Kikuchi Fujimoto Disease: The First Reported Case in Mongolia
DOI:
https://doi.org/10.24079/cajms.2017.06.012Keywords:
Histiocytic Necrotizing Lymphadenitis, Kikuchi Disease, Kikuchi Necrotizing Lymphadenitis, Kikuchi-Fujimoto’s DiseaseAbstract
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.
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Copyright (c) 2017 Mongolian National University of Medical Sciences
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.