obstruction, cord compression, abnormal cord signal, and syringomyelia, potentially caused by the Venturi effect.
- Radiologic assessment highlights the importance of posterior fossa size and craniovertebral joint function, with conditions like proatlantal hypoplasia leading to osteoneural conflict.
Conclusions:
- Chiari 1 deformity arises from a developmental imbalance between neural and bony structures, primarily affecting the posterior fossa and craniovertebral junction.
- Accurate diagnosis and severity assessment rely on a combination of MRI findings, including tonsil position, posterior fossa morphology, and craniovertebral joint integrity.
- Understanding the etiopathogenesis involving bony structures and CSF dynamics is crucial for managing Chiari 1 deformity and associated conditions like syringomyelia.
Abstract:
The metamerically associated normal hindbrain and normal posterior fossa are programmed to grow together in such a way that the tonsils are located above the foramen magnum and surrounded by the cerebrospinal fluid (CSF) of the cisterna magna. This allows the pulsating CSF to move freely up and down across the craniovertebral junction (CVJ). A developmental mismatch between the rates of growth of the neural tissue and of the bony posterior fossa may result in the cerebellar tonsils being dislocated across the foramen magnum. The cause of this may be, rarely, an overgrowth of the cerebellum. More commonly, it is due to an insufficient development of the posterior fossa, possibly associated with a malformation of the craniocervical joint. When it is not due to a remediable cause, such a herniation is called a Chiari 1 deformity. This definition is anatomic (descent of the tonsils below the plane of the foramen magnum) and not clinical: many patients with the deformity are and will remain asymptomatic. Most authors consider that a descent of 5 mm or more is clinically significant but other factors, such as the diameter of the foramen magnum and the degree of tapering of the upper cervical "funnel," are likely to be as important. Morphologic markers of severity on magnetic resonance imaging are, beside the degree of descent, the peg-like deformity of the tonsils, the obstruction of the surrounding CSF spaces (at the craniocervical junction and in the whole posterior fossa), a compression of the cord, an abnormal signal of the cord, and a syringomyelia, typically cervicothoracic. The syringomyelia is assumed to be explained by the "Venturi effect" that is associated with the increased velocity of the CSF across the restricted CSF spaces. Radiologically, the etiopathogenic assessment should address the size and morphology of the posterior fossa, and the functional status of the craniocervical flexion joint. The posterior fossa is best evaluated on sagittal cuts by the posterior fossa pentagon proportionality associated with the line of Chamberlain, and on coronal cuts, by showing a possible shallowness of the posterior fossa. The functional status of the craniocervical joint is altered in case of a proatlantal hypoplasia, as this condition results in a cranial shift of the joint that brings the tip of the dens and of the flexion axis in front of the medulla, that is, in a situation of osteoneural conflict. Less commonly, similar conflicts may also occur when an abnormal craniocervical segmentation results in an instability of the joint.
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