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ArticleFrontiers in psychiatry2026

Case Report: Cotard's syndrome associated with suicide attempt-related delirium.

Richárd Flach, Júlia Éva Varga, Róbert Herold, Vita Bányavölgyi, Péter Osvath, Sándor Fekete, Viktor Voros, Tamás Tényi

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Article in Frontiers in psychiatry, 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

8 authors.

Richárd FlachDepartment of Psychiatry and Psychotherapy, Medical School, University of Pécs, Pécs, Hungary.
Júlia Éva VargaDepartment of Psychiatry and Psychotherapy, Medical School, University of Pécs, Pécs, Hungary.
Róbert HeroldDepartment of Psychiatry and Psychotherapy, Medical School, University of Pécs, Pécs, Hungary.
Vita BányavölgyiDepartment of Psychiatry and Psychotherapy, Medical School, University of Pécs, Pécs, Hungary.
Péter OsvathDepartment of Psychiatry and Psychotherapy, Medical School, University of Pécs, Pécs, Hungary.
Sándor FeketeDepartment of Psychiatry and Psychotherapy, Medical School, University of Pécs, Pécs, Hungary.
Viktor VorosDepartment of Psychiatry and Psychotherapy, Medical School, University of Pécs, Pécs, Hungary.
Tamás TényiDepartment of Psychiatry and Psychotherapy, Medical School, University of Pécs, Pécs, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cotard's syndrome is a rare psychopathological phenomenon characterized by nihilistic delusions concerning one's body, existence, or death. We report the case of an 88-year-old man with no previous psychiatric treatment who was admitted following a medication-overdose suicide attempt in the context of a severe depressive crisis. After intensive and internal medical treatment, he developed a fluctuating confusional state characterized by disturbances of orientation, impaired attention, paranoid ideation, and nihilistic beliefs. During this period, he repeatedly stated that he was dead, had been cremated, and that his wife had also died. Notably, these nihilistic beliefs persisted during relatively lucid intervals, even as the severity of the disturbance of consciousness fluctuated. Severe depressive symptoms, somatic decompensation, metabolic abnormalities, sensory impairment, frontotemporal atrophy, and mild neurocognitive impairment were present. The clinical picture was interpreted as Cotard-type nihilistic delusions emerging during a fluctuating delirious state in the context of severe depression, suicidal behavior, and underlying neurocognitive vulnerability. Treatment with risperidone, mirtazapine, somatic stabilization, and supportive psychotherapy was followed by gradual resolution of both the confusional state and the nihilistic delusions. This case highlights the complex interplay between delirium, severe depression, suicidal behavior, and neurocognitive impairment in the development of Cotard-type phenomena and underscores the importance of a careful differential diagnostic approach when nihilistic delusions arise in medically and cognitively vulnerable older adults.

Indexed as

Cotard’s syndromelate-life psychosismild cognitive impairmentnihilistic delusionssuicide attempt

Identifiers

PMID42491005
PMCPMC13375714

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