Case Report

A Rare Cause of Prolonged Fever and Cervical Lymphadenopathy: Kikuchi Fujimoto Disease

Volume: 24 Number: 4 February 24, 2025
EN

A Rare Cause of Prolonged Fever and Cervical Lymphadenopathy: Kikuchi Fujimoto Disease

Abstract

Kikuchi Fujimato Disease (KFD) is a rare and benign cause of cervical lymphadenopathy associated with fever. It is important to be aware of this disease as it is included in the differential diagnosis of diseases with high morbidity and mortality, such as lymphoma and tuberculosis. This study presents a child diagnosed with KFD to raise awareness of the disease. A 15-year-old female patient was admitted with neck swelling, weight loss, and fever for three weeks without response to antibiotic treatment. On examination, her temperature was 38oC, she had 3-4 fixed, painful, and hard cervical lymph nodes in cervical chains, the spleen was palpable at 1.5 cm, the liver at 1 cm, and other systems examination was normal. Laboratory tests revealed a neutrophil count of 770/L, lymphocyte of 800/L, C-reactive protein of 16.99 mg/L, and erythrocyte sedimentation rate (ESR) of 120 mm/h. Her fever and fatigue persisted during hospitalization, and no tests reveals infectious diseases. Peripheral blood smears, bone marrow aspiration microscopy, and flow cytometry did not reveal any findings in favor of malignancy, and excisional lymph node biopsy was performed for diagnosis. Histopathological examination was consistent with Kikuchi Fujimoto Disease. Antinuclear antibody (ANA) positivity (+++). The patient’s fever and partial lymphadenopathy resolved after 14 days of hospitalization, and the ESR decreased to 40 mm/h at 4 months. Systemic lupus erythematous (SLE) and hemophagocytosis can complicated KFD, so the follow-up patient continues. It is difficult to distinguish KFD from serious diseases clinically and in the laboratory. Differential diagnosis through histopathological evaluation is associated with the awareness of the clinician and the experience of the pathologist. With an early diagnosis, unnecessary examinations and treatments can be prevented.

Keywords

References

  1. Kikuchi M. Lymphadenitis showing focal reticulum cell hyperplasia with nuclear debris and phagocytes: a clinicopathological study. Acta Hematol Jpn. 1972;35:379-380. google scholar
  2. Fujimoto Y, Kozima Y, Yamaguchi K. Cervical subacute necrotizing lymphadenitis: a new clinicopathologic entity. Naika. 1972;20:920-927. google scholar
  3. Iguchi H, Sunami K, Yamane H, Konishi K, Takayama M, Nakai Y, et al. Apoptotic cell death in Kikuchi’s disease: a TEM study. Acta Otolaryngol Suppl. 1998;538:250. google scholar
  4. Ura H, Yamada N, Torii H, Imakado S, Iozumi K, Shimada S. Histiocytic necrotizing lymphadenitis (Kikuchi’s disease): the necrotic appearance of the lymph node cells is caused by apoptosis. . J Dermatol. 1999;26(6):385. google scholar
  5. Lin HC, Su CY, Huang CC, Hwang CF, Chien CY . Kikuchi’s disease: a review and analysis of 61 cases. Otolaryngol Head Neck Surg. 2003;128(5):650. google scholar
  6. Dumas G, Prendki V, Haroche J, Amoura Z, Cacoub P, Galicier L, et al. Kikuchi-Fujimoto disease: retrospective study of 91 cases and review of the literature. Medicine (Baltimore). 2014;93(24):372. google scholar
  7. Ahn SS, Lee B, Kim D, Jung SM, Lee S-W, Park M-C, et al. Evaluation of macrophage activation syndrome in hospitalised patients with Kikuchi-Fujimoto disease based on the 2016 EULAR/ACR/PRINTO classification criteria. PLoS One 2019; 14(e0219970). google scholar
  8. Lin HC, Su CY, Huang CC, Hwang C-F, Chein C-Y. Kikuchi’s disease: a review and analysis of 61 cases. Otolaryngol Head Neck Surg 2003; 128(650). google scholar

Details

Primary Language

English

Subjects

Pediatric Infectious Diseases

Journal Section

Case Report

Publication Date

February 24, 2025

Submission Date

October 23, 2024

Acceptance Date

December 2, 2024

Published in Issue

Year 2024 Volume: 24 Number: 4

APA
Tural, M. S., Öcal Demir, S., Canbolat, A., & Çobanoğlu Şimşek, B. (2025). A Rare Cause of Prolonged Fever and Cervical Lymphadenopathy: Kikuchi Fujimoto Disease. Çocuk Dergisi, 24(4), 248-251. https://doi.org/10.26650/jchild.2024.1572282
AMA
1.Tural MS, Öcal Demir S, Canbolat A, Çobanoğlu Şimşek B. A Rare Cause of Prolonged Fever and Cervical Lymphadenopathy: Kikuchi Fujimoto Disease. Çocuk Dergisi. 2025;24(4):248-251. doi:10.26650/jchild.2024.1572282
Chicago
Tural, Mustafa Safa, Sevliya Öcal Demir, Aylin Canbolat, and Bengü Çobanoğlu Şimşek. 2025. “A Rare Cause of Prolonged Fever and Cervical Lymphadenopathy: Kikuchi Fujimoto Disease”. Çocuk Dergisi 24 (4): 248-51. https://doi.org/10.26650/jchild.2024.1572282.
EndNote
Tural MS, Öcal Demir S, Canbolat A, Çobanoğlu Şimşek B (February 1, 2025) A Rare Cause of Prolonged Fever and Cervical Lymphadenopathy: Kikuchi Fujimoto Disease. Çocuk Dergisi 24 4 248–251.
IEEE
[1]M. S. Tural, S. Öcal Demir, A. Canbolat, and B. Çobanoğlu Şimşek, “A Rare Cause of Prolonged Fever and Cervical Lymphadenopathy: Kikuchi Fujimoto Disease”, Çocuk Dergisi, vol. 24, no. 4, pp. 248–251, Feb. 2025, doi: 10.26650/jchild.2024.1572282.
ISNAD
Tural, Mustafa Safa - Öcal Demir, Sevliya - Canbolat, Aylin - Çobanoğlu Şimşek, Bengü. “A Rare Cause of Prolonged Fever and Cervical Lymphadenopathy: Kikuchi Fujimoto Disease”. Çocuk Dergisi 24/4 (February 1, 2025): 248-251. https://doi.org/10.26650/jchild.2024.1572282.
JAMA
1.Tural MS, Öcal Demir S, Canbolat A, Çobanoğlu Şimşek B. A Rare Cause of Prolonged Fever and Cervical Lymphadenopathy: Kikuchi Fujimoto Disease. Çocuk Dergisi. 2025;24:248–251.
MLA
Tural, Mustafa Safa, et al. “A Rare Cause of Prolonged Fever and Cervical Lymphadenopathy: Kikuchi Fujimoto Disease”. Çocuk Dergisi, vol. 24, no. 4, Feb. 2025, pp. 248-51, doi:10.26650/jchild.2024.1572282.
Vancouver
1.Mustafa Safa Tural, Sevliya Öcal Demir, Aylin Canbolat, Bengü Çobanoğlu Şimşek. A Rare Cause of Prolonged Fever and Cervical Lymphadenopathy: Kikuchi Fujimoto Disease. Çocuk Dergisi. 2025 Feb. 1;24(4):248-51. doi:10.26650/jchild.2024.1572282