• KAFM
  • Contact us
  • E-Submission
ABOUT
ARTICLE CATEGORY
BROWSE ARTICLES
AUTHOR INFORMATION

Articles

Case Report

A Case Report of Kikuchi-Fujimoto Disease with Immune Thrombocytopenic Purpura.

Won Yong Kim, Seung Beom Lee, Jun Jeong Choi, Hee Cheol Kang
Korean Journal of Family Medicine 2010;31(1):51-55.
Published online: January 20, 2010
1Department of Family Medicine, Yonsei University College of Medicine, Seoul, Korea. kanghc@yuhs.ac
2Department of Pathology, Severance Hospital, Seoul, Korea.
연세대학교 의과대학 가정의학교실, 1연세대학교 세브란스병원 진단병리과
  • 3,992 Views
  • 17 Download
  • 1 Crossref
  • 1 Scopus
prev next

Kikuchi-Fujimoto disease (histiocytic necrotizing lymphadenitis) is a rare disease characterized by lymphadenitis with fever. It is self-limited within one to four months, and is generally diagnosed by an excisional biopsy of the affected lymph node. Kikuchi-Fujimoto disease has a wide variety of nonspecifi c symptoms and it is sometimes misdiagnosed as malignant lymphoma, lymph node tuberculosis, or systemic lupus erythematosus. Because clinical course and treatment of this disease differ from those of others, Kikuchi-Fujimoto disease must be included in differential diagnosis of enlarged lymph node. In this report, we discribed a case of 24-year-old male patient who visited the clinic complaining of fever, petechiae, and enlarged lymph node. He was diagnosed as Kikuchi-Fujimoto disease and immune thrombocytopenic purpura.

TOP