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

Background 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. Case...

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Veröffentlicht in:BMC pulmonary medicine 2020-10, Vol.20 (1), p.1-264, Article 264
Hauptverfasser: Sekine, Aiko, Seo, Kohei, Matsukura, Satoshi, Sato, Masaaki, Shinozaki-Ushiku, Aya, Ogura, Takashi, Kitami, Akihiko, Kadokura, Mitsutaka, Dohi, Satoshi, Ichizuka, Kiyotake, Nagatsuka, Masaaki
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Sprache:eng
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Zusammenfassung:Background 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. Case presentation 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. Conclusion 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. Keywords: Acute exacerbation, Idiopathic pleuroparenchymal fibroelastosis, Lung transplant, Pregnancy, Case report
ISSN:1471-2466
1471-2466
DOI:10.1186/s12890-020-01308-2