Kikuchi-Fujimoto disease with prolonged fever in children

被引:55
作者
Lee, KY [1 ]
Yeon, YH [1 ]
Lee, BC [1 ]
机构
[1] Catholic Univ Korea, Coll Med, Dept Pediat, Seoul, South Korea
关键词
Kikuchi-Fujimoto disease; subacute necrotizing lymphadenitis; prednisolone;
D O I
10.1542/peds.2004-0485
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
We reviewed 12 patients who had Kikuchi-Fujimoto disease (KFD) and presented with prolonged fever and lymphadenopathy. The clinical and laboratory aspects of the patients confirmed by excisional lymph node biopsy were analyzed. The mean age of the children was 11.0+/-3.0 years (range: 6-15 years). The male-to-female ratio was 1.4:1. The median duration of fever before admission and the total duration of fever was 13 days (range: 7-65 days) and 19.5 days (range: 9-75 days), respectively. One patient had supraclavicular lymphadenopathy, 10 had cervical involvement, and 1 had axillary lymphadenopathy. All of the histologic findings of the lymph node biopsies showed the characteristic findings consistent with KFD, such as paracortical necrosis with karyorrhexis and an increase in the number of phagocytic histiocytes and atypical lymphocytes. As for the laboratory findings, leukopenia (3600+/-900 per mm(3)), anemia (hemoglobin 11.4+/-1.2 g/dL), an elevated erythrocyte sedimentation rate (44+/-18 mm/hour), and a relatively low C-reactive protein level (1.3+/-1.1 mg/dL) were noted. Eight patients received conservative therapy with antipyretics, and 3 patients were treated with prednisolone. KFD is a rare disease yet should be considered in the differential diagnosis for older children with prolonged fever and lymphadenopathy.
引用
收藏
页码:E752 / E756
页数:5
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