Kikuchi–Fujimoto disease: a case report

Authors

  • Mohammed Atiqur Rahman Professor, Department of Respiratory Medicine, Bangladesh Medical University, Dhaka, Bangladesh.
  • Kazi Rahila Ferdousi PhD student, Department of Cardiology, Bangladesh Medical University, Dhaka, Bangladesh.
  • Sabiha Afrin Tonwi
  • Bishnu Pada Dey Associate Professor, Department of Pathology, Bangladesh Medical University, Dhaka, Bangladesh.
  • Rajashish Chakrabortty Associate Professor, Department of Respiratory Medicine, Bangladesh Medical University, Dhaka, Bangladesh.

DOI:

https://doi.org/10.3329/birdem.v16i1.87671

Keywords:

Kikuchi–Fujimoto disease, necrotizing lymphadenitis, cervical lymphadenopathy

Abstract

Kikuchi–Fujimoto disease (KFD) or histiocytic necrotizing lymphadenitis is a rare, benign, self-limiting disorder that typically presents with cervical lymphadenopathy and fever. Because of its clinical similarity to infectious, autoimmune or malignant conditions, misdiagnosis is common. We report a case of a 41-year-old male presenting with unilateral cervical lymphadenopathy, fever and night sweats. Excisional lymph node biopsy and histopathology revealed features consistent with KFD, including necrotizing lymphadenitis with karyorrhectic debris and crescentic histiocytes without neutrophilic infiltration. Awareness regarding KFD is essential for clinicians and pathologists to avoid unnecessary interventions such as prolonged antibiotic therapy or chemotherapy. Early histopathologically confirmation can significantly reduce patient morbidity and healthcare costs.

BIRDEM Med J 2026; 16(1): 44-47

 

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Published

2026-02-17

How to Cite

Rahman, M. A., Ferdousi, K. R., Tonwi, S. A., Dey, B. P., & Chakrabortty, R. (2026). Kikuchi–Fujimoto disease: a case report. BIRDEM Medical Journal, 16(1), 44–47. https://doi.org/10.3329/birdem.v16i1.87671

Issue

Section

Case Reports