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

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.

Authors

Publication Details

Journal
Jaffna Medical Journal
Published
2025-02-07
DOI
https://doi.org/10.4038/jmj.v36i2.227
Primary Topic
Eosinophilic Disorders and Syndromes
Type
article
Field-Weighted Citation Impact
0.00
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article

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

S. Sharmika, S. Rushanthini, V. Jeevagan, T. Peranantharajah et al.
Jaffna Medical Journal
Eosinophilic Disorders and Syndromes
article

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

S. Sharmika, S. Rushanthini, V. Jeevagan, T. Peranantharajah, M. Athavan
article en

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.

Jaffna Medical JournalVol. 36(2)
Openalex Percentile: Top 97%
Eosinophilic Disorders and Syndromes
DOIOpen Access PDFOpenAlex
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Markedly High Peripheral Blood Eosinophilia: A Rare Manifestation of Eosinophilic Granulomatosis with Polyangiitis — S. Sharmika, S. Rushanthini, et al. · Jaffna Medical Journal (2025) | TGRS Research Map | TGRS