Idiopathic pulmonary fibrosis and intestinal disorders: An observational study
Idiopathic pulmonary fibrosis (IPF) is a chronic respiratory disease characterized by a progressive decline in lung function and a specific histopathologic pattern defined as usual interstitial pneumonia. Early diagnosis and new therapeutic protocols have contributed to a reduction in disease progre...
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Veröffentlicht in: | Annals of diagnostic pathology 2023-02, Vol.62, p.152072-152072, Article 152072 |
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container_title | Annals of diagnostic pathology |
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creator | Stefania, Caramaschi Angela, Bertani Stefania, Cerri Antonio, Colecchia Andrea, Ambrosini-Spaltro Gianrocco, Manco Tiziana, Salviato Luca, Reggiani Bonetti |
description | Idiopathic pulmonary fibrosis (IPF) is a chronic respiratory disease characterized by a progressive decline in lung function and a specific histopathologic pattern defined as usual interstitial pneumonia. Early diagnosis and new therapeutic protocols have contributed to a reduction in disease progression. Thus, some patients may develop extrapulmonary diseases including malignancies and chronic pathologies. The aim of this study was to investigate the frequency of intestinal disorders such as polyps, colorectal carcinoma (CRC), and chronic inflammatory bowel disease (IBD) in patients with IPF.
From the database of 189 patients with IPF (148 males, 78.3 %; 41 females, 21.7 %) residing in the district of Modena, we identified 44 patients (36 males, 81.8 %; 8 females, 18.2 %) with a histologically confirmed intestinal disease.
Intestinal polyps were detected in 41 cases (93.2 %), of which 4 were associated with CRC and 1 with IBD; 1 patient had only CRC (2.3 %), and 2 patients had only IBD (4.5 %). Both males and females developed bowel disease, but males seemed to have a higher number of polyps and high-grade adenomas with a predisposition to malignant transformation.
As patients with IPF may present with intestinal diseases that can evolve into malignancies in some cases, they should undergo appropriate follow-up and targeted colorectal screening. Thus, colorectal pathologies should not take a back seat. These preliminary results encourage further research to select suitable patients for specific diagnostic and therapeutic procedures in order to prolong survival and improve the quality of life.
•The study of Idiopathic pulmonary fibrosis (IPF) has not had many developments in recent years.•We wanted to investigate the frequency of intestinal diseases in a cohort of patients affected by IPF.•This research could open the view of this chronic respiratory disease•This research could help to identify categories of patients suitable for personalized therapy. |
doi_str_mv | 10.1016/j.anndiagpath.2022.152072 |
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From the database of 189 patients with IPF (148 males, 78.3 %; 41 females, 21.7 %) residing in the district of Modena, we identified 44 patients (36 males, 81.8 %; 8 females, 18.2 %) with a histologically confirmed intestinal disease.
Intestinal polyps were detected in 41 cases (93.2 %), of which 4 were associated with CRC and 1 with IBD; 1 patient had only CRC (2.3 %), and 2 patients had only IBD (4.5 %). Both males and females developed bowel disease, but males seemed to have a higher number of polyps and high-grade adenomas with a predisposition to malignant transformation.
As patients with IPF may present with intestinal diseases that can evolve into malignancies in some cases, they should undergo appropriate follow-up and targeted colorectal screening. Thus, colorectal pathologies should not take a back seat. These preliminary results encourage further research to select suitable patients for specific diagnostic and therapeutic procedures in order to prolong survival and improve the quality of life.
•The study of Idiopathic pulmonary fibrosis (IPF) has not had many developments in recent years.•We wanted to investigate the frequency of intestinal diseases in a cohort of patients affected by IPF.•This research could open the view of this chronic respiratory disease•This research could help to identify categories of patients suitable for personalized therapy.</description><identifier>ISSN: 1092-9134</identifier><identifier>EISSN: 1532-8198</identifier><identifier>DOI: 10.1016/j.anndiagpath.2022.152072</identifier><identifier>PMID: 36529590</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Colorectal adenocarcinoma ; Colorectal Neoplasms - complications ; Colorectal Neoplasms - diagnosis ; Colorectal Neoplasms - epidemiology ; Disease Progression ; Female ; Humans ; Idiopathic pulmonary fibrosis ; Idiopathic Pulmonary Fibrosis - diagnosis ; Idiopathic Pulmonary Fibrosis - epidemiology ; Idiopathic Pulmonary Fibrosis - pathology ; Inflammatory bowel disease ; Inflammatory Bowel Diseases - complications ; Intestinal polyps ; Male ; Quality of Life</subject><ispartof>Annals of diagnostic pathology, 2023-02, Vol.62, p.152072-152072, Article 152072</ispartof><rights>2022 Elsevier Inc.</rights><rights>Copyright © 2022 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c377t-3e66125bf8e208c1bb1f057d58427299eb4e67a5f3a3b44c4c29a425e1958acc3</citedby><cites>FETCH-LOGICAL-c377t-3e66125bf8e208c1bb1f057d58427299eb4e67a5f3a3b44c4c29a425e1958acc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.anndiagpath.2022.152072$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36529590$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stefania, Caramaschi</creatorcontrib><creatorcontrib>Angela, Bertani</creatorcontrib><creatorcontrib>Stefania, Cerri</creatorcontrib><creatorcontrib>Antonio, Colecchia</creatorcontrib><creatorcontrib>Andrea, Ambrosini-Spaltro</creatorcontrib><creatorcontrib>Gianrocco, Manco</creatorcontrib><creatorcontrib>Tiziana, Salviato</creatorcontrib><creatorcontrib>Luca, Reggiani Bonetti</creatorcontrib><title>Idiopathic pulmonary fibrosis and intestinal disorders: An observational study</title><title>Annals of diagnostic pathology</title><addtitle>Ann Diagn Pathol</addtitle><description>Idiopathic pulmonary fibrosis (IPF) is a chronic respiratory disease characterized by a progressive decline in lung function and a specific histopathologic pattern defined as usual interstitial pneumonia. Early diagnosis and new therapeutic protocols have contributed to a reduction in disease progression. Thus, some patients may develop extrapulmonary diseases including malignancies and chronic pathologies. The aim of this study was to investigate the frequency of intestinal disorders such as polyps, colorectal carcinoma (CRC), and chronic inflammatory bowel disease (IBD) in patients with IPF.
