Microscopic polyangiitis presenting as idiopathic pulmonary fibrosis

The most detectable form of pulmonary fibrosis in MPA (microscopic polyangiitis) is UIP (usual interstitial pneumonia), occurring in 48 % of MPA patients with pulmonary fibrosis. In some cases, ILD (interstitial lung disease) is the initial clinical manifestation of MPA (22 % of cases). Here, we des...

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Bibliografiska uppgifter

Huvudupphov:	Brittany Duchene
Materialtyp:	Artigo
Språk:	Inglês
Utgiven:	Elsevier 2024-01-01
Serie:	Respiratory Medicine Case Reports
Ämnen:	Microscopic polyangiitis Idiopathic pulmonary fibrosis Interstitial lung disease ANCA-Associated vasculitis Diffuse alveolar hemorrhage
Länkar:	http://www.sciencedirect.com/science/article/pii/S221300712400145X
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