Characteristic CSF Findings in Guillain-Barré Syndrome
The classic cerebrospinal fluid finding in Guillain-Barré Syndrome is albumino-cytological dissociation, characterized by elevated CSF protein levels with a normal cell count. 1
Key CSF Characteristics in GBS
Primary Diagnostic Finding
- Albumino-cytological dissociation: Elevated CSF protein with normal cell count 1, 2
- First described by Guillain, Barré, and Strohl in their original paper 3
- Serves as a hallmark finding supporting GBS diagnosis
Important Temporal Considerations
- Protein elevation timing:
Cell Count Parameters
- Normal cell count: Typically <5 cells/μl
- Mild pleocytosis (10-50 cells/μl) may be compatible with GBS but should prompt consideration of alternative diagnoses 1
- Marked pleocytosis (>50 cells/μl) suggests alternative pathologies such as:
- Leptomeningeal malignancy
- Infectious or inflammatory diseases of the spinal cord or nerve roots 1
Alternative CSF Measurements
- CSF/serum albumin quotient (Qalb):
Clinical Correlations
- Higher CSF protein levels correlate with:
Important Caveats
- Normal CSF protein does NOT rule out GBS, especially early in the disease course 1
- CSF examination should be performed during initial evaluation primarily to rule out other causes of weakness 1
- B-CSFB (blood-CSF barrier) dysfunction is present in only about half of GBS patients during the first week 4
- Paradoxically, a low B-CSFB dysfunction response during follow-up has been associated with poorer outcomes 4
Practical Application
When evaluating a patient with suspected GBS:
- Perform lumbar puncture as part of initial evaluation
- Look specifically for albumino-cytological dissociation
- If protein is normal but clinical suspicion remains high, consider:
- Timing (may be too early in disease course)
- Repeating CSF analysis after 1-2 weeks if diagnosis remains uncertain
- Be alert to cell counts >50/μl, which should prompt investigation for alternative diagnoses
Remember that while CSF analysis is valuable, it should be interpreted alongside clinical features and electrodiagnostic studies for a comprehensive GBS diagnosis.