A Case of Insidious Onset of Kimura Disease-associated Immunoglobulin A Nephropathy without Eosinophil Infiltration in the Renal Tissue

Authors

  • Linxin Liu Department of General Surgery, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China
  • Haoxian Gou Department of Hepatobiliary Pancreatic Surgery, School of Clinical Medicine, The First Affiliated Hospital of Chengdu Medical College, Chengdu, Sichuan, China
  • Yongfa Liu Department of General Surgery, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China
  • Shuai Hu Department of General Surgery, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China
  • Xiaoli Yang Department of General Surgery, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China
  • Bo Li Department of General Surgery, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China

DOI:

https://doi.org/10.18502/ijaai.v22i6.14649

Keywords:

Immunoglobulin A nephropathy; Infiltration of eosinophils; Kimura disease; Renal involvement

Abstract

Kimura disease (KD), also known as eosinophilic lymphogranuloma, is a rare chronic inflammatory or allergic disease. It can present with immune-related diseases such as nephrotic syndrome, asthma, and ankylosing spondylitis. In this study, we report a case of KD combined
with immunoglobulin A nephropathy that first presented as a mass in the inguinal region, followed
by recurrent renal involvement. Previous reports suggested that renal involvement caused by KD was due to direct infiltration of eosinophils; however, in this case, no eosinophil infiltration
was found in the renal tissue after renal biopsy. This observation reminds us to approach the case from an immune-related molecular perspective to investigate the exact cause of renal damage due to KD.

 

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Published

2024-01-06

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Articles