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Neurodevelopmental and Psychiatric Symptoms in Patients with a Cyst Compressing the Cerebellum: an Ongoing Enigma
Xavier Guell1,2,3, Sheeba A Anteraper4,5,6, Satrajit S Ghosh4,7
1McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA. xaviergp@mit.edu.
Insights
Posterior fossa arachnoid cysts (PFAC) may be linked to cerebellar dysfunction and neurodevelopmental issues. This study used fMRI and genetic testing to explore this complex relationship in a patient with cognitive and psychiatric symptoms.
Area of Science:
- Neuroscience
- Developmental Neuroscience
- Neuroimaging
Background:
- Posterior fossa arachnoid cysts (PFAC) are sometimes found incidentally in patients with neurodevelopmental and psychiatric symptoms.
- The potential causal link between PFAC, cerebellar dysfunction, and neuropsychiatric conditions remains unclear.
Abstract:
A patient diagnosed with developmental delay, intellectual disability, and autistic and obsessive-compulsive symptoms was found to have a posterior fossa arachnoid cyst (PFAC) compressing the cerebellum. The patient was referred to our Ataxia Unit for consideration of surgical drainage of the cyst to improve his clinical constellation. This scenario led to an in-depth analysis including a literature review, functional resting-state MRI analysis of our patient compared to a group of controls, and genetic testing. While it is reasonable to consider that there may be a causal relationship between PFAC and neurodevelopmental or psychiatric symptoms in some patients, there is also a nontrivial prevalence of PFAC in the asymptomatic population and a significant possibility that many PFAC are incidental findings in the context of primary cognitive or psychiatric symptoms. Our functional MRI analysis is the first to examine brain function, and to report cerebellar dysfunction, in a patient presenting with cognitive/psychiatric symptoms found to have a structural abnormality compressing the cerebellum. These neuroimaging findings are inherently limited due to their correlational nature but provide unprecedented evidence suggesting that cerebellar compression may be associated with cerebellar dysfunction. Exome gene sequencing revealed additional etiological possibilities, highlighting the complexity of this field of cerebellar clinical and scientific practice. Our findings and discussion may guide future investigations addressing an important knowledge gap-namely, is there a link between cerebellar compression (including arachnoid cysts and possibly other forms of cerebellar compression such as Chiari malformation), cerebellar dysfunction (including fMRI abnormalities reported here), and neuropsychiatric symptoms?
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