Markedly High Peripheral Blood Eosinophilia: A Rare Manifestation of Eosinophilic Granulomatosis with Polyangiitis
Abstract
Eosinophilic granulomatosis with polyangiitis (EGPA) is a systemic necrotizing multi-system vasculitis. EGPA presents with severe eosinophilia is rare. Here we report a case of EGPA, presenting with markedly high eosinophilia with tissue infiltrates. It was successfully treated with immunosuppressive medications.
DOI: https://doi.org/10.4038/jmj.v36i2.227 | Journal eISSN: 2651-0200
Language: English
Page range: 55 - 56
Published on: Feb 7, 2025
Published by: The Jaffna Medical Association
In partnership with: Paradigm Publishing Services
© 2025 S. Sharmika, S. Rushanthini, M. Athavan, V. Jeevagan, T. Peranantharajah, published by The Jaffna Medical Association
This work is licensed under the Creative Commons Attribution 4.0 License.