4.6 Article

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

Journal

HISTOPATHOLOGY
Volume 80, Issue 4, Pages 665-676

Publisher

WILEY
DOI: 10.1111/his.14595

Keywords

haematopoietic stem cell transplantation; interstitial lung disease; lung transplantation; pleuroparenchymal fibroelastosis

Funding

  1. Japan Society for the Promotion of Science [20K08925]
  2. Japan Society for the Promotion of Science KAKENHI [19K08648]
  3. Grants-in-Aid for Scientific Research [19K08648, 20K08925] Funding Source: KAKEN

Ask authors/readers for more resources

This study evaluated the pathological findings associated with radiological PPFE-like lesions and the clinical and morphological features of patients with pathological PPFE. The results showed that pathological PPFE was related to 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. However, fibroblastic foci were more common in idiopathic cases and alveolar septal thickening with elastosis or fibrosis were more common in secondary cases. The post-transplantation survival of patients with pathological PPFE was similar to those with idiopathic pulmonary fibrosis (IPF).
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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available