From the database of 189 patients with IPF (148 males, 78.3 %; 41 females, 21.7 %) residing in the district of Modena, we identified 44 patients (36 males, 81.8 %; 8 females, 18.2 %) with a histologically confirmed intestinal disease.
Intestinal polyps were detected in 41 cases (93.2 %), of which 4 were associated with CRC and 1 with IBD; 1 patient had only CRC (2.3 %), and 2 patients had only IBD (4.5 %). Both males and females developed bowel disease, but males seemed to have a higher number of polyps and high-grade adenomas with a predisposition to malignant transformation.
As patients with IPF may present with intestinal diseases that can evolve into malignancies in some cases, they should undergo appropriate follow-up and targeted colorectal screening. Thus, colorectal pathologies should not take a back seat. These preliminary results encourage further research to select suitable patients for specific diagnostic and therapeutic procedures in order to prolong survival and improve the quality of life.
•The study of Idiopathic pulmonary fibrosis (IPF) has not had many developments in recent years.•We wanted to investigate the frequency of intestinal diseases in a cohort of patients affected by IPF.•This research could open the view of this chronic respiratory disease•This research could help to identify categories of patients suitable for personalized therapy.</description><subject>Colorectal adenocarcinoma</subject><subject>Colorectal Neoplasms - complications</subject><subject>Colorectal Neoplasms - diagnosis</subject><subject>Colorectal Neoplasms - epidemiology</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Humans</subject><subject>Idiopathic pulmonary fibrosis</subject><subject>Idiopathic Pulmonary Fibrosis - diagnosis</subject><subject>Idiopathic Pulmonary Fibrosis - epidemiology</subject><subject>Idiopathic Pulmonary Fibrosis - pathology</subject><subject>Inflammatory bowel disease</subject><subject>Inflammatory Bowel Diseases - complications</subject><subject>Intestinal polyps</subject><subject>Male</subject><subject>Quality of Life</subject><issn>1092-9134</issn><issn>1532-8198</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkMtOwzAQRS0EgvL4BRR2bFL8jGN2VcVLqmADa8uxJ-AqtYudVOLvSdWCWLKakebembkHoSuCpwST6mY5NSE4b97Xpv-YUkzplAiKJT1AEyIYLWui6sOxx4qWijB-gk5zXmJMCBfyGJ2wSlAlFJ6g5yfn43aNt8V66FYxmPRVtL5JMftcmOAKH3rIvQ-mK5zPMTlI-baYhSI2GdLG9D5uZ7kf3Nc5OmpNl-FiX8_Q2_3d6_yxXLw8PM1ni9IyKfuSQVURKpq2BoprS5qGtFhIJ2pOJVUKGg6VNKJlhjWcW26pMpwKIErUxlp2hq53e9cpfg7je3rls4WuMwHikDWVQtQYM8lHqdpJ7RgpJ2j1OvnVmFITrLc49VL_wam3OPUO5-i93J8ZmhW4X-cPv1Ew3wlgDLvxkHS2HoIF5xPYXrvo_3HmG0uyjPM</recordid><startdate>202302</startdate><enddate>202302</enddate><creator>Stefania, Caramaschi</creator><creator>Angela, Bertani</creator><creator>Stefania, Cerri</creator><creator>Antonio, Colecchia</creator><creator>Andrea, Ambrosini-Spaltro</creator><creator>Gianrocco, Manco</creator><creator>Tiziana, Salviato</creator><creator>Luca, Reggiani Bonetti</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202302</creationdate><title>Idiopathic pulmonary fibrosis and intestinal disorders: An observational study</title><author>Stefania, Caramaschi ; Angela, Bertani ; Stefania, Cerri ; Antonio, Colecchia ; Andrea, Ambrosini-Spaltro ; Gianrocco, Manco ; Tiziana, Salviato ; Luca, Reggiani Bonetti</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c377t-3e66125bf8e208c1bb1f057d58427299eb4e67a5f3a3b44c4c29a425e1958acc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Colorectal adenocarcinoma</topic><topic>Colorectal Neoplasms - complications</topic><topic>Colorectal Neoplasms - diagnosis</topic><topic>Colorectal Neoplasms - epidemiology</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Humans</topic><topic>Idiopathic pulmonary fibrosis</topic><topic>Idiopathic Pulmonary Fibrosis - diagnosis</topic><topic>Idiopathic Pulmonary Fibrosis - epidemiology</topic><topic>Idiopathic Pulmonary Fibrosis - pathology</topic><topic>Inflammatory bowel disease</topic><topic>Inflammatory Bowel Diseases - complications</topic><topic>Intestinal