Kikuchi–Fujimoto disease: a case report

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Authors: Mohammed Atiqur Rahman, Kazi Rahila Ferdousi, Sabiha Afrin Tonwi, Bishnu Pada Dey, Rajashish Chakrabortty
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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

Fields of Study & Subjects

Lymphadenopathy Diagnosis and Analysis Histiocytic Disorders and Treatments Viral-associated cancers and disorders

Publication details

Journal / source
BIRDEM Medical Journal
Volume
16
Issue
1
Pages
44–47
Publication date
17 February 2026
Language
EN