ArticleInternal medicine (Tokyo, Japan)2020
An Autopsy Case of Idiopathic Pleuroparenchymal Fibroelastosis with Left Vocal Cord Paralysis and a Rapid Deterioration without an Acute Exacerbation.
Article in Internal medicine (Tokyo, Japan), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
3 citing papers in PubMed, 7 citations in OpenAlex.
- A middle-aged man with dyspnea and hoarseness: an unusual case of vocal cord paralysis.BMC pulmonary medicine · 2025Article
- Left vocal cord paralysis in a patient with pleuroparenchymal fibroelastosis.Oxford medical case reports · 2023Article
- The pathogenesis and pathology of idiopathic pleuroparenchymal fibroelastosis.Histology and histopathology · 2021Review
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Authors and funding
7 authors at 1 institution in 1 country.
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Abstract
Idiopathic pleuroparenchymal fibroelastosis (IPPFE) is a generally slow-progressing rare disorder of unknown etiology. The direct cause of death in cases of IPPFE is rarely investigated. We experienced an autopsy case of a Japanese man with IPPFE and found aspiration pneumonia to be the major trigger of death. The individual had left vocal cord paralysis at admission, which may have contributed to aspiration pneumonia, and which probably was affected by the fibrous adhesion of the left apex of the chest wall resulting from IPPFE. The prevention of aspiration pneumonia is important for maintaining the respiratory function, especially in IPPFE patients with repeated pneumothorax.
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