J Pediatr Infect Dis 2018; 13(04): 313-315
DOI: 10.1055/s-0037-1604105
Case Report
Georg Thieme Verlag KG Stuttgart · New York

A Case Report from the City of Biratnagar, Eastern Zone of Nepal: Kikuchi–Fujimoto Disease

Narayan Kumar
1   Department of Medicine, Awadh Narain Memorial Clinic, Biratnagar, Nepal
,
Abhishek Kumar
2   Department of Paediatric Dentistry, Awadh Narain Memorial Clinic, Biratnagar, Nepal
,
Mamta Varma
3   Department of Obstetrics and Gynaecology, Awadh Narain Memorial Clinic, Biratnagar, Nepal
› Author Affiliations
Further Information

Publication History

05 April 2017

27 May 2017

Publication Date:
05 July 2017 (online)

Abstract

Histiocytic necrotizing lymphadenitis, also known as Kikuchi–Fujimoto disease (KFD), is a rare, benign, self-limiting cervical lymphadenitis of unknown etiology that usually presents with lymphadenopathy and fever. This was the case of a 24-year-old, unmarried female who presented with painful neck swelling, fever, and difficulty in swallowing. She had been treated with antibiotics and anti-inflammatory agents with no results. The patient had been suffering for almost 2 months and did not respond to any treatment. Fine-needle aspiration cytology (FNAC) report showed a granulomatous lymphadenitis. Smear for acid-fast bacilli was also negative. The FNAC report was critical for the diagnosis by suggesting the presence of granulomatous tissue against a background of necrosis. The diagnosis of KFD was confirmed after excision biopsy of the lymph node. The patient was treated symptomatically and responded well. Awareness and knowledge of this disease is essential for the diagnosis for physicians and health care workers in this part of the world so that the appropriate treatment can be given.

 
  • References

  • 1 Fujimoto Y, Kozima Y, Yamaguchi K. Cervical subacute necrotizing lymphadenitis: a new clinicopathologic entity. Naika 1972; 20: 920-927
  • 2 Kikuchi M. Lymphadenitis showing focal reticulum cell hyperplasia with nuclear debris and phagocytes: a clinicopathologic study. Acta Hematol Jpn 1972; 35: 379-380
  • 3 Pileri S, Kikuchi M, Helbron D, Lennert K. Histiocytic necrotizing lymphadenitis without granulocytic infiltration. Virchows Arch A Pathol Anat Histol 1982; 395 (03) 257-271
  • 4 Kuo TT. Kikuchi's disease (histiocytic necrotizing lymphadenitis). A clinicopathologic study of 79 cases with an analysis of histologic subtypes, immunohistology, and DNA ploidy. Am J Surg Pathol 1995; 19 (07) 798-809
  • 5 Sudhakar MK, Sathyamurthy P, Indhumati E, Rajendran A, Vivek B. Kikuchi's disease: a case report from South India. Int J Case Rep Images 2011; 2 (01) 15-18
  • 6 Baskota DK. Kikuchi-Fujimoto disease: a rare cause of cervical lymphadenopathy. Nepal Med Coll J 2006; 8 (01) 63-64
  • 7 Maan MA, Hussain T, Hussain A, Shahid M. Kikuchi.s disease - A case report and review of literature. J Pak Assoc Dermatol 2002; 12 (03) 157-159
  • 8 Mamoon N, Haroon A, Luqman M, Jamal S. Kikuchi's disease of lymph nodes. J Coll Physicians Surg Pak 2003; 13 (03) 138-142
  • 9 Dorfman RF, Berry GJ. Kikuchi's histiocytic necrotizing lymphadenitis: an analysis of 108 cases with emphasis on differential diagnosis. Semin Diagn Pathol 1988; 5 (04) 329-345