Eosinophilic Granulomatosis with Polyangiitis - description of a pediatric patient with severe disease

• Published in: ARP rheumatology Vol. 2; no. 2; p. 160
• Main Authors: Barbosa Rodrigues, Ana, Oliveira-Ramos, Filipa, Ferreira, Rosário, Camilo, Cristina, Oliveira, Tiago, Costa-Reis, Patrícia
• Format: Journal Article
• Language: English
• Published: Portugal 01.04.2023
• ISSN: 2795-4552

Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare vasculitis of small and medium sized blood vessels. Thirteen-year-old male, with history of rhinitis and asthma, who presented to the emergency room with one week of asthenia, arthralgias and myalgias and two days of fever. A diffuse petechial rash, palpable purpura and polyarthritis were detected on examination. Leukocytosis (34990/μL) with eosinophilia (66%) and elevated C-reactive protein were identified. The patient was admitted and ceftriaxone and doxycycline were started. The clinical status deteriorated in the following days. The patient developed myopericarditis, bilateral pulmonary infiltrates and pleural effusion, requiring mechanical ventilation and aminergic support. Non-clonal eosinophils were detected on the bone marrow aspiration and the skin biopsy showed leukocytoclastic vasculitis with eosinophils. Antineutrophil cytoplasmic antibodies and genetic analysis for hypereosinophilic syndrome mutations were negative. After treatment with methylprednisolone for three days a fast clinical, laboratory and radiological improvement occurred. The patient started azatiophrine and reduced steroids progressively. No relapses occurred since diagnosis five years ago. Clinical suspicion and early treatment of EGPA are crucial to improve prognosis.