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Comparison of Clinical Manifestations and Pathology between Kimura Disease and IgG4-Related Disease: A Report of Two Cases and Literature Review

  • Sing Ya Chang
  • , Chih Chun Lee
  • , Ming Ling Chang
  • , Wen Chieh Teng
  • , Chao Yang Hsiao
  • , Han Hua Yu
  • , Meng Ju Hsieh
  • , Tien Ming Chan*
  • *此作品的通信作者
  • Chang Gung University
  • Chang Gung Memorial Hospital

研究成果: 期刊稿件文章同行評審

2 引文 斯高帕斯(Scopus)

摘要

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.

原文英語
文章編號6887
期刊Journal of Clinical Medicine
11
發行號23
DOIs
出版狀態已出版 - 12 2022

文獻附註

Publisher Copyright:
© 2022 by the authors.

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