論文

国際誌
2022年3月

Clinical, radiological and pathological features of idiopathic and secondary interstitial pneumonia with pleuroparenchymal fibroelastosis in patients undergoing lung transplantation.

Histopathology
  • Naoya Ikegami
  • Naoki Nakajima
  • Akihiko Yoshizawa
  • Tomohiro Handa
  • Toyofumi Chen-Yoshikawa
  • Takeshi Kubo
  • Kiminobu Tanizawa
  • Akihiro Ohsumi
  • Yoshito Yamada
  • Masatsugu Hamaji
  • Daisuke Nakajima
  • Yojiro Yutaka
  • Satona Tanaka
  • Kizuku Watanabe
  • Yoshinari Nakatsuka
  • Yuko Murase
  • Tomoko Nakanishi
  • Takafumi Niwamoto
  • Kazuo Chin
  • Hiroshi Date
  • Toyohiro Hirai
  • 全て表示

80
4
開始ページ
665
終了ページ
676
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1111/his.14595

AIMS: Idiopathic pleuroparenchymal fibroelastosis (PPFE) is a rare type of idiopathic interstitial pneumonia, and pathological PPFE is also observed in patients with secondary interstitial pneumonia. This study aimed to evaluate the pathological findings associated with radiological PPFE-like lesions and the clinical and morphological features of patients with pathological PPFE. METHODS AND RESULTS: We retrospectively reviewed the pathology of the explanted lungs from 59 lung transplant recipients with radiological PPFE-like lesions. Pathological PPFE lesions were identified in 14 patients with idiopathic disease and in 12 patients with secondary disease. Pathological PPFE was associated with previous pneumothorax, volume loss in the upper lobes, and a flattened chest. Patients with idiopathic disease and those with secondary disease with pathological PPFE had similar clinical, radiological and pathological findings, whereas fibroblastic foci were more common in patients with idiopathic disease, and patients with secondary disease more frequently showed alveolar septal thickening with elastosis or fibrosis. Post-transplantation survival did not differ between patients with idiopathic and secondary disease with pathological PPFE (log-rank; P = 0.57) and was similar between patients with idiopathic disease with pathological PPFE and those with idiopathic pulmonary fibrosis (IPF) (log-rank; P = 0.62). CONCLUSIONS: Not all patients with interstitial pneumonia with radiological PPFE-like lesions have pathological PPFE. Characteristic clinical features can suggest the presence of pathological PPFE, and idiopathic and secondary cases with pathological PPFE are similar except for fibroblastic foci in idiopathic cases and alveolar septal thickening with elastosis or fibrosis in secondary cases. Patients with pathological PPFE have a similar prognosis to those with IPF after transplantation.

リンク情報
DOI
https://doi.org/10.1111/his.14595
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/34747513
ID情報
  • DOI : 10.1111/his.14595
  • PubMed ID : 34747513

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