Radiologic pleuroparenchymal fibroelastosis-like lesion in connective tissue disease-related interstitial lung disease

Radiologic pleuroparenchymal fibroelastosis (PPFE)-like lesion including pulmonary apical cap can be occasionally observed in clinical settings. However, the significance of radiologic PPFE-like lesion is unclear in connective tissue disease (CTD)-related interstitial lung disease (ILD). A total of...

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Veröffentlicht in:PloS one 2017-06, Vol.12 (6), p.e0180283-e0180283
Hauptverfasser: Enomoto, Yasunori, Nakamura, Yutaro, Colby, Thomas V, Johkoh, Takeshi, Sumikawa, Hiromitsu, Nishimoto, Koji, Yoshimura, Katsuhiro, Matsushima, Sayomi, Oyama, Yoshiyuki, Hozumi, Hironao, Kono, Masato, Fujisawa, Tomoyuki, Enomoto, Noriyuki, Inui, Naoki, Iwashita, Toshihide, Suda, Takafumi
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container_start_page e0180283
container_title PloS one
container_volume 12
creator Enomoto, Yasunori
Nakamura, Yutaro
Colby, Thomas V
Johkoh, Takeshi
Sumikawa, Hiromitsu
Nishimoto, Koji
Yoshimura, Katsuhiro
Matsushima, Sayomi
Oyama, Yoshiyuki
Hozumi, Hironao
Kono, Masato
Fujisawa, Tomoyuki
Enomoto, Noriyuki
Inui, Naoki
Iwashita, Toshihide
Suda, Takafumi
description Radiologic pleuroparenchymal fibroelastosis (PPFE)-like lesion including pulmonary apical cap can be occasionally observed in clinical settings. However, the significance of radiologic PPFE-like lesion is unclear in connective tissue disease (CTD)-related interstitial lung disease (ILD). A total of 113 patients with CTD-related ILD were enrolled and assessed for radiologic PPFE-like lesion, which was defined as bilateral, upper lobe, and subpleural dense consolidations with or without pleural thickening on chest high-resolution computed tomography. The clinical, radiologic, and pathologic characteristics were evaluated. Radiologic PPFE-like lesion was found in 21 patients (19%) and were relatively frequent in those with systemic sclerosis (6/14: 43%) and primary Sjögren's syndrome (4/14: 29%). Patients with PPFE-like lesion were significantly older, had lower body mass index, higher ratio of residual volume to total lung capacity, and higher complication rate of pneumothorax and/or pneumomediastinum than those without. Twelve of the 21 patients were diagnosed radiologically as usual interstitial pneumonia (UIP) or possible UIP pattern. Two of three patients who underwent surgical lung biopsy of the upper lobes showed UIP on histopathology. Another patient was confirmed to have upper lobe PPFE on autopsy. During the clinical course, progression of the radiologic PPFE-like lesions was observed in 13 of 21 patients. Six patients died (mortality rate: 29%) and their PPFE-like lesions were commonly progressive. In the total cohort, our multivariate analysis identified the presence of PPFE-like lesion as a significant risk factor for respiratory death (hazard ratio: 4.10, 95% confidence interval: 1.33-12.65, p = 0.01). In patients with CTD-related ILD, radiologic PPFE-like lesion, which may present as not only PPFE but also apical cap and upper lobe subpleural fibrosis commonly due to UIP, was not uncommon and was associated with poor prognosis. Clinicians should be cautious with this radiologic finding, particularly when it is progressive.
