Case Report
Volume: 9 | Issue: 6 | Published: Jul 25, 2025 | Pages: 130 - 134 | DOI: 10.24911/ejmcr.9-2073
Immunosuppressant therapyinduced posterior reversible encephalopathy syndrome: an emerging cause, a rare case report
Authors:
Vinay Kumar Rastog
, Paras Passi
, Shashank Sadhwani
, Prashant Surolia
Article Info
Authors
Vinay Kumar Rastog
Consultant, General Medicine, Jaipur Golden Hospital, Delhi, India
Paras Passi
Consultant, General Medicine, Jaipur Golden Hospital, Delhi, India
Prashant Surolia
General Medicine Trainee, Jaipur Golden Hospital, Delhi, India
Publication History
Received: April 10, 2025
Accepted: June 12, 2025
Published: July 25, 2025
Abstract
Background: Posterior reversible encephalopathy syndrome (PRES) is an acute or subacute cerebral syndrome, the main manifestations of which are headache, encephalopathy, seizures, or visual disturbances in various combinations; this case describes PRES related to drugs and toxic agents.
Case Presentation: We present a case of a 61-year-old female with a history of rheumatoid arthritis, hypothyroidism, dyslipidemia, and drug-induced neutropenia who developed PRES following the use of tab leflunomide. The patient presented with intense generalized itching, erythematous rash, and acute headache, progressing to confusion. Neuroimaging revealed leptomeningeal enhancement in the parieto-occipital regions, consistent with PRES. Prompt treatment with pulse steroid therapy, antihypertensive, and discontinuation of the tab leflunomide led to complete recovery.
Conclusion: This case highlights the importance of early recognition and management of triggering agent causing PRES in patients with autoimmune diseases on immunosuppressant therapy.
Keywords: Hypothyroidism, immunosuppressant therapy, posterior reversible encephalopathy syndrome (PRES), rheumatoid arthritis, case report.
Pubmed Style
Vinay Kumar Rastog, Paras Passi, Shashank Sadhwani, Prashant Surolia. Immunosuppressant therapyinduced posterior reversible encephalopathy syndrome: an emerging cause, a rare case report. EJMCR. 2025; 25 (July 2025): 130-134. doi:10.24911/ejmcr.9-2073
Web Style
Vinay Kumar Rastog, Paras Passi, Shashank Sadhwani, Prashant Surolia. Immunosuppressant therapyinduced posterior reversible encephalopathy syndrome: an emerging cause, a rare case report. https://www.ejmcr.com/articles/2073 [Access: August 14, 2025]. doi:10.24911/ejmcr.9-2073
AMA (American Medical Association) Style
Vinay Kumar Rastog, Paras Passi, Shashank Sadhwani, Prashant Surolia. Immunosuppressant therapyinduced posterior reversible encephalopathy syndrome: an emerging cause, a rare case report. EJMCR. 2025; 25 (July 2025): 130-134. doi:10.24911/ejmcr.9-2073
Vancouver/ICMJE Style
Vinay Kumar Rastog, Paras Passi, Shashank Sadhwani, Prashant Surolia. Immunosuppressant therapyinduced posterior reversible encephalopathy syndrome: an emerging cause, a rare case report. EJMCR. (2025), [cited August 14, 2025]; 25 (July 2025): 130-134. doi:10.24911/ejmcr.9-2073
Harvard Style
Vinay Kumar Rastog, Paras Passi, Shashank Sadhwani, Prashant Surolia (2025) Immunosuppressant therapyinduced posterior reversible encephalopathy syndrome: an emerging cause, a rare case report. EJMCR, 25 (July 2025): 130-134. doi:10.24911/ejmcr.9-2073
Chicago Style
Vinay Kumar Rastog, Paras Passi, Shashank Sadhwani, Prashant Surolia. "Immunosuppressant therapyinduced posterior reversible encephalopathy syndrome: an emerging cause, a rare case report." 25 (2025), 130-134. doi:10.24911/ejmcr.9-2073
MLA (The Modern Language Association) Style
Vinay Kumar Rastog, Paras Passi, Shashank Sadhwani, Prashant Surolia. "Immunosuppressant therapyinduced posterior reversible encephalopathy syndrome: an emerging cause, a rare case report." 25.July 2025 (2025), 130-134. Print. doi:10.24911/ejmcr.9-2073
APA (American Psychological Association) Style
Vinay Kumar Rastog, Paras Passi, Shashank Sadhwani, Prashant Surolia (2025) Immunosuppressant therapyinduced posterior reversible encephalopathy syndrome: an emerging cause, a rare case report. , 25 (July 2025), 130-134. doi:10.24911/ejmcr.9-2073