Diagnostic Tests for Cerebellar Lesions
MRI of the brain without contrast is the gold standard imaging modality for evaluating suspected cerebellar lesions, providing superior soft tissue contrast to detect parenchymal injury, volume loss, and signal intensity alterations. 1
Clinical Examination Tests for Cerebellar Function
Coordination Tests
- Finger-to-nose test: Patient alternately touches their nose and the examiner's finger
- Heel-to-shin test: Patient slides heel down opposite shin while lying supine
- Rapid alternating movements: Patient rapidly pronates and supinates hands on thighs
- Dysdiadochokinesia: Inability to perform rapid alternating movements smoothly
Gait and Stance Tests
- Tandem gait (heel-to-toe walking): Reveals wide-based, irregular stepping pattern
- Romberg test: Standing with feet together and eyes closed (cerebellar ataxia persists with eyes open or closed, unlike sensory ataxia)
- Assessment for truncal ataxia: Inability to sit upright without support
Speech and Eye Movement Tests
- Speech assessment: Listen for scanning dysarthria (slow, slurred speech with irregular pauses)
- Nystagmus evaluation: Observe for jerky eye movements, especially gaze-evoked
- Saccadic eye movements: Check for dysmetria of saccades (overshooting or undershooting targets)
Neuroimaging
First-Line Imaging
- MRI brain without contrast: Provides detailed evaluation of cerebellar architecture 1, 2
- T1-weighted images: Assess for structural abnormalities
- T2-weighted/FLAIR images: Detect signal abnormalities, edema
- Diffusion-weighted imaging: Identify acute infarction
- Susceptibility-weighted imaging: Detect hemorrhage or calcification
Additional Imaging Based on Clinical Suspicion
- MRI with contrast: Indicated when neoplasm, infection, or inflammatory conditions are suspected 1
- MRI of cervical and thoracic spine: Consider when spinal cord involvement is suspected (e.g., in spinocerebellar ataxias) 1
- CT head without contrast: May be used in emergency settings or when MRI is contraindicated; helpful for detecting calcifications in certain subtypes of spinocerebellar ataxia 1
- MRA head and neck: Consider when vascular etiology (e.g., posterior circulation stroke) is suspected 1
Laboratory Tests
- Genetic testing: For suspected hereditary ataxias
- Thyroid function tests: To rule out metabolic causes
- Vitamin levels: B12, E, and thiamine deficiencies can cause ataxia
- Ceruloplasmin and copper studies: To rule out Wilson's disease
- Inflammatory markers: ESR, CRP for inflammatory/autoimmune causes
- Paraneoplastic antibody panel: When paraneoplastic cerebellar degeneration is suspected
- CSF analysis: For suspected infection, inflammation, or demyelinating disease
Management Approach Based on Etiology
Acute Cerebellar Lesions
- Stroke: Immediate neuroimaging and stroke protocol management 1
- Hemorrhage: Blood pressure control, reversal of anticoagulation if applicable, surgical evacuation for large cerebellar hemorrhages with brainstem compression 1
- Infection: Antimicrobial therapy based on identified pathogen
- Toxic/metabolic: Removal of offending agent, correction of metabolic abnormalities
Chronic/Progressive Cerebellar Lesions
- Genetic ataxias: Supportive care, genetic counseling
- Tumors: Surgical resection, radiation therapy, chemotherapy based on tumor type
- Autoimmune/inflammatory: Immunomodulatory therapy
- Drug-induced: Discontinuation of offending agent 1
Common Pitfalls and Caveats
- Misdiagnosis: Cerebellar ataxia can be confused with other movement disorders or sensory ataxia
- Incomplete evaluation: Failure to perform comprehensive cerebellar testing may miss subtle signs
- Imaging limitations: CT has limited sensitivity for posterior fossa lesions due to beam-hardening artifacts
- Overlooking associated symptoms: Cerebellar lesions may present with cognitive and affective symptoms beyond motor dysfunction
- Delayed diagnosis: Acute cerebellar lesions, particularly stroke or hemorrhage, require urgent evaluation and management
Specific Cerebellar Syndromes and Their Localization
- Vermis lesions: Primarily cause truncal ataxia, titubation, and gait disturbance 2, 3
- Hemispheric lesions: Primarily cause ipsilateral limb ataxia 3, 4
- Flocculonodular lesions: Associated with vertigo, nystagmus, and lateropulsion 3
- Anterior lobe lesions: Associated with disordered timing of movements 4
- Posterior lobe lesions: Impair motor learning and coordination 4
By systematically evaluating cerebellar function through targeted clinical examination and appropriate imaging, clinicians can accurately diagnose cerebellar lesions and implement appropriate management strategies to improve patient outcomes.