Anti-melanoma differentiation-associated gene 5 antibody associated rapidly progressive interstitial lung disease in a pediatric patient: a case report
This case demonstrates the diagnostic and therapeutic challenges in patients with rapidly progressive interstitial lung disease in the context of anti-melanoma differentiation-associated gene 5 associated juvenile dermatomyositis, who may not present with overt muscle and cutaneous features of juvenile dermatomyositis and whose lung disease can progress very rapidly. A high index of suspicion among clinicians is critical, and expedited diagnostic serology may assist with earlier diagnosis and initiation of therapy. Extracorporeal membrane oxygenation can be utilized as a bridge to diagnosis in the setting of severe refractory hypoxemic respiratory failure. However, despite aggressive treatment, the prognosis remains challenging.
Authors
- Greta Mastrangelo (ORCID: https://orcid.org/0000-0002-3455-7304)
- Haifa Mtaweh (ORCID: https://orcid.org/0000-0002-7562-549X)
- Elizaveta Limenis
- Briseida Mema (ORCID: https://orcid.org/0000-0001-9622-0304)
- Fiona Kritzinger (ORCID: https://orcid.org/0009-0004-0155-7377)
- Natalia Escobar
- Thitima Sirimontakan
Institutions
- University of Toronto (CA)
- Hospital for Sick Children (CA)
- SickKids Foundation (CA)
Publication Details
- Journal
- Journal of Medical Case Reports
- Published
- 2025-06-13
- DOI
- https://doi.org/10.1186/s13256-025-05336-6
- Citations
- 1
- Primary Topic
- Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
- Type
- article
- Field-Weighted Citation Impact
- 1.52