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Markedly High Peripheral Blood Eosinophilia: A Rare Manifestation of Eosinophilic Granulomatosis with Polyangiitis

Year: 2025

Type: article

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.

Source: Jaffna Medical Journal

DOI: 10.4038/jmj.v36i2.227

Authors: S. Sharmika, S. Rushanthini, M. Athavan, V. Jeevagan, T. Peranantharajah

Language: English

Topic: Vasculitis and related conditions

Subfield: Pulmonary and Respiratory Medicine

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: diamond

OpenAlex ID: W4407239680

FWCI:

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