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A novel approach for repair of right sided congenital diaphragmatic hernia and hepatopulmonary fusion
Abstract Right sided congenital diaphragmatic hernia (CDH) associated with hepatopulmonary fusion (HPF) is a rare congenital anomaly in which the herniated liver is fused with lung parenchyma. We discuss the case of an infant with right-sided CDH and HPF found on index operation for repair of right-...
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Published in: | Journal of surgical case reports 2024-09, Vol.2024 (9), p.rjae566 |
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creator | Cain-Trivette, Caitlin J Robinson, Newell Bryce Kadenhe-Chiweshe, Angela Steigman, Shaun Spigland, Nitsana A |
description | Abstract
Right sided congenital diaphragmatic hernia (CDH) associated with hepatopulmonary fusion (HPF) is a rare congenital anomaly in which the herniated liver is fused with lung parenchyma. We discuss the case of an infant with right-sided CDH and HPF found on index operation for repair of right-sided CDH. Due to the high incidence of vascular anomalies associated with HPF the decision was made to close the patient and get further imaging to characterize the HPF before returning to the operating room for definitive repair. We describe a novel and successful operative approach where the liver was left entirely fused to the lung and the liver was partially brought down from the chest and was plicated to the diaphragm form a seal between the parietal and pleural cavities to repair the CDH. |
doi_str_mv | 10.1093/jscr/rjae566 |
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Right sided congenital diaphragmatic hernia (CDH) associated with hepatopulmonary fusion (HPF) is a rare congenital anomaly in which the herniated liver is fused with lung parenchyma. We discuss the case of an infant with right-sided CDH and HPF found on index operation for repair of right-sided CDH. Due to the high incidence of vascular anomalies associated with HPF the decision was made to close the patient and get further imaging to characterize the HPF before returning to the operating room for definitive repair. We describe a novel and successful operative approach where the liver was left entirely fused to the lung and the liver was partially brought down from the chest and was plicated to the diaphragm form a seal between the parietal and pleural cavities to repair the CDH.</description><identifier>ISSN: 2042-8812</identifier><identifier>EISSN: 2042-8812</identifier><identifier>DOI: 10.1093/jscr/rjae566</identifier><identifier>PMID: 39239144</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Case Report</subject><ispartof>Journal of surgical case reports, 2024-09, Vol.2024 (9), p.rjae566</ispartof><rights>Published by Oxford University Press and JSCR Publishing Ltd. © The Author(s) 2024. 2024</rights><rights>Published by Oxford University Press and JSCR Publishing Ltd. © The Author(s) 2024.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c304t-5fa1d1b9f2813b422af8d759f0f6998fd8eabe793a60fa7bd0faf2e8be2e3cc93</cites><orcidid>0000-0003-4141-275X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11374373/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11374373/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,1604,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39239144$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cain-Trivette, Caitlin J</creatorcontrib><creatorcontrib>Robinson, Newell Bryce</creatorcontrib><creatorcontrib>Kadenhe-Chiweshe, Angela</creatorcontrib><creatorcontrib>Steigman, Shaun</creatorcontrib><creatorcontrib>Spigland, Nitsana A</creatorcontrib><title>A novel approach for repair of right sided congenital diaphragmatic hernia and hepatopulmonary fusion</title><title>Journal of surgical case reports</title><addtitle>J Surg Case Rep</addtitle><description>Abstract
