Evidence map›Paper›PMID 42416103›Full record

ArticlePCN reports : psychiatry and clinical neurosciences2026

Pre-corticosteroid delusional psychosis and olanzapine-responsive behavioral dyscontrol in autoimmune glial fibrillary acidic protein astrocytopathy: A case report.

Tomomi Sugisaki, Yoshiteru Sato, Hiroaki Fujita, Yasushi Kawamata, Norio Sugawara, Keisuke Suzuki, Norio Yasui-Furukori

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Article in PCN reports : psychiatry and clinical neurosciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Tomomi SugisakiDepartment of Psychiatry Dokkyo Medical University Mibu Tochigi Japan.
Yoshiteru SatoDepartment of Psychiatry Dokkyo Medical University Mibu Tochigi Japan.
Hiroaki FujitaDepartment of Neurology Dokkyo Medical University Mibu Tochigi Japan.
Yasushi KawamataDepartment of Psychiatry Dokkyo Medical University Mibu Tochigi Japan.
Norio SugawaraDepartment of Psychiatry Dokkyo Medical University Mibu Tochigi Japan.ORCID https://orcid.org/0000-0001-7058-664X
Keisuke SuzukiDepartment of Neurology Dokkyo Medical University Mibu Tochigi Japan.
Norio Yasui-FurukoriDepartment of Psychiatry Dokkyo Medical University Mibu Tochigi Japan.ORCID https://orcid.org/0000-0002-4414-3770

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy is an immunotherapy-responsive inflammatory central nervous system disorder. Psychiatric manifestations include delirium, cognitive or behavioral change, apathy, depressive symptoms, and anxiety; however, frank delusional psychosis before corticosteroid exposure is rarely characterized. Timing is critical because corticosteroids can themselves cause psychosis. Case Presentation: A 42-year-old man with no previous psychotic disorder developed a progressive subacute syndrome over several months, beginning with headache and followed by impaired fine motor function, dysarthria, dysphagia, tremor, and cognitive decline. Cerebrospinal fluid (CSF) showed inflammation, and CSF GFAP-immunoglobulin G (IgG) was confirmed by qualitative cell-based and tissue-based assays. Before corticosteroid pulse therapy or oral prednisolone, his family observed a new persecutory delusion that someone was outside the window. Immunotherapy was led by neurologists, and psychiatric symptoms were assessed by psychiatrists through consultation and later psychiatric hospitalization. After corticosteroid therapy, neurological symptoms partially improved, but persecutory ideas, grandiosity, insomnia, irritability, aggression, and escape behavior became prominent. Prednisolone was continued because of the autoimmune neurological disease. Olanzapine was titrated to 15 mg/day. Behavioral dyscontrol improved markedly despite continued prednisolone, and physical restraint was no longer required; however, residual grandiose delusional ideas persisted. Conclusion: This case suggests that delusional psychosis can be an early manifestation of autoimmune GFAP astrocytopathy. Because the first delusion preceded corticosteroid exposure, steroid-induced psychosis was excluded as the mechanism of onset. Olanzapine may stabilize severe behavioral dyscontrol while necessary corticosteroid therapy is maintained, although residual delusions may persist.

Indexed as

autoimmune encephalitisdelusionGFAP astrocytopathyolanzapineorganic psychosis

Identifiers

PMID42416103
PMCPMC13338703

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