A Case of Interstitial Lung Disease With Apical Pleural Thickening: Idiopathic Pleuroparenchymal Fibroelastosis

Date

2014

Type:

Artículo

item.page.extent

2

item.page.accessRights

item.contributor.advisor

ORCID:

Journal Title

Journal ISSN

Volume Title

Publisher

Sociedad Española de Neumología y Cirugia Torácica

item.page.isbn

item.page.issn

item.page.issne

item.page.doiurl

item.page.other

item.page.references

Abstract

Idiopathic pleuroparenchymal fibroelastosis (IPPFE) is a very rare, recently described condition, characterised by fibrotic thickening of the pleural and subpleural parenchyma, predominantly in the upper lobes.1 Clinical manifestations and lung function tests are similar to those observed in restrictive interstitial pneumonias, and in some of the cases described, there was a history of recurrent infections, such as allergic bronchopulmonary aspergillosis or cystic fibrosis.2,3 Radiological findings include intense pleural thickening associated with signs of fibrosis, particularly in the upper lobes, with loss of volume and structural distortion, as observed in the case presented here.

Description

item.page.coverage.spatial

item.page.sponsorship

Citation

Arch Bronconeumol 2014; Vol. 50 Num.1 p:48-49

Keywords

Interstitial Lung Disease, Apical Pleural Thickening, Idiopathic Pleuroparenchymal Fibroelastosis, eldery, female, Latin America

item.page.dc.rights

item.page.dc.rights.url