Right sided congenital diaphragmatic hernia (CDH) associated with hepatopulmonary fusion (HPF) is a rare congenital anomaly in which the herniated liver is fused with lung parenchyma. We discuss the case of an infant with right-sided CDH and HPF found on index operation for repair of right-sided CDH. Due to the high incidence of vascular anomalies associated with HPF the decision was made to close the patient and get further imaging to characterize the HPF before returning to the operating room for definitive repair. We describe a novel and successful operative approach where the liver was left entirely fused to the lung and the liver was partially brought down from the chest and was plicated to the diaphragm form a seal between the parietal and pleural cavities to repair the CDH.</description><subject>Case Report</subject><issn>2042-8812</issn><issn>2042-8812</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><recordid>eNp9kc1r3DAQxUVJaUKaW85Ft_SQTfThta1TCCFfEOilOYuxNFprsSVVsgP97-uwm5BeMoeZB_PjzcAj5JSzC86UvNwWky_zFnBd11_IkWCVWLUtFwcf9CE5KWXLlqoU5239jRxKJaTiVXVE8JqG-IIDhZRyBNNTFzPNmMBnGh3NftNPtHiLlpoYNhj8BAO1HlKfYTPC5A3tMQcPFIJdZIIppnkYY4D8l7q5-Bi-k68OhoIn-3lMnu9uf988rJ5-3T_eXD-tjGTVtFo74JZ3yomWy64SAlxrm7VyzNVKtc62CB02SkLNHDSdXboT2HYoUBqj5DG52vmmuRvRGgxThkGn7MflGR3B6_83wfd6E18057KpZCMXh597hxz_zFgmPfpicBggYJyLlpxxIZls6gU936Emx1Iyuvc7nOnXdPRrOnqfzoL_-PjbO_yWxQKc7YA4p8-t_gFWYZ3p</recordid><startdate>20240905</startdate><enddate>20240905</enddate><creator>Cain-Trivette, Caitlin J</creator><creator>Robinson, Newell Bryce</creator><creator>Kadenhe-Chiweshe, Angela</creator><creator>Steigman, Shaun</creator><creator>Spigland, Nitsana A</creator><general>Oxford University Press</general><scope>TOX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-4141-275X</orcidid></search><sort><creationdate>20240905</creationdate><title>A novel approach for repair of right sided congenital diaphragmatic hernia and hepatopulmonary fusion</title><author>Cain-Trivette, Caitlin J ; Robinson, Newell Bryce ; Kadenhe-Chiweshe, Angela ; Steigman, Shaun ; Spigland, Nitsana A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c304t-5fa1d1b9f2813b422af8d759f0f6998fd8eabe793a60fa7bd0faf2e8be2e3cc93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Case Report</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cain-Trivette, Caitlin J</creatorcontrib><creatorcontrib>Robinson, Newell Bryce</creatorcontrib><creatorcontrib>Kadenhe-Chiweshe, Angela</creatorcontrib><creatorcontrib>Steigman, Shaun</creatorcontrib><creatorcontrib>Spigland, Nitsana A</creatorcontrib><collection>Oxford Journals Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of surgical case reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cain-Trivette, Caitlin J</au><au>Robinson, Newell Bryce</au><au>Kadenhe-Chiweshe, Angela</au><au>Steigman, Shaun</au><au>Spigland, Nitsana A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A novel approach for repair of right sided congenital diaphragmatic hernia and hepatopulmonary fusion</atitle><jtitle>Journal of surgical case reports</jtitle><addtitle>J Surg Case Rep</addtitle><date>2024-09-05</date><risdate>2024</risdate><volume>2024</volume><issue>9</issue><spage>rjae566</spage><pages>rjae566-</pages><issn>2042-8812</issn><eissn>2042-8812</eissn><abstract>Abstract
Right sided congenital diaphragmatic hernia (CDH) associated with hepatopulmonary fusion (HPF) is a rare congenital anomaly in which the herniated liver is fused with lung parenchyma. We discuss the case of an infant with right-sided CDH and HPF found on index operation for repair of right-sided CDH. Due to the high incidence of vascular anomalies associated with HPF the decision was made to close the patient and get further imaging to characterize the HPF before returning to the operating room for definitive repair. We describe a novel and successful operative approach where the liver was left entirely fused to the lung and the liver was partially brought down from the chest and was plicated to the diaphragm form a seal between the parietal and pleural cavities to repair the CDH.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>39239144</pmid><doi>10.1093/jscr/rjae566</doi><orcidid>https://orcid.org/0000-0003-4141-275X</orcidid><oa>free_for_read</oa></addata></record> |
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source | Oxford Journals Open Access; Open Access: PubMed Central |
subjects | Case Report |
title | A novel approach for repair of right sided congenital diaphragmatic hernia and hepatopulmonary fusion |
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