What is the characteristic cerebrospinal fluid (CSF) picture in tubercular meningitis?

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Characteristic CSF Picture in Tubercular Meningitis

The characteristic cerebrospinal fluid (CSF) picture in tubercular meningitis includes raised opening pressure, clear or cloudy appearance, lymphocytic pleocytosis (typically 5-500 cells/μL), markedly elevated protein, very low glucose, and very low CSF/plasma glucose ratio. 1

CSF Parameters in Tubercular Meningitis

Opening Pressure and Appearance

  • Opening pressure is typically raised in tubercular meningitis 1
  • CSF appearance is usually clear or cloudy, unlike the turbid or purulent appearance commonly seen in bacterial meningitis 1

Cell Count and Differential

  • CSF white cell count (WCC) is typically elevated, ranging from 5-500 cells/μL 1
  • Lymphocytes predominate in the cell differential, though neutrophils may predominate early in the disease course 1
  • In some cases, CSF WCC may be normal, especially in immunodeficient patients 1
  • Plasmocytes (plasma cells) may appear from the third week of disease in approximately 30% of cases 2

Protein and Glucose

  • CSF protein is markedly raised, typically >1 g/L, which has a sensitivity of 78% and specificity of 94% for diagnosing tubercular meningitis 1, 3
  • CSF glucose is very low, with values typically <2.2 mmol/L (sensitivity 68%, specificity 96%) 1, 3
  • CSF/plasma glucose ratio is very low, typically <0.5 (sensitivity 90%) 1, 3

Diagnostic Considerations

Temporal Evolution of CSF Findings

  • In the first 10 days of disease, neutrophils may predominate (60-80%) 2
  • As the disease progresses, mononuclear cells become predominant, including lymphocytes, lymphoid cells, monocytoid cells, and macrophages 2
  • CSF abnormalities may persist for weeks to months, with pleocytosis sometimes lasting up to two years in atypical cases 2

Diagnostic Challenges

  • CSF acid-fast smear and culture have relatively low sensitivity but yield increases with multiple, large-volume samples 4
  • Nucleic acid amplification tests (PCR) on CSF are highly specific but have suboptimal sensitivity 4
  • In some cases, diagnosis may be delayed until the 37th day or later, as reported in case studies 5

Comparison with Other Types of Meningitis

Parameter Tuberculous Bacterial Viral Fungal
Opening Pressure Raised Raised Normal/mildly raised Raised
Appearance Clear or cloudy Turbid, cloudy Clear Clear or cloudy
WCC (cells/μL) 5-500 >100 5-1000 5-500
Cell type Lymphocytes* Neutrophils Lymphocytes Lymphocytes
Protein (g/L) Markedly raised Raised Mildly raised Raised
Glucose Very low Very low Normal/slightly low Low
CSF/plasma glucose ratio Very low Very low Normal/slightly low Low

*May be neutrophils early in the disease 1

Clinical Pearls and Pitfalls

  • CSF findings alone cannot provide an absolute diagnosis; they must be interpreted in the clinical context 1
  • Early empiric treatment should be initiated as soon as clinical suspicion is supported by initial CSF studies 4
  • Adjunctive corticosteroids have been shown to improve mortality in tubercular meningitis 4, 6
  • A positive TB contact, Mantoux skin test, chest radiograph, CT/MRI brain scan, and demonstration of TB bacilli from extraneural sources are invaluable in supporting a diagnosis of tubercular meningitis 6
  • CSF to serum glucose ratio is more informative than absolute glucose value alone 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

The diagnostic value of cerebrospinal fluid chemistry results in childhood tuberculous meningitis.

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2015

Research

Tuberculous meningitis: diagnosis and treatment overview.

Tuberculosis research and treatment, 2011

Research

Tuberculous meningitis.

Handbook of clinical neurology, 2013

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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