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For further information, see CMDT Part 33-36: Tuberculous Meningitis
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Essentials of Diagnosis
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Gradual onset of listlessness and anorexia
Fever, headache, vomiting, and seizures common
Cranial nerve abnormalities typical
Tuberculous focus may be evident elsewhere
Cerebrospinal fluid shows several hundred lymphocytes per microliter, low glucose, and high protein
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General Considerations
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Onset usually gradual
With listlessness, irritability, anorexia, and fever
Followed by headache, vomiting, convulsions, and coma
In older patients, headache and behavioral changes are prominent early symptoms
Nuchal rigidity and cranial nerve palsies occur as the meningitis progresses
Evidence of active tuberculosis elsewhere or a history of prior tuberculosis is present in up to 75% of patients
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Differential Diagnosis
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May be confused with any other type of meningitis, but the gradual onset, the predominantly lymphocytic pleocytosis of the spinal fluid, and evidence of tuberculosis elsewhere often point to the diagnosis
Chronic lymphocytic meningitis due to
Carcinomatous meningitis
Sarcoidosis
Subdural hematoma
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The spinal fluid is frequently yellowish, with increased pressure, 100–500 cells/mcL (predominantly lymphocytes, though neutrophils may be present early during infection), high protein, and low glucose (Table 30–1)
Acid-fast stains of cerebrospinal fluid usually are negative, and cultures also may be negative in 15–25% of cases
Nucleic acid amplification tests allow for rapid diagnosis, although sensitivity is only 68–80%
The tuberculin skin testing and interferon-gamma release assays do not distinguish between active and latent tuberculosis and are frequently negative in the presence of CNS infection
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