Introduction: CNS infections are an emerging health problem with poor prognosis if the treatment is not prompt and adequate. Thus, establishing a correct diagnosis is necessary to quickly start the appropriate treatment. This study was undertaken to study the etiology and the imaging spectrum of CNSI in and around western Uttar Pradesh in a tertiary health care set up and to correlate the neuro-imaging findings with clinic-pathological data.
Material and Methods:In this Prospective Observational study 80 patients clinically suspected of CNS infection were studied by CT/MRI and the neuro imaging findings were correlated with clinical and CSF findings.Results: Based on clinical features, CSF findings, the treatment given and the response to treatment tuberculous infection (TBM) was most common infection (41.2%) followed by pyogenic meningitis (36.2%) and viral infection (22.5%). In 29 patients of pyogenic CNS infection most common imaging finding was leptomeningitis(62%) followed by pachymeningitis (31%), hydrocephalus (24.1%), abscess (6.8%), post vasculitic infarct(6.8%) and extra axial collection(6.8%). In 33 patients of tubercular CNS infection most common imaging finding was basal leptomeningitis (78.7%) followed by tuberculoma (72.7%), pachymeningitis (33.3%), hydrocephalus (27.2%), abscess (12.1%), post vasculitis infarct (12.1%) and spinal cord involvement in 1 (3%) patient. In the 18 viral CNS infection cases most common imaging finding was parenchymal hyperintensity on MRI or hypodensity on CT with/without peripheral vasogenic edema (94.4%) followed by leptomeningeal/pachymeningeal involvement (61.1%) and post vasculitis infarct (11.1%).
Conclusion:The sensitivity of neuroimaging in pyogenic CNS infection was 81.2% and specificity was 93.7% while sensitivity of neuroimaging in tubercular CNS infection was 88.8% and specificity was 97.8% and in viral CNS infection sensitivity was 84.2% and specificity was 96.7%. There was significant association (p value <0.05) of basal leptomeningitis and granulomas on imaging with tubercular infection and parenchymal signal changes with viral infections.