Abstract
Kimura disease (KD) is a rare, chronic proliferative condition presenting as a subcutaneous mass predominantly located in the head and neck region; it is characterized by eosinophilia and elevated serum IgE levels. IgG4-related disease (IgG4RD) is a fibroinflammatory condition characterized by swelling in single or multiple organs and the infiltration of IgG4 plasma cells. Herein, we presented two cases. Case 1 is a 38-year-old man with a painless mass in his right postauricular region, and Case 2 is a 36-year-old man with painless lymphadenopathy in his bilateral postauricular region. After surgical excision, they showed good recovery with no relapse. Although Cases 1 and 2 shared several overlapping pathological manifestations, there were a few differences that allowed the differentiation of KD and IgG4RD.
Funder
the Center for Big Data Analytics and Statistics, Chang Gung Memorial Hospital, Linkou and Chang Gung Research Database
Reference29 articles.
1. Eosinophilic hyperplastic lymphogranuloma, comparison with Mikulicz’s disease;Chin. Med. J. (Engl.),1937
2. On the unusual granulation combined with hyperplastic changes of lymphatic tissue;Trans. Soc. Pathol. Jpn.,1948
3. Clinical, Pathological, Laboratory Characteristics, and Treatment Regimens of Kimura Disease and Their Relationships With Tumor Size and Recurrence;Front. Med.,2021
4. Kimura’s disease: Effects of age on clinical presentation;QJM Int. J. Med.,2020
5. Zhang, G., Li, X., Sun, G., Cao, Y., Gao, N., and Qi, W. (2020). Clinical analysis of Kimura’s disease in 24 cases from China. BMC Surg., 20.
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献