A Case Report of Kikuchi-Fujimoto Disease with Immune Thrombocytopenic Purpura. |
Won Yong Kim, Seung Beom Lee, Jun Jeong Choi, Hee Cheol Kang |
1Department of Family Medicine, Yonsei University College of Medicine, Seoul, Korea. kanghc@yuhs.ac 2Department of Pathology, Severance Hospital, Seoul, Korea. |
면역 혈소판감소 자색반을 동반한 Kikuchi병 1예 |
김원용, 이승범, 최준정, 강희철 |
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Abstract |
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. |
Key Words:
Kikuchi-Fujimoto Disease; Histiocytic Necrotizing Lymphadenitis; Immune Thrombocytopenic Purpura |
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