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Psychiatry · Organic psychiatry: autoimmune encephalitis
Sample itemA 23-year-old woman develops, over two weeks, agitation, paranoid delusions and insomnia after a flu-like illness, followed by seizures, orofacial dyskinesias and autonomic instability. MRI is normal and CSF shows lymphocytic pleocytosis. What is the most likely diagnosis and the key additional step?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
A. Anti-NMDA receptor encephalitis, with a search for an ovarian teratoma and immunotherapy
Anti-NMDA receptor encephalitis typically affects young women, with a psychiatric prodrome followed by seizures, dyskinesias, decreased consciousness and autonomic instability. Antibodies against the GluN1 subunit are found in CSF. An ovarian teratoma is present in a substantial proportion of young women, and its removal with immunotherapy (steroids, IVIG or plasma exchange, then rituximab or cyclophosphamide) improves outcomes. Antipsychotics are poorly tolerated and may worsen movement abnormalities.
Option by option
A. Anti-NMDA receptor encephalitis, with a search for an ovarian teratoma and immunotherapy (correct)
Correct. This combination of features and demographics suggests this antibody-mediated encephalitis, needing tumour screening and immunotherapy.
B. Herpes simplex encephalitis, with no further tests
HSV encephalitis typically shows temporal lobe abnormalities on MRI and should be covered with acyclovir while this is excluded.
C. First-episode schizophrenia, with long-term antipsychotic therapy alone
Schizophrenia does not cause seizures, dyskinesias and CSF pleocytosis.
D. Neuroleptic malignant syndrome, with dantrolene
NMS follows antipsychotic exposure with rigidity, fever and raised creatine kinase.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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