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A Case of Pleuroparenchymal Fibroelastosis
M. Kazui, H. Matsumoto, Y. Maezawa, G. Ohara, A. Sekine, H. Satoh
Jazyk angličtina Země Česko
Typ dokumentu kazuistiky, časopisecké články
NLK
Directory of Open Access Journals
od 2012
Medline Complete (EBSCOhost)
od 2012-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2013
PubMed
40026161
DOI
10.14712/23362936.2025.5
Knihovny.cz E-zdroje
- MeSH
- fatální výsledek MeSH
- lidé středního věku MeSH
- lidé MeSH
- plicní fibróza * diagnóza patologie MeSH
- počítačová rentgenová tomografie MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
Pleuroparenchymal fibroelastosis (PPFE) is a rare fibrotic lung disease with a poor prognosis. Some patients with PPFE have prominent lesions in one upper lobe. Due to the unilateral nature of lesions, similarities between some patients of PPFE and unilateral upper field pulmonary fibrosis (unilateral upper-PF) have been indicated. A 55-year-old man was referred to our hospital with PPFE, which had developed dyspnea 9 months previously. He had undergone resection of renal cancer 64 months prior to the onset of PPFE. He was administered the antifibrotic drug nintedanib, but passed away due to respiratory failure 43 months after the onset. What were impressive points in the clinical course of this PPFE patient was the similarity to unilateral upper-PF, including his medical history, and the poor prognosis. Although very rare, we do believe that the information on medical history and progression in this patient might provide suggestion into the treatment of future patients with a similar trajectory.
Department of Respiratory Medicine Mito Kyodo General Hospital Mito Japan
Kanagawa Cardiovascular and Respiratory Center Yokohama Japan
Citace poskytuje Crossref.org
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