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.

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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
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article

Anti-melanoma differentiation-associated gene 5 antibody associated rapidly progressive interstitial lung disease in a pediatric patient: a case report

Greta Mastrangelo, Haifa Mtaweh, Elizaveta Limenis, Briseida Mema et al.
1 citations
Journal of Medical Case Reports
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
1.52
article

Anti-melanoma differentiation-associated gene 5 antibody associated rapidly progressive interstitial lung disease in a pediatric patient: a case report

Greta Mastrangelo, Haifa Mtaweh, Elizaveta Limenis, Briseida Mema, Fiona Kritzinger, Natalia Escobar, Thitima Sirimontakan
article en
1 citations

Abstract

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.

Journal of Medical Case ReportsVol. 19(1)
University of Toronto (CA), Hospital for Sick Children (CA), SickKids Foundation (CA)
Openalex Percentile: Top 17%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
1.52
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Anti-melanoma differentiation-associated gene 5 antibody associated rapidly progressive interstitial lung disease in a pediatric patient: a case report — Greta Mastrangelo, Haifa Mtaweh, et al. · Journal of Medical Case Reports (2025) | TGRS Research Map | TGRS