Back to Search Start Over

A case report of idiopathic pleuroparenchymal fibroelastosis with severe respiratory failure in pregnancy.

Authors :
Sekine, Aiko
Seo, Kohei
Matsukura, Satoshi
Sato, Masaaki
Shinozaki-Ushiku, Aya
Ogura, Takashi
Kitami, Akihiko
Kadokura, Mitsutaka
Dohi, Satoshi
Ichizuka, Kiyotake
Nagatsuka, Masaaki
Source :
BMC Pulmonary Medicine; 10/14/2020, Vol. 20 Issue 1, p1-5, 5p
Publication Year :
2020

Abstract

<bold>Background: </bold>Idiopathic pleuroparenchymal fibroelastosis (IPPFE) is a rare lung disease that manifests as parenchymal fibrosis of the upper lung lobe and pleura. There have been no reports of IPPFE complicating pregnancy. Here, we report a case of IPPFE that deteriorated rapidly during pregnancy.<bold>Case Presentation: </bold>A 29-year-old woman presented with dyspnea and dry cough at 19 weeks of gestation. IPPFE with acute exacerbation was suspected on chest computed tomography (CT). Despite steroid treatment, her condition progressed. A cesarean section was performed at 28 weeks of gestation. On postoperative day 26, she underwent living-donor lung transplantation. She was discharged a year after transplantation.<bold>Conclusion: </bold>Our experience suggested that when pregnancy is complicated by PPFE, the disease may deteriorate rapidly. In this case, even though IPPFE with acute exacerbation was diagnosed during pregnancy, live birth was achieved, and the mother survived after lung transplantation. Lung transplantation should be considered in these patients because, once advanced, pulmonary lesions may be irreversible. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14712466
Volume :
20
Issue :
1
Database :
Complementary Index
Journal :
BMC Pulmonary Medicine
Publication Type :
Academic Journal
Accession number :
146431345
Full Text :
https://doi.org/10.1186/s12890-020-01308-2