What is the most likely diagnosis for an IV (intravenous) drug user presenting with symptoms of meningitis, including fever and headache for 3 weeks, worsening headache, low cerebrospinal fluid (CSF) glucose, elevated protein, and lymphocytic predominance?

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Tuberculous Meningitis

The most likely diagnosis is B. Tuberculous meningitis, based on the subacute 3-week presentation, lymphocytic predominance, markedly low CSF glucose, elevated protein, and IV drug use risk profile. 1

Key Diagnostic Features Supporting TB Meningitis

The CSF profile is classic for tuberculous meningitis:

  • Lymphocytic predominance is characteristic of TB meningitis, though neutrophils may predominate early in the disease course 1, 2
  • CSF glucose <0.4 mmol/L (assuming this is the CSF value) with a CSF/plasma glucose ratio <0.5 is highly specific for TB meningitis (96% specificity) 1
  • Markedly elevated protein (3 g/L) is typical of TB meningitis, which characteristically shows protein >1 g/L 1
  • Subacute presentation over 3 weeks strongly favors TB meningitis; a clinical history >5 days is independently predictive with 93% sensitivity 1, 3

Why Other Diagnoses Are Excluded

Bacterial meningitis (Option C) is ruled out because:

  • Bacterial meningitis typically shows neutrophil predominance (80-95%), not lymphocytic predominance 4, 1
  • The 3-week subacute course is incompatible with acute bacterial meningitis, which progresses rapidly 4
  • While bacterial meningitis can show low glucose, the CSF/plasma ratio would typically be <0.36, and the lymphocytic predominance makes this diagnosis unlikely 1

Viral meningitis (Option A) is excluded because:

  • Viral meningitis typically presents with normal or only slightly low CSF glucose, with CSF/plasma ratio remaining >0.36 1, 5
  • The markedly elevated protein (3 g/L) far exceeds the mild elevation seen in viral meningitis 5
  • The 3-week progressive course is atypical for viral meningitis 5

Fungal meningitis (Option D) is less likely because:

  • While fungal meningitis can present similarly with lymphocytic predominance and low glucose, TB meningitis is far more common in IV drug users, particularly those with HIV risk 1
  • The specific CSF profile with protein of 3 g/L and the clinical timeline are more characteristic of TB meningitis 2, 6

Critical Clinical Context

IV drug use is a major risk factor for TB meningitis due to:

  • Higher rates of HIV infection in this population, which dramatically increases TB meningitis risk 1
  • HIV testing must be performed immediately in this patient 1

Diagnostic Algorithm Applied

When six features are present, TB meningitis has 93% sensitivity and 77% specificity 3:

  1. ✓ Clinical history >5 days (3 weeks)
  2. ✓ Headache present
  3. ✓ CSF WBC likely <1000/mm³ (lymphocytic predominance suggests moderate elevation)
  4. ✓ Lymphocyte proportion >30%
  5. ✓ Protein >100 mg/dL (3 g/L = 300 mg/dL)
  6. ✓ Low CSF glucose

This patient meets all criteria, confirming TB meningitis as the diagnosis. 3

Critical Management Pitfall

Treatment must be initiated immediately without waiting for culture confirmation, as CSF AFB smear has low sensitivity (positive in only 30% of cases) and culture takes weeks 2, 6. Empiric four-drug therapy (isoniazid, rifampin, pyrazinamide, and ethambutol or streptomycin) plus adjunctive corticosteroids should be started now 2.

References

Guideline

Diagnosis and Management of Tuberculous Meningitis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Tuberculous meningitis: diagnosis and treatment overview.

Tuberculosis research and treatment, 2011

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Viral Meningitis Diagnosis and Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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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