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*

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

1 Scopus citations

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.

Original languageEnglish
Article number6887
JournalJournal of Clinical Medicine
Volume11
Issue number23
DOIs
StatePublished - 12 2022

Bibliographical note

Publisher Copyright:
© 2022 by the authors.

Keywords

  • IgG4-related disease
  • Kimura disease
  • Taiwan
  • case report
  • overlapping features

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