Idiopathic lung fibrosis and anti myeloperoxidase glomerulonephritis: The tree that hides the forest

10Citations
Citations of this article
20Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Background: Although anti-neutrophil cytoplasmic antibodies [ANCA] are frequently found in patients diagnosed with idiopathic pulmonary fibrosis [IPF], current guidance does not recommend serologic testing for vasculitis. Case presentation: A 71-year old Caucasian male, diagnosed with IPF three years earlier, presented with rapidly progressive glomerulonephritis. ANCA were found both in current and historical sera. A kidney biopsy sample was taken, which revealed a pauci-immune glomerulonephritis, but also areas of glomerular fibrosis, hence strongly suggesting unrecognized flares of an indolent vasculitis in his past. This made the diagnosis of idiopathic pulmonary fibrosis very unlikely. Conclusion: As nephrologists, we argue that testing for ANCA should be performed on a systematic basis, at least in elderly patients, even in the absence of extra-pulmonary signs of vasculitis at presentation.

Cite

CITATION STYLE

APA

Pineton de Chambrun, M., Nunes, H., Brochériou, I., & Hertig, A. (2015). Idiopathic lung fibrosis and anti myeloperoxidase glomerulonephritis: The tree that hides the forest. BMC Pulmonary Medicine, 15(1). https://doi.org/10.1186/s12890-015-0129-5

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free