Gastrointestinal malignancy in cystic fibrosis
Cystic fibrosis (CF) is a multisystem disease affecting the gastrointestinal (GI) tract as well as the lungs. As survival has increased significantly over the past few decades, complications not seen previously have become apparent. There is an overall increased rate of malignancy in CF, particularl...
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Veröffentlicht in: | Paediatric respiratory reviews 2020-09, Vol.35, p.90-92 |
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creator | Hough, Natasha Emily Chapman, Stephen James Flight, William George |
description | Cystic fibrosis (CF) is a multisystem disease affecting the gastrointestinal (GI) tract as well as the lungs. As survival has increased significantly over the past few decades, complications not seen previously have become apparent. There is an overall increased rate of malignancy in CF, particularly from the GI tract and in the post-transplant population. The most common sites of malignancy are the pancreatico-biliary and digestive tract, as well as an increased rate of testicular cancer. Using an illustrative case of metastatic oesophageal malignancy which initially appeared to be hepatic in origin, we have reviewed the literature surrounding malignancy in CF with a particular focus on the GI tract. |
doi_str_mv | 10.1016/j.prrv.2020.03.002 |
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As survival has increased significantly over the past few decades, complications not seen previously have become apparent. There is an overall increased rate of malignancy in CF, particularly from the GI tract and in the post-transplant population. The most common sites of malignancy are the pancreatico-biliary and digestive tract, as well as an increased rate of testicular cancer. 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As survival has increased significantly over the past few decades, complications not seen previously have become apparent. There is an overall increased rate of malignancy in CF, particularly from the GI tract and in the post-transplant population. The most common sites of malignancy are the pancreatico-biliary and digestive tract, as well as an increased rate of testicular cancer. Using an illustrative case of metastatic oesophageal malignancy which initially appeared to be hepatic in origin, we have reviewed the literature surrounding malignancy in CF with a particular focus on the GI tract.</description><subject>Cancer screening</subject><subject>Colon cancer</subject><subject>Cystic fibrosis</subject><subject>Metastases</subject><subject>Oesophageal cancer</subject><issn>1526-0542</issn><issn>1526-0550</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kE9LAzEQxYMoWKtfwNMevew6M9lkt-BFiv-g4EXPIZtNJGWbrcm20G9vSsWjpxmG94b3fozdIlQIKO_X1TbGfUVAUAGvAOiMzVCQLEEIOP_ba7pkVymtARAl4IxVLzpNcfRhsmnyQQ_FRg_-K-hgDoUPhTnksymc7-KYfLpmF04Pyd78zjn7fH76WL6Wq_eXt-XjqjSc86kUwJFaWjRd3yzaVmMvwNjO8Y6c4E73rSTNu5pT3baid41sUOuFFB0ngMbxObs7_d3G8XuXo6mNT8YOgw523CVFNUKDtcQ6S-kkNTlhitapbfQbHQ8KQR3hqLU6wlFHOAq4ynCy6eFksrnE3tuokvE2GNv7aM2k-tH_Z_8ByeNsrQ</recordid><startdate>202009</startdate><enddate>202009</enddate><creator>Hough, Natasha Emily</creator><creator>Chapman, Stephen James</creator><creator>Flight, William George</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202009</creationdate><title>Gastrointestinal malignancy in cystic fibrosis</title><author>Hough, Natasha Emily ; Chapman, Stephen James ; Flight, William George</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c333t-503128297bd7988a1d50cebf3b2f53fad862a3b4324885df7671aa965b32007f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Cancer screening</topic><topic>Colon cancer</topic><topic>Cystic fibrosis</topic><topic>Metastases</topic><topic>Oesophageal cancer</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hough, Natasha Emily</creatorcontrib><creatorcontrib>Chapman, Stephen James</creatorcontrib><creatorcontrib>Flight, William George</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Paediatric respiratory reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hough, Natasha Emily</au><au>Chapman, Stephen James</au><au>Flight, William George</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gastrointestinal malignancy in cystic fibrosis</atitle><jtitle>Paediatric respiratory reviews</jtitle><date>2020-09</date><risdate>2020</risdate><volume>35</volume><spage>90</spage><epage>92</epage><pages>90-92</pages><issn>1526-0542</issn><eissn>1526-0550</eissn><abstract>Cystic fibrosis (CF) is a multisystem disease affecting the gastrointestinal (GI) tract as well as the lungs. As survival has increased significantly over the past few decades, complications not seen previously have become apparent. There is an overall increased rate of malignancy in CF, particularly from the GI tract and in the post-transplant population. The most common sites of malignancy are the pancreatico-biliary and digestive tract, as well as an increased rate of testicular cancer. Using an illustrative case of metastatic oesophageal malignancy which initially appeared to be hepatic in origin, we have reviewed the literature surrounding malignancy in CF with a particular focus on the GI tract.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.prrv.2020.03.002</doi><tpages>3</tpages></addata></record> |
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subjects | Cancer screening Colon cancer Cystic fibrosis Metastases Oesophageal cancer |
title | Gastrointestinal malignancy in cystic fibrosis |
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