Of 166 patients with a final diagnosis of encephalitis, 56 (33.7%) was infectious, 32 (19.3%) autoimmune, and 48 (28.9%) had encephalitis of unknown cause. Seven patients fulfilled diagnostic criteria for ‘definite’, 10 ‘probable’ and 27 ‘possible’ autoimmune encephalitis. Four had probable viral encephalitis. Thirty (62.5%) were female. There were no significant demographic differences amongst the groups. Confusion and other cognitive abnormalities were the most common symptoms. Seizures were present in 58.3%. Eighteen (37.5%), including 5 of 8 with ‘definite’ seronegative autoimmune encephalitis required intensive care unit support. Twenty-five (52.1%) received immunomodulatory treatment. Methylprednisolone was the most common acute immunosuppressant, azathioprine the most common long-term. Mortality was 10.4% (5 patients). Eight (16.7%) had a clinical relapse. Seventeen were initially diagnosed as having encephalitis of unknown cause, but had an alternative final diagnosis. Four were due to CNS vasculitis, 2 due to primary CNS neoplasms, 2 neuro-syphilis and 9 other causes.