Kimura’s disease an unusual cause of lymphadenopathy in a nephrotic syndrome child

Nefrotik sendromlu bir çocukta lenfadenopatinin olağandışı nedeni olarak Kimura hastalığı


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Authors

  • Chenthilnathan Periasamy Universiti Sains Malaysia, School of Medical Sciences, Department of Otolaryngology-Head and Neck Surgery, Kubang Kerian, Kelantan
  • Norzaliana Zawawi Universiti Sains Malaysia, School of Medical Sciences, Department of Pathology, Kubang Kerian, Kelantan
  • Md Salzihan Md Salleh Universiti Sains Malaysia, School of Medical Sciences, Department of Pathology, Kubang Kerian, Kelantan
  • Baharudin Abdullah Universiti Sains Malaysia, School of Medical Sciences, Department of Otolaryngology-Head and Neck Surgery, Kubang Kerian, Kelantan

DOI:

https://doi.org/10.5455/GMJ-30-2012-71

Keywords:

Immunoglobulin E, Kimura’s disease, lymphadenopathy, nephrotic syndrome, peripheral eosinophilia

Abstract

Kimura’s disease is a rare, benign, chronic inflammatory disorder of unknown etiology which is endemic in Orientals. The disease is characterized by a triad of painless subcutaneous nodule in the head and neck region, blood eosinophilia and elevated serum immunoglobulin E (IgE) levels. Kimura’s disease has various synonyms such as eosinophilic lymphogranuloma, inflammatory angiomatous nodule and atypical pyogenic granuloma. Renal pathology such as nephrotic syndrome has been found to be associated with Kimura’s disease which states a common etiopathogenesis between renal lesion and Kimura’s disease. We present an eleven years old Malay boy with recurrent nephrotic syndrome presented with left post auricular swelling. The diagnosis was based on the characteristic histopathology findings after surgical biopsy as Kimura’s disease.

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References

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Published

2023-05-02

How to Cite

Periasamy, C., Zawawi, N., Md Salleh, M. S., & Abdullah, B. (2023). Kimura’s disease an unusual cause of lymphadenopathy in a nephrotic syndrome child: Nefrotik sendromlu bir çocukta lenfadenopatinin olağandışı nedeni olarak Kimura hastalığı. European Journal of Therapeutics, 18(2), 101–105. https://doi.org/10.5455/GMJ-30-2012-71

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Section

Case Reports