Kikuchi-Fujimoto Disease with Subsequent Meningoencephalitis Insights into Rare Complications – A Case Report
Abstract
Kikuchi-Fujimoto Disease (KFD) is a rare, benign, self-limiting condition primarily affecting young adults and is often misdiagnosed due to its nonspecific symptoms. We present a rare case of a 36-year-old man who presented with high-grade fever, cervical lymphadenopathy, and weight loss. Despite a comprehensive workup, involving imaging studies and laboratory investigations, the diagnosis remained elusive until a lymph node excisional biopsy confirmed the Kikuchi disease. The patient developed meningoencephalitis, a rare but severe complication of KFD, characterized by seizures and altered mental status.Supportive care including non-steroidal anti-inflammatory drugs, and corticosteroids are the mainstay of management. The patient was discharged with a good prognosis. This case highlights the diagnostic challenges and potential severe neurological complications of KFD, emphasizing the need for heightened awareness and vigilant follow-up.
How to Cite This Article
Khan MA, Kazi A, Sohail M, Aziz A, Zarar F, Saqlain F. Kikuchi-Fujimoto Disease with Subsequent Meningoencephalitis Insights into Rare Complications – A Case Report. J Pak Soc Intern Med. 2024;5(3):649–653. doi:10.70302/jpsim.v5i3.2458
Conflict of Interest
All authors declare no competing interests.
Funding
No specific funding was received for this research.
Funder information follows the Crossref Funder Registry standard.
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