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However, the significance of radiologic PPFE-like lesion is unclear in connective tissue disease (CTD)-related interstitial lung disease (ILD). A total of 113 patients with CTD-related ILD were enrolled and assessed for radiologic PPFE-like lesion, which was defined as bilateral, upper lobe, and subpleural dense consolidations with or without pleural thickening on chest high-resolution computed tomography. The clinical, radiologic, and pathologic characteristics were evaluated. Radiologic PPFE-like lesion was found in 21 patients (19%) and were relatively frequent in those with systemic sclerosis (6/14: 43%) and primary Sjögren's syndrome (4/14: 29%). Patients with PPFE-like lesion were significantly older, had lower body mass index, higher ratio of residual volume to total lung capacity, and higher complication rate of pneumothorax and/or pneumomediastinum than those without. Twelve of the 21 patients were diagnosed radiologically as usual interstitial pneumonia (UIP) or possible UIP pattern. Two of three patients who underwent surgical lung biopsy of the upper lobes showed UIP on histopathology. Another patient was confirmed to have upper lobe PPFE on autopsy. During the clinical course, progression of the radiologic PPFE-like lesions was observed in 13 of 21 patients. Six patients died (mortality rate: 29%) and their PPFE-like lesions were commonly progressive. In the total cohort, our multivariate analysis identified the presence of PPFE-like lesion as a significant risk factor for respiratory death (hazard ratio: 4.10, 95% confidence interval: 1.33-12.65, p = 0.01). In patients with CTD-related ILD, radiologic PPFE-like lesion, which may present as not only PPFE but also apical cap and upper lobe subpleural fibrosis commonly due to UIP, was not uncommon and was associated with poor prognosis. Clinicians should be cautious with this radiologic finding, particularly when it is progressive.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0180283</identifier><identifier>PMID: 28666014</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Aged ; Autopsies ; Autopsy ; Biology and Life Sciences ; Biopsy ; Body mass ; Body mass index ; Care and treatment ; CAT scans ; Computed tomography ; Confidence intervals ; Connective tissue diseases ; Connective Tissue Diseases - complications ; Connective Tissue Diseases - diagnostic imaging ; Connective Tissue Diseases - pathology ; Connective tissues ; Consolidation ; Death ; Female ; Fibrosis ; High resolution ; Histopathology ; Humans ; Infections ; Influence ; Internal medicine ; Interstitial lung diseases ; Laboratories ; Lesions ; Lobes ; Lung diseases ; Lung Diseases, Interstitial - complications ; Lung Diseases, Interstitial - diagnostic imaging ; Lung Diseases, Interstitial - pathology ; Male ; Medical prognosis ; Medicine ; Medicine and Health Sciences ; Middle Aged ; Multivariate analysis ; Obstructive lung disease ; Pathology ; Patients ; Physicians ; Pleural Diseases - complications ; Pleural Diseases - diagnostic imaging ; Pleural Diseases - pathology ; Pneumonia ; Pneumothorax ; Prognosis ; Pulmonary fibrosis ; Pulmonary Fibrosis - complications ; Pulmonary Fibrosis - diagnostic imaging ; Pulmonary Fibrosis - pathology ; Retrospective Studies ; Risk factors ; Scleroderma ; Sjogren's syndrome ; Surgery ; Systemic sclerosis ; Thickening ; Tomography ; Tomography, X-Ray Computed</subject><ispartof>PloS one, 2017-06, Vol.12 (6), p.e0180283-e0180283</ispartof><rights>COPYRIGHT 2017 Public Library of Science</rights><rights>2017 Enomoto et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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However, the significance of radiologic PPFE-like lesion is unclear in connective tissue disease (CTD)-related interstitial lung disease (ILD). A total of 113 patients with CTD-related ILD were enrolled and assessed for radiologic PPFE-like lesion, which was defined as bilateral, upper lobe, and subpleural dense consolidations with or without pleural thickening on chest high-resolution computed tomography. The clinical, radiologic, and pathologic characteristics were evaluated. Radiologic PPFE-like lesion was found in 21 patients (19%) and were relatively frequent in