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Kikuchi-Fujimoto Disease - A Case Report in a Middle-aged Adult
Adheesh Phalke1, Vijayashree Gokhale1, Nallani Chakravarthi Sai Sirisha1
1Department of General Medicine, Dr. D. Y. Patil Medical College, Hospital and Research Centre, Dr. D. Y. Patil Vidyapeeth, Pune, Maharashtra, India.
Kikuchi-Fujimoto disease (KFD), a rare condition causing lymph node inflammation, can affect adults. Diagnosis requires lymph node biopsy when other tests for infections or cancer are negative.
Area of Science:
- Pathology
- Immunology
- Oncology
Background:
- Kikuchi-Fujimoto disease (KFD) is a rare, benign lymphadenitis often affecting young adults.
- KFD presentation can mimic serious conditions like tuberculosis and lymphoma, complicating diagnosis.
- This case highlights KFD in a middle-aged adult, expanding its typical demographic.
Purpose of the Study:
- To report a case of KFD in a middle-aged adult.
- To emphasize KFD in the differential diagnosis of cervical lymphadenopathy.
- To underscore the diagnostic value of lymph node biopsy.
Main Methods:
- Clinical presentation of a 46-year-old female with cervical lymphadenopathy and fever.
- Diagnostic workup including tuberculosis screening (GeneXpert, Mantoux, culture) and imaging (ultrasonography, CT).
- Excisional lymph node biopsy for histopathological examination.
Main Results:
- Tuberculosis and malignancy workup were negative.
- Imaging showed multiple necrotic cervical lymph nodes.
- Histopathology revealed features consistent with KFD: necrosis, histiocyte/immunoblast proliferation, and lack of neutrophils.
Conclusions:
- Kikuchi-Fujimoto disease should be considered in adults with cervical lymphadenopathy, especially with negative routine investigations.
- Excisional lymph node biopsy is crucial for definitive KFD diagnosis.
- Symptomatic treatment led to complete resolution in this case.
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