Key result
Immunosuppressive therapy achieves sustained psychiatric and cognitive recovery in misdiagnosed neuropsychiatric lupus.
Why the study?
Neuropsychiatric systemic lupus erythematosus presents diagnostic challenges due to psychiatric symptoms, language barriers, and fragmented care leading to delayed recognition and treatment.
Case Report (n=1)
This case highlights that new-onset or atypical psychosis in the context of recent systemic findings (like pericardial effusion) should prompt evaluation for neuropsychiatric SLE, despite potential diagnostic anchors like prior psychiatric diagnoses.
Supports NPSLE evaluation in atypical psychosis with systemic clues; leaves open need for controlled trials to confirm treatment response.
Neuropsychiatric systemic lupus erythematosus (NPSLE) is a diagnostically complex manifestation of systemic lupus erythematosus (SLE) that may initially present with significant psychiatric symptoms, contributing to delayed recognition and treatment. We describe a 36-year-old non-English-speaking female patient with a recent history of intermittent medical and psychiatric encounters over 1 year, during which progressive psychosis was attributed to a primary psychiatric illness. Her course was characterized by fragmented care across institutions, limited collateral history, language discordance, and diagnostic anchoring on psychiatric diagnosis despite evolving systemic findings. Several weeks after surgical management of a large pericardial effusion, the patient presented to the emergency department with acute psychiatric decompensation marked by hallucinations and behavioral abnormalities. She was admitted for cardiac monitoring and treated for presumed primary psychosis. Subsequent multidisciplinary reassessment, delayed acquisition of outside records, and neuroimaging revealing diffuse parenchymal enhancement raised concern for NPSLE. Once lupus-directed immunosuppressive treatment was initiated, the patient demonstrated substantial improvement in psychiatric symptoms. This vignette highlights the diagnostic challenges of autoimmune disease presenting with psychiatric manifestations and underscores the importance of systematic collateral assessment, cross-institutional communication, and interdisciplinary collaboration in reducing diagnostic delay.
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Negassi et al. (2026) conducted a case report in Neuropsychiatric systemic lupus erythematosus (NPSLE) presenting with psychosis and pericardial effusion (n=1). Lupus-directed immunosuppressive treatment was evaluated on Improvement in psychiatric and cognitive symptoms. Initiation of lupus-directed immunosuppressive treatment led to substantial, sustained improvement in psychiatric and cognitive symptoms in a patient with NPSLE misdiagnosed as primary psychosis.
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