those with systemic sclerosis (6/14: 43%) and primary Sjögren's syndrome (4/14: 29%). Patients with PPFE-like lesion were significantly older, had lower body mass index, higher ratio of residual volume to total lung capacity, and higher complication rate of pneumothorax and/or pneumomediastinum than those without. Twelve of the 21 patients were diagnosed radiologically as usual interstitial pneumonia (UIP) or possible UIP pattern. Two of three patients who underwent surgical lung biopsy of the upper lobes showed UIP on histopathology. Another patient was confirmed to have upper lobe PPFE on autopsy. During the clinical course, progression of the radiologic PPFE-like lesions was observed in 13 of 21 patients. Six patients died (mortality rate: 29%) and their PPFE-like lesions were commonly progressive. In the total cohort, our multivariate analysis identified the presence of PPFE-like lesion as a significant risk factor for respiratory death (hazard ratio: 4.10, 95% confidence interval: 1.33-12.65, p = 0.01). In patients with CTD-related ILD, radiologic PPFE-like lesion, which may present as not only PPFE but also apical cap and upper lobe subpleural fibrosis commonly due to UIP, was not uncommon and was associated with poor prognosis. Clinicians should be cautious with this radiologic finding, particularly when it is progressive.</description><subject>Aged</subject><subject>Autopsies</subject><subject>Autopsy</subject><subject>Biology and Life Sciences</subject><subject>Biopsy</subject><subject>Body mass</subject><subject>Body mass index</subject><subject>Care and treatment</subject><subject>CAT scans</subject><subject>Computed tomography</subject><subject>Confidence intervals</subject><subject>Connective tissue diseases</subject><subject>Connective Tissue Diseases - complications</subject><subject>Connective Tissue Diseases - diagnostic imaging</subject><subject>Connective Tissue Diseases - pathology</subject><subject>Connective tissues</subject><subject>Consolidation</subject><subject>Death</subject><subject>Female</subject><subject>Fibrosis</subject><subject>High resolution</subject><subject>Histopathology</subject><subject>Humans</subject><subject>Infections</subject><subject>Influence</subject><subject>Internal medicine</subject><subject>Interstitial lung diseases</subject><subject>Laboratories</subject><subject>Lesions</subject><subject>Lobes</subject><subject>Lung diseases</subject><subject>Lung Diseases, Interstitial - complications</subject><subject>Lung Diseases, Interstitial - diagnostic imaging</subject><subject>Lung Diseases, Interstitial - pathology</subject><subject>Male</subject><subject>Medical prognosis</subject><subject>Medicine</subject><subject>Medicine and Health Sciences</subject><subject>Middle Aged</subject><subject>Multivariate analysis</subject><subject>Obstructive lung disease</subject><subject>Pathology</subject><subject>Patients</subject><subject>Physicians</subject><subject>Pleural Diseases - complications</subject><subject>Pleural Diseases - diagnostic imaging</subject><subject>Pleural Diseases - pathology</subject><subject>Pneumonia</subject><subject>Pneumothorax</subject><subject>Prognosis</subject><subject>Pulmonary fibrosis</subject><subject>Pulmonary Fibrosis - complications</subject><subject>Pulmonary Fibrosis - diagnostic imaging</subject><subject>Pulmonary Fibrosis - pathology</subject><subject>Retrospective Studies</subject><subject>Risk factors</subject><subject>Scleroderma</subject><subject>Sjogren's syndrome</subject><subject>Surgery</subject><subject>Systemic sclerosis</subject><subject>Thickening</subject><subject>Tomography</subject><subject>Tomography, X-Ray 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Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Enomoto, Yasunori</au><au>Nakamura, Yutaro</au><au>Colby, Thomas V</au><au>Johkoh, Takeshi</au><au>Sumikawa, Hiromitsu</au><au>Nishimoto, Koji</au><au>Yoshimura, Katsuhiro</au><au>Matsushima, Sayomi</au><au>Oyama, Yoshiyuki</au><au>Hozumi, Hironao</au><au>Kono, Masato</au><au>Fujisawa, Tomoyuki</au><au>Enomoto, Noriyuki</au><au>Inui, Naoki</au><au>Iwashita, Toshihide</au><au>Suda, Takafumi</au><au>Kuwana, Masataka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Radiologic pleuroparenchymal fibroelastosis-like