polyps</topic><topic>Male</topic><topic>Quality of Life</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stefania, Caramaschi</creatorcontrib><creatorcontrib>Angela, Bertani</creatorcontrib><creatorcontrib>Stefania, Cerri</creatorcontrib><creatorcontrib>Antonio, Colecchia</creatorcontrib><creatorcontrib>Andrea, Ambrosini-Spaltro</creatorcontrib><creatorcontrib>Gianrocco, Manco</creatorcontrib><creatorcontrib>Tiziana, Salviato</creatorcontrib><creatorcontrib>Luca, Reggiani Bonetti</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of diagnostic pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stefania, Caramaschi</au><au>Angela, Bertani</au><au>Stefania, Cerri</au><au>Antonio, Colecchia</au><au>Andrea, Ambrosini-Spaltro</au><au>Gianrocco, Manco</au><au>Tiziana, Salviato</au><au>Luca, Reggiani Bonetti</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Idiopathic pulmonary fibrosis and intestinal disorders: An observational study</atitle><jtitle>Annals of diagnostic pathology</jtitle><addtitle>Ann Diagn Pathol</addtitle><date>2023-02</date><risdate>2023</risdate><volume>62</volume><spage>152072</spage><epage>152072</epage><pages>152072-152072</pages><artnum>152072</artnum><issn>1092-9134</issn><eissn>1532-8198</eissn><abstract>Idiopathic pulmonary fibrosis (IPF) is a chronic respiratory disease characterized by a progressive decline in lung function and a specific histopathologic pattern defined as usual interstitial pneumonia. Early diagnosis and new therapeutic protocols have contributed to a reduction in disease progression. Thus, some patients may develop extrapulmonary diseases including malignancies and chronic pathologies. The aim of this study was to investigate the frequency of intestinal disorders such as polyps, colorectal carcinoma (CRC), and chronic inflammatory bowel disease (IBD) in patients with IPF.
From the database of 189 patients with IPF (148 males, 78.3 %; 41 females, 21.7 %) residing in the district of Modena, we identified 44 patients (36 males, 81.8 %; 8 females, 18.2 %) with a histologically confirmed intestinal disease.
Intestinal polyps were detected in 41 cases (93.2 %), of which 4 were associated with CRC and 1 with IBD; 1 patient had only CRC (2.3 %), and 2 patients had only IBD (4.5 %). Both males and females developed bowel disease, but males seemed to have a higher number of polyps and high-grade adenomas with a predisposition to malignant transformation.
As patients with IPF may present with intestinal diseases that can evolve into malignancies in some cases, they should undergo appropriate follow-up and targeted colorectal screening. Thus, colorectal pathologies should not take a back seat. These preliminary results encourage further research to select suitable patients for specific diagnostic and therapeutic procedures in order to prolong survival and improve the quality of life.
•The study of Idiopathic pulmonary fibrosis (IPF) has not had many developments in recent years.•We wanted to investigate the frequency of intestinal diseases in a cohort of patients affected by IPF.•This research could open the view of this chronic respiratory disease•This research could help to identify categories of patients suitable for personalized therapy.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>36529590</pmid><doi>10.1016/j.anndiagpath.2022.152072</doi><tpages>1</tpages></addata></record> |
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subjects | Colorectal adenocarcinoma Colorectal Neoplasms - complications Colorectal Neoplasms - diagnosis Colorectal Neoplasms - epidemiology Disease Progression Female Humans Idiopathic pulmonary fibrosis Idiopathic Pulmonary Fibrosis - diagnosis Idiopathic Pulmonary Fibrosis - epidemiology Idiopathic Pulmonary Fibrosis - pathology Inflammatory bowel disease Inflammatory Bowel Diseases - complications Intestinal polyps Male Quality of Life |
title | Idiopathic pulmonary fibrosis and intestinal disorders: An observational study |
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