Pleuroparenchymal fibroelastosis (PPFE) associated with giant cell arteritis: A coincidence or a novel phenotype?
Diagnosis
Giant cell arteritis
Pleuroparenchymal Fibroelastosis, PPFE
Pleuroparenchymal fibroelastosis
high resolution computed tomography of the chest, HRCT
light scattering spectroscopy, LSS
magnetic resonance, MRI
positron emission tomography, PET
Journal
Respiratory medicine case reports
ISSN: 2213-0071
Titre abrégé: Respir Med Case Rep
Pays: England
ID NLM: 101604463
Informations de publication
Date de publication:
2019
2019
Historique:
received:
02
03
2019
revised:
12
04
2019
accepted:
12
04
2019
entrez:
27
4
2019
pubmed:
27
4
2019
medline:
27
4
2019
Statut:
epublish
Résumé
Pleuroparenchymal fibroelastosis (PPFE) is a rare interstitial lung disease characterized by the fibrotic thickening of subpleural and parenchymal areas of the upper lobes. It may be both idiopathic or secondary to infections, interstitial lung diseases and/or drug exposure. Often PPFE patients report recurrent lower respiratory tract infections, suggesting that repeated inflammatory alterations induced by pulmonary infections may contribute to the development/progression of PPFE. Here, we report for the first time the case of a patient affected by Giant cell Arteritis with histologically proven PPFE. The lung involvement in GCA is rare and interstitial lung diseases are usually reported as an uncommon clinical manifestation of GCA. Our patient is probably the first case presenting PPFE associated with GCA and we wonder if this is a real associative disease or a coincidence perhaps, secondary to drug effects.
Identifiants
pubmed: 31024793
doi: 10.1016/j.rmcr.2019.100843
pii: S2213-0071(19)30082-6
pii: 100843
pmc: PMC6476809
doi:
Types de publication
Case Reports
Langues
eng
Pagination
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