Bullous Vasculitis in Eosinophilic Granulomatosis with Polyangiitis: A Case Report.

ABSTRACT:

Introduction

Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare systemic vasculitis affecting small- and medium-sized vessels. It is characterized by multiorgan involvement and can lead to severe outcomes if not diagnosed promptly. Cutaneous manifestations are common and typically include palpable purpura and subcutaneous nodules. Widespread bullous vasculitis affecting areas such as the forehead and ear presents an atypical presentation. We report a case of EGPA presenting with bullous vasculitis in an unusual location.

Case presentation

A 40-year-old woman with a history of late-onset allergic rhinitis presented with a 2-week history of numbness in her right leg, along with multiple erythematous papules and vesicles, some with shallow erosions, located on the f

SUBMITTER: Phumwiriya T 

PROVIDER: S-EPMC11936433 | biostudies-literature | 2025 Jan-Dec

REPOSITORIES: biostudies-literature