# More Than Five Years of Sustained Remission With Mepolizumab in Adolescent-Onset Eosinophilic Granulomatosis With Polyangiitis: A Case Report

**Authors:** Tomoyuki Araya, Toshiyuki Kita, Tasuku Iwabuchi, Takayuki Higashi, Ryo Hara

PMC · DOI: 10.7759/cureus.99496 · 2025-12-17

## TL;DR

A teenager with a rare autoimmune disease achieved long-term remission using a medication called mepolizumab, avoiding the need for long-term steroids.

## Contribution

This case report presents a rare adolescent-onset EGPA case with over five years of remission using mepolizumab, highlighting its steroid-sparing potential.

## Key findings

- Mepolizumab induced rapid and sustained eosinophil normalization in an adolescent with EGPA.
- The patient remained in remission for over five years without significant adverse effects.
- Mepolizumab enabled complete steroid withdrawal after three years of treatment.

## Abstract

Eosinophilic granulomatosis with polyangiitis (EGPA) typically affects middle-aged adults, and adolescent-onset disease is rare and scarcely documented in long-term real-world follow-up. We describe an 18-year-old woman with asthma who presented with fever, muscle pain, wet cough, and dyspnea. Laboratory tests showed marked leukocytosis (27,600/µL) with severe eosinophilia (17,940/µL), elevated creatine kinase, normal Krebs von den Lungen-6, elevated surfactant protein-D, markedly elevated serum immunoglobulin E, and negative proteinase 3- and myeloperoxidase-anti-neutrophil cytoplasmic antibody. Imaging revealed bilateral patchy infiltrates, and transbronchial lung biopsy demonstrated eosinophilic infiltration with granuloma formation and features of vasculitis, establishing the diagnosis of EGPA. Prednisolone 25 mg/day induced rapid improvement with normalization of eosinophils by day 12. She remained stable for nearly two years on low-dose prednisolone until asymptomatic eosinophilia recurred during tapering. Mepolizumab 300 mg every four weeks was then initiated, leading to immediate eosinophil normalization. Prednisolone was discontinued three years and 10 months after starting mepolizumab, and she has maintained remission for more than five years under continued therapy. This real-world case shows that, in adolescent-onset EGPA, where corticosteroids alone controlled disease for only two years, mepolizumab achieved sustained remission without significant adverse effects and enabled complete steroid withdrawal, underscoring its value as a long-term steroid-sparing strategy.

## Linked entities

- **Chemicals:** prednisolone (PubChem CID 5755)
- **Diseases:** eosinophilic granulomatosis with polyangiitis (MONDO:0015943), asthma (MONDO:0004979)

## Full-text entities

- **Genes:** PRTN3 (proteinase 3) [NCBI Gene 5657] {aka ACPA, AGP7, C-ANCA, CANCA, MBN, MBT}, MPO (myeloperoxidase) [NCBI Gene 4353], SFTPD (surfactant protein D) [NCBI Gene 6441] {aka COLEC7, PSP-D, SFTP4, SP-D}
- **Diseases:** vasculitis (MESH:D014657), fever (MESH:D005334), cough (MESH:D003371), granuloma (MESH:D006099), eosinophilia (MESH:D004802), asthma (MESH:D001249), dyspnea (MESH:D004417), muscle pain (MESH:D063806), leukocytosis (MESH:D007964), EGPA (MESH:D014890)
- **Chemicals:** steroid (MESH:D013256), Mepolizumab (MESH:C434107), Prednisolone (MESH:D011239)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12811164/full.md

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Source: https://tomesphere.com/paper/PMC12811164