Eosinophilic Granulomatosis with Polyangiitis presenting as Necrotizing Glomerulonephritis

Authors

  • Uzma Anwar Resident - Department of Medicine, Khyber Teaching Hospital, Peshawar ";}
  • Maria Tahir Resident - Department of Nephrology, Khyber Teaching Hospital, Peshawar
  • Nida Wali Khan Resident - Department of Medicine, Khyber Teaching Hospital, Peshawar
  • Tayyaba Tahir Medical Officer, Jinnah Teaching Hospital, Peshawar
  • Javed Ali Resident, Department of Medicine, Khyber Teaching Hospital, Peshawar

Keywords:

EGPA (Eosinophilic Granulomatosis with Polyangiitis), Glomerulonephritis, ANCA

Abstract

Eosinophilic Granulomatosis with Polyangiitis (EGPA) previously known as Churg-Strauss syndrome, belongs to a group of diseases with features of necrotizing vasculitis of small and medium-sized arteries. Its distinctive features include rhinosinusitis, asthma, prominent blood eosinophilia. (1)

We hereby report a case of a 70-year-old male patient with a history of newly diagnosed hypertension and asthma, presented to us with bilateral lower limb edema. His investigations showed proteinuria of 1.7g/24hours and p-ANCA positive. His renal biopsy was done which was reported as Focal Necrotizing Glomerulonephritis.

Published

2025-11-19

How to Cite

Anwar, U., Tahir, M., Khan, N. W., Tahir, T., & Ali, J. (2025). Eosinophilic Granulomatosis with Polyangiitis presenting as Necrotizing Glomerulonephritis. Journal of Medical Sciences, 31(4). Retrieved from https://jmedsci.com/Jmedsci/article/view/1770

Issue

Vol. 31 No. 4 (2023): Journal of Medical Sciences

Section

Case Report

License

Copyright (c) 2023 Uzma Anwar, Maria Tahir, Nida Wali Khan, Tayyaba Tahir, Javed Ali

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