lesion in connective tissue disease-related interstitial lung disease</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2017-06-30</date><risdate>2017</risdate><volume>12</volume><issue>6</issue><spage>e0180283</spage><epage>e0180283</epage><pages>e0180283-e0180283</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Radiologic pleuroparenchymal fibroelastosis (PPFE)-like lesion including pulmonary apical cap can be occasionally observed in clinical settings. However, the significance of radiologic PPFE-like lesion is unclear in connective tissue disease (CTD)-related interstitial lung disease (ILD). A total of 113 patients with CTD-related ILD were enrolled and assessed for radiologic PPFE-like lesion, which was defined as bilateral, upper lobe, and subpleural dense consolidations with or without pleural thickening on chest high-resolution computed tomography. The clinical, radiologic, and pathologic characteristics were evaluated. Radiologic PPFE-like lesion was found in 21 patients (19%) and were relatively frequent in those with systemic sclerosis (6/14: 43%) and primary Sjögren's syndrome (4/14: 29%). Patients with PPFE-like lesion were significantly older, had lower body mass index, higher ratio of residual volume to total lung capacity, and higher complication rate of pneumothorax and/or pneumomediastinum than those without. Twelve of the 21 patients were diagnosed radiologically as usual interstitial pneumonia (UIP) or possible UIP pattern. Two of three patients who underwent surgical lung biopsy of the upper lobes showed UIP on histopathology. Another patient was confirmed to have upper lobe PPFE on autopsy. During the clinical course, progression of the radiologic PPFE-like lesions was observed in 13 of 21 patients. Six patients died (mortality rate: 29%) and their PPFE-like lesions were commonly progressive. In the total cohort, our multivariate analysis identified the presence of PPFE-like lesion as a significant risk factor for respiratory death (hazard ratio: 4.10, 95% confidence interval: 1.33-12.65, p = 0.01). In patients with CTD-related ILD, radiologic PPFE-like lesion, which may present as not only PPFE but also apical cap and upper lobe subpleural fibrosis commonly due to UIP, was not uncommon and was associated with poor prognosis. Clinicians should be cautious with this radiologic finding, particularly when it is progressive.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>28666014</pmid><doi>10.1371/journal.pone.0180283</doi><tpages>e0180283</tpages><orcidid>https://orcid.org/0000-0003-1920-4268</orcidid><oa>free_for_read</oa></addata></record>
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1932-6203
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source MEDLINE; DOAJ Directory of Open Access Journals; Public Library of Science (PLoS) Journals Open Access; EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry
subjects Aged
Autopsies
Autopsy
Biology and Life Sciences
Biopsy
Body mass
Body mass index
Care and treatment
CAT scans
Computed tomography
Confidence intervals
Connective tissue diseases
Connective Tissue Diseases - complications
Connective Tissue Diseases - diagnostic imaging
Connective Tissue Diseases - pathology
Connective tissues
Consolidation
Death
Female
Fibrosis
High resolution
Histopathology
Humans
Infections
Influence
Internal medicine
Interstitial lung diseases
Laboratories
Lesions
Lobes
Lung diseases
Lung Diseases, Interstitial - complications
Lung Diseases, Interstitial - diagnostic imaging
Lung Diseases, Interstitial - pathology
Male
Medical prognosis
Medicine
Medicine and Health Sciences
Middle Aged
Multivariate analysis
Obstructive lung disease
Pathology
Patients
Physicians
Pleural Diseases - complications
Pleural Diseases - diagnostic imaging
Pleural Diseases - pathology
Pneumonia
Pneumothorax
Prognosis
Pulmonary fibrosis
Pulmonary Fibrosis - complications
Pulmonary Fibrosis - diagnostic imaging
Pulmonary Fibrosis - pathology
Retrospective Studies
Risk factors
Scleroderma
Sjogren's syndrome
Surgery
Systemic sclerosis
Thickening
Tomography
Tomography, X-Ray Computed
title Radiologic pleuroparenchymal fibroelastosis-like lesion in connective tissue disease-related interstitial lung disease
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