Home
World Journal of Biology Pharmacy and Health Sciences
ISSN Approved | International, Peer reviewed, Referred, Open access Journal

Main navigation

  • Home
    • Journal Information
    • Abstracting and Indexing
    • Editorial Board Members
    • Reviewer Panel
    • Journal Policies
    • WJBPHS CrossMark Policy
    • Publication Ethics
    • Current Issue
    • Issue in Progress
    • Past Issues
    • Instructions for Authors
    • Article processing fee
    • Track Manuscript Status
    • Get Publication Certificate
    • Become a Reviewer panel member
    • Join as Editorial Board Member
  • Contact us
  • Downloads

ISSN Approved Journal | | IMPACT FACTOR 8.16 | | eISSN: 2582-5542 | |  Free Crossref DOI 

Fast Publication within 2 days | | Low Article Processing Charges | | Peer Reviewed and Referred Journal

Research and review articles are invited for publication in September 2026 (Volume 27, Issue 3) Submit Paper

Kimura disease presenting with isolated axillary lymphadenopathy and eosinophilia in a young female: A case report and review of diagnostic and management considerations

Breadcrumb

  • Home
  • Kimura disease presenting with isolated axillary lymphadenopathy and eosinophilia in a young female: A case report and review of diagnostic and management considerations

Talina Fuentes 1, Cindy Almaraz 2, Marcos Domínguez 3, Rikki Johnson 1, Jessica Jahoda 4, 5 and Mohamed Aziz 5, *

1 American University of the Caribbean, AUC, St. Maarten.
2 Ross University School of Medicine, Barbados.
3 Universidad Iberoamericana (UNIBE), Santo Domingo, Dominican Republic.
4 Memorial Healthcare System, Pembroke Pines, FL, USA.
5 Research Writing and Publication (RWP), LLC, NY, USA.

Case Report

World Journal of Biology Pharmacy and Health Sciences, 2026, 27(01), 084-090

Article DOI: 10.30574/wjbphs.2026.27.1.0385

DOI url: https://doi.org/10.30574/wjbphs.2026.27.1.0385

Received on 06 June 2026; revised on 11 July 2026; accepted on 14 July 2026

Kimura disease (KD) is a rare, benign, chronic inflammatory disorder that predominantly affects young Asian men in the head and neck region. Presentation as solitary axillary lymphadenopathy in a female patient is highly uncommon, and diagnostically challenging. Our case follows a 32-year-old Asian woman with a six-month history of erythematous forearm rash, nocturnal pruritus, and progressively enlarging, painless left axillary swelling. Initial assessment revealed peripheral eosinophilia and markedly elevated serum IgE levels. Contrast-enhanced imaging demonstrated isolated left axillary lymphadenopathy without evidence of organomegaly, systemic nodal involvement, or mediastinal extension. Histopathological analysis identified microabscesses, extensive eosinophilic infiltration, and florid germinal center hyperplasia. Molecular and immunohistochemical (IHC) studies confirmed a polyclonal lymphoid pattern, excluding viral etiologies, IgG4-related disease, and lymphoma. 
Management with complete surgical excision was performed following multidisciplinary tumor board review, resulting in symptom resolution and normalization of laboratory findings. Sequential multifocal recurrences, initially in the right cervical region at fourteen months and contralateral axilla, required a gradual transition from systemic corticosteroids to low-dose cyclosporine. Sustained remission was maintained after 18 months of follow-up, with stable renal function throughout the disease course. 
This case contributes to the limited literature on atypical presentations of Kimura disease, underscores the importance of considering this diagnosis in cases of unexplained eosinophilic lymphadenopathy irrespective of anatomical location or sex, and highlights the chronic, relapsing-remitting nature of the disease, which necessitates individualized, multidisciplinary long-term management.

Kimura disease; Eosinophilic lymphadenopathy; Chronic inflammatory disorder; Peripheral eosinophilia

https://wjbphs.com/sites/default/files/fulltext_pdf/WJBPHS-2026-0385.pdf

Get Your e Certificate of Publication using below link

Download Certificate

Preview Article PDF

Talina Fuentes, Cindy Almaraz, Marcos Domínguez, Rikki Johnson, Jessica Jahoda and Mohamed Aziz. Kimura disease presenting with isolated axillary lymphadenopathy and eosinophilia in a young female: A case report and review of diagnostic and management considerations. World Journal of Biology Pharmacy and Health Sciences, 2026, 27(01), 084-090. Article DOI: https://doi.org/10.30574/wjbphs.2026.27.1.0385

Get Certificates

Get Publication Certificate

Download LoA

Check Corssref DOI details

Issue details

Issue Cover Page

Editorial Board

Table of content


Copyright © Author(s). All rights reserved. This article is published under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0), which permits use, sharing, adaptation, distribution, and reproduction in any medium or format, as long as appropriate credit is given to the original author(s) and source, a link to the license is provided, and any changes made are indicated.


Copyright © 2026 World Journal of Biology Pharmacy and Health Sciences (WJBPHS) - All rights reserved

Developed & Designed by VS Infosolution