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Table of Contents
Terms Used In This Article
control group - in a research study, a group of people who are
similar to the subjects under study in age and gender but are assumed to be
healthy; the control group serves as a basis for comparison
fossa - a depression
posterior - towards the back
posterior fossa - area of the back of the skull where the cerebellum
is situated
pseudotumor cerebri - condition where the pressure of CSF in the
brain is chronically elevated
skull base - the lower bones of the skull
shunt - a tube like device which is surgically implanted in order to
drain or redirect CSF.
Common Chiari Terms cerebellar tonsils -
portion of the cerebellum located at the bottom, so named because of their
shape
cerebellum - part of
the brain located at the bottom of the skull, near the opening to the spinal
area; important for muscle control, movement, and balance
cerebrospinal fluid (CSF) - clear liquid in the brain and spinal
cord, acts as a shock absorber
Chiari malformation I -
condition where the cerebellar tonsils are displaced out of the skull area
into the spinal area, causing compression of brain tissue and disruption of
CSF flow
decompression surgery -
general term used for any of several surgical techniques employed to
create more space around a Chiari malformation and to relieve compression
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January 31, 2008 -- The underlying causes of Chiari malformation are
not completely understood, and a recent study involving a multi-generational
Chiari family may have confused the picture even more. Some cases of
Chiari are easy to understand, for example a mass in the brain - such as a
tumor or cyst - can push the cerebellum out resulting in Chiari.
However, in many cases the underlying cause is not as clear.
Several theories have been put forth over the years
which may explain Chiari in different subsets of patients (Figure 1).
Some people believe that Chiari may be due to tethering of the spinal cord
which results in downward traction. Other Chiari cases seem to be
linked to altered CSF dynamics, such as with pseudotumor cerebri. The
role of trauma in Chiari, such as with car accidents, is not well understood
but with so many patients reporting trauma as a triggering event, it must be
taken into account by any comprehensive theory. In addition, it
appears there is a genetic component to Chiari. There is now
sufficient evidence to suggest that some percentage of Chiari cases have a
genetic basis. To date, no Chiari gene has been identified, but
scientists have identified specific chromosomes where such genes may be
located.
One leading theory on the underlying cause of Chiari
involves the posterior fossa region of the skull, which is the depression in
the back where the cerebellum is situated. Research has revealed that
on average Chiari patients tend to have small posterior fossas, which has
led some doctors and scientists to describe Chiari as a developmental
problem which results in a skull which is too small for the brain. In
studying this theory, researchers have developed methods to measure the
volume of the posterior fossa from MRI images and have found specific
anatomical features in the base of the skull which tend to be abnormal in
Chiari patients.
Because it arises from embryological development, the
small posterior fossa theory lends itself to having a genetic component.
However, a study of a family with four generations of Chiari patients
published in the January, 2008 issue of the Journal of Neurosurgery:
Pediatrics (Tubbs et al.), shows that with Chiari, nothing is simple.
Specifically, Tubbs used MRI images to measure the posterior fossa volume
of 5 out of 6 affected family members, and compared the results to
age-matched normal controls.
The family included (Figure 2):
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Case 1: A woman who was found to have Chiari upon autopsy and who had no
known symptoms
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Case 2: Her daughter who developed dizziness and neck pain at the age of 56
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Case 3: The son of Case 2, who developed back and neck pain at 40
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Case 4: The daughter of Case 2, who developed headaches at 37
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Cases 5 & 6: The twin sons of Case 4, who developed headaches and neck
pain at 16.
All the family members (except Case 1) were found to have Chiari with
herniations ranging from 6-25mm, and one of the twin boys also had a syrinx.
None of the affected family members had a history of head trauma or other
genetic conditions which could explain the presence of symptomatic Chiari.
Cases 2, 4, 5, and 6 underwent decompression surgery which resolved their
symptoms.
Figure 2: Generational Family Members Affected By Chiari

Note: Black squares/circles are family members with Chiari.
Squares represent males; circles represent females.
The researchers used a well established method to
measure the posterior fossa volume from the MRIs of Cases 2-6. When
they compared the measured volumes to age-matched controls from other
research publications, they found no significant differences. In other
words, all the family members had normal sized posterior fossas.
This is not the first study to question the scope of
the posterior fossa theory. Sgouros found that children with Chiari
only had normal sized posterior fossas, but children with Chiari and
syringomyelia had small posterior fossas. The published research which
has linked small posterior fossas to Chiari tends to average the Chiari
patients together, which can hide the fact that some patients have small
posterior fossas, but others may not.
Although only focused on one family, this study
strongly suggests that even in cases that likely have a genetic component, a
small posterior fossa may not be the problem. As researchers continue
to look for the underlying causes of Chiari, they will need to move beyond
grouping all Chiari cases together and develop ways to separate and classify
them.
-- Rick Labuda
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Key Points
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Several studies have found that on
average people with Chiari have small posterior fossas
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This has led some to describe Chiari
as a developmental problem where the skull is too small for the brain
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Research has also identified a
genetic component to Chiari
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This study looked at the posterior
fossa volumes of a multi-generational family affected by Chiari
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Family members all had normal sized
posterior fossas as compared to age matched controls
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Clearly a different mechanism is
responsible for Chiari in these cases
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There are currently several possible
underlying causes of Chiari which require further investigation
Figure 1
Possible Causes of Chiari Malformation
Note: The above represents a list of
possibilities only. More research is required to further identify and
validate the underlying cause(s) of Chiari.
Source: Tubbs RS, Hill M, Loukas M, Shoja MM, Oakes WJ.
Volumetric analysis of the posterior cranial fossa in a family with four
generations of the Chiari Malformation Type 1. J Neurosurg Ped. 2008 Jan (1
Suppl): 21-24.
Related C&S News
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More Findings Involving Chiari & Abnormal Skull Geometry
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Children With Chiari Symptoms Due To Shunting Found To Have Small
Posterior Fossa Volume
Is Chiari 0 For Real? Research Shows Small Posterior Fossa In Chiari
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Chiari Link To Small Posterior Fossa Confirmed In Adults |