医学
嗜酸性粒细胞
木村病
嗜酸性粒细胞增多症
病态的
外科
血管淋巴增生伴嗜酸性粒细胞增多
头颈部
疾病
免疫球蛋白E
胃肠病学
内科学
哮喘
免疫学
抗体
作者
Yuxin Zhang,Huijie Bao,Xinyu Zhang,Fei Yang,Yang Liu,Huijuan Li,Jin Lu,Yanying Liu
出处
期刊:Clinical and Experimental Rheumatology
日期:2022-03-22
卷期号:40 (3): 532-538
被引量:4
标识
DOI:10.55563/clinexprheumatol/lahgfo
摘要
To explore the clinical characteristics, diagnosis and the therapeutic effect of Kimura's disease (KD).Clinical data of 20 patients with pathologically confirmed KD admitted to Peking University People's Hospital from June 2000 to June 2019 were analysed. A total of 20 confirmed KD patients were enrolled in the study, 18 male and 2 female, with age-onset ranging from 2 to 58 years.The masses appear as focal, painless, and immovable with an unclear boundary. The most common predilection is head-neck region (n=15, 75%). 15 patients showed peripheral blood eosinophilia. 14 of 14 patients presented with increased serum IgE level. The prominent pathological characteristic is marked lymphoid hyperplasia accompanied by various degrees of vascular hyperplasia and eosinophil infiltration. Among the 20 patients, 12 experienced recurrence of disease after treatment (surgical resection alone: 9/9; oral corticosteroids combined with immunosuppressants: 1/3; surgical resection followed by oral corticosteroids combined with immunosuppressants: 2/6).KD should be considered when the patient presents with head-neck swellings and lymphadenopathy, accompanied by an increase of IgE and eosinophil. Compared with surgery alone, combined therapy seems to be a promising treatment option to reduce the recurrence rate.
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