Objectives: Kikuchi-Fujimoto Disease (KFD) is a rare, benign condition of necrotising histiocytic lymphadenitis, typically presenting in young women. This report is on the first diagnosed case of KFD in Mongolia. Methods: The patient was a 24-year-old female, who presented with fever, night sweats, rash, and cervical lymphadenopathy. Based on clinical features, histopathology, and immunohistochemistry findings, the diagnosis of KFD was confirmed. Results: Full recovery was achieved using symptomatic treatment. Conclusion: To minimize diagnostic confusion and potentially harmful and unnecessary treatments, we emphasize that clinicians should be aware of this condition.
CITATION STYLE
Altangerel, O., Khatanbaatar, G., Natsagdorj, M.-E., & Gantulga, T. (2017). Kikuchi Fujimoto Disease: The First Reported Case in Mongolia. Central Asian Journal of Medical Sciences, 3(2), 185–189. https://doi.org/10.24079/cajms.2017.06.012
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