# The clinical and pathological features of Kimura disease in pediatric patients

**Authors:** Lili Liu, Wen Zhang, Minjie Huang, Kaiji Li, Li’ou Zhu, Liqin Ke, Juan Huang, Ying Wu

PMC · DOI: 10.3389/fmed.2024.1352206 · Frontiers in Medicine · 2024-04-25

## TL;DR

This study examines the clinical and pathological features of Kimura disease in children, highlighting the role of IgE in diagnosis.

## Contribution

The study provides new insights into the diagnostic significance of IgE in pediatric Kimura disease cases.

## Key findings

- Eighty percent of pediatric patients showed eosinophilia and 40% had elevated IgE levels.
- Histopathological features included eosinophilic infiltrates and IgE deposition in follicles.
- No recurrence was observed after surgical excision in all patients.

## Abstract

Kimura disease is characterized by inflammation, with its underlying causes remaining uncertain. There is a lack of comprehensive and systematic research on the pathology of this condition in pediatric patients. Our objective is to study the clinical and pathological attributes of Kimura disease in pediatric patients and investigate the potential diagnostic significance of immunoglobulin E (IgE) in this context.

Clinical and laboratory information, pathological characteristics, and follow-up data were correlated to examine the distinctive features. Immunohistochemistry, acid-fast staining, and molecular assay were used to identify the presence of IgE and pathogens.

We conducted an analysis of five cases of Kimura disease in pediatric patients at our hospital. The patients’ ages ranged from 5 years and 7 months to 14 years and 2 months, with 4 (80%) being male. The most common site was the head and neck region, particularly the postauricular subcutaneous area. Eosinophilia was observed in four patients (80%), and two patients (40%) had elevated serum immunoglobulin E (IgE) levels. Histopathological changes included eosinophilic infiltrates, follicular hyperplasia, and the proliferation of postcapillary venules. Immunohistochemical results supported the reactive nature of the lymphoid process and IgE deposition in the follicle, while no specific pathogens were discovered by special staining. All patients underwent surgical excision, and none experienced recurrence in their original location.

Children with Kimura disease show distinct eosinophilic and IgE alterations in both laboratory findings and pathological features. The application of immunohistochemical staining of IgE could serve as a promising marker for diagnosing Kimura disease.

## Linked entities

- **Proteins:** IGHE (immunoglobulin heavy constant epsilon)
- **Diseases:** Kimura disease (MONDO:0018830)

## Full-text entities

- **Genes:** IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}
- **Diseases:** Kimura disease (MESH:D000082242), hyperplasia (MESH:D006965), Eosinophilia (MESH:D004802), inflammation (MESH:D007249)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11079225/full.md

## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC11079225/full.md

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Source: https://tomesphere.com/paper/PMC11079225