Case report on Cotard’s syndrome (CS) in a patient with schizophrenia: a rare case from Malaysia

• Published in: The Egyptian Journal of Neurology, Psychiatry and Neurosurgery Vol. 57; no. 1; pp. 1 - 6
• Main Authors: Subhas, Natasha, Naing, Khin Ohnmar, Su, Chaw, Loo, Jiann Lin, Shahbudin, Aishah Farhana, Sivasubramaniam, Vevehkanandar, Thyagarajan, Reenisha
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 03.08.2021; Springer Nature B.V; SpringerOpen
• Subjects: Case Report; Case reports; Cotard’s syndrome; Depression; ECT; Electroconvulsive therapy; Hypochondriac; Medicine; Medicine & Public Health; Neurology; Neurosurgery; Psychiatry; Schizophrenia; Schizophrenia; Cotard’s syndrome; Depression; Hypochondriac; ECT
• ISSN: 1110-1083; 1687-8329
• DOI: 10.1186/s41983-021-00359-4

Background Cotard’s syndrome (CS) is a neuropsychiatric condition marked by nihilistic delusional(s). Due to its rarity, misdiagnosis of the syndrome often occurs. The current case study is of a Malaysian woman who was misdiagnosed for several years by professionals due to the presence of hypochondriac symptoms before receiving the correct diagnosis. Case presentation In this case presentation, we describe the case of L, a 42-year-old Malaysian lady who was first misdiagnosed with depression. The diagnosis of schizophrenia and CS was confirmed after thorough clinical examination, diagnostic investigations, and deliberation at a departmental forum. The patient improved after receiving electroconvulsive therapy (ECT) along with antipsychotic medications. Conclusions This case study highlights the importance of early recognition of CS by professionals as it can save time for both parties when setting up a treatment plan. Essentially, early recognition of CS in schizophrenia is paramount in the process of rapid stabilization through ECT and promotion of patient recovery.