Hepatoportoenterostomy surgery technique
Biliary atresia (BA) is a pathology that causes jaundice in children because of an obstruction of the obliterated biliary tract. Despite being considered a rare disease, the incidence can reach 1/2400 live births in the Pacific region. The etiology is unknown. If untreated, it will lead to cirrhosis...
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| Veröffentlicht in: | Journal of pediatric surgery 2019-08, Vol.54 (8), p.1715-1718 |
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| container_issue | 8 |
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| container_title | Journal of pediatric surgery |
| container_volume | 54 |
| creator | de Carvalho, Nubyhélia Maria Negreiro Torres, Sarah Monte Cavalcante, Joyce Carolle Bezerra Ximenes, Ana Clemilda Marques Junior, Jose Albuquerque Landim da Silveira Moreira, Sérgio Oceliano |
| description | Biliary atresia (BA) is a pathology that causes jaundice in children because of an obstruction of the obliterated biliary tract. Despite being considered a rare disease, the incidence can reach 1/2400 live births in the Pacific region. The etiology is unknown. If untreated, it will lead to cirrhosis and death. Early operation (within 60 days after birth) is the most important prognostic factor. The objective of this article is to present the technical description step by step of a hepatoportoenterostomy operation in a female 61 days of age with BA. |
| doi_str_mv | 10.1016/j.jpedsurg.2018.10.041 |
| format | Article |
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Despite being considered a rare disease, the incidence can reach 1/2400 live births in the Pacific region. The etiology is unknown. If untreated, it will lead to cirrhosis and death. Early operation (within 60 days after birth) is the most important prognostic factor. The objective of this article is to present the technical description step by step of a hepatoportoenterostomy operation in a female 61 days of age with BA.</description><identifier>ISSN: 0022-3468</identifier><identifier>EISSN: 1531-5037</identifier><identifier>DOI: 10.1016/j.jpedsurg.2018.10.041</identifier><identifier>PMID: 30442462</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Biliary atresia ; Biliary Atresia - complications ; Biliary Atresia - surgery ; Female ; Hepatoportoenterostomy ; Humans ; Infant ; Jaundice ; Jaundice - etiology ; Portoenterostomy, Hepatic - methods</subject><ispartof>Journal of pediatric surgery, 2019-08, Vol.54 (8), p.1715-1718</ispartof><rights>2018 Elsevier Inc.</rights><rights>Copyright © 2018 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-9b63f33c885da4033c267a698cbf2f01b73c1d2aa651e5f9467c74c80fe1e4e83</citedby><cites>FETCH-LOGICAL-c368t-9b63f33c885da4033c267a698cbf2f01b73c1d2aa651e5f9467c74c80fe1e4e83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jpedsurg.2018.10.041$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30442462$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>de Carvalho, Nubyhélia Maria Negreiro</creatorcontrib><creatorcontrib>Torres, Sarah Monte</creatorcontrib><creatorcontrib>Cavalcante, Joyce Carolle Bezerra</creatorcontrib><creatorcontrib>Ximenes, Ana Clemilda Marques</creatorcontrib><creatorcontrib>Junior, Jose Albuquerque Landim</creatorcontrib><creatorcontrib>da Silveira Moreira, Sérgio Oceliano</creatorcontrib><title>Hepatoportoenterostomy surgery technique</title><title>Journal of pediatric surgery</title><addtitle>J Pediatr Surg</addtitle><description>Biliary atresia (BA) is a pathology that causes jaundice in children because of an obstruction of the obliterated biliary tract. Despite being considered a rare disease, the incidence can reach 1/2400 live births in the Pacific region. The etiology is unknown. If untreated, it will lead to cirrhosis and death. Early operation (within 60 days after birth) is the most important prognostic factor. The objective of this article is to present the technical description step by step of a hepatoportoenterostomy operation in a female 61 days of age with BA.</description><subject>Biliary atresia</subject><subject>Biliary Atresia - complications</subject><subject>Biliary Atresia - surgery</subject><subject>Female</subject><subject>Hepatoportoenterostomy</subject><subject>Humans</subject><subject>Infant</subject><subject>Jaundice</subject><subject>Jaundice - etiology</subject><subject>Portoenterostomy, Hepatic - methods</subject><issn>0022-3468</issn><issn>1531-5037</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEFPwzAMhSMEYmPwF6Ydd2mJkzTtbqAJGNIkLnCO0tSFVltTkhRp_55U27hysvX07Gd_hMyBpkBB3rdp22PlB_eZMgpFFFMq4IJMIeOQZJTnl2RKKWMJF7KYkBvvW0qjTOGaTDgVggnJpmS5wV4H21sXLHYBnfXB7g-LcTO6wyKg-eqa7wFvyVWtdx7vTnVGPp6f3tebZPv28rp-3CaGyyIkq1LymnNTFFmlBY0dk7mWq8KUNasplDk3UDGtZQaY1Sshc5MLU9AaAQUWfEaWx729szHWB7VvvMHdTndoB68Y8Aw4sPjnjMij1cSrvcNa9a7Za3dQQNVISbXqTEmNlEY9UoqD81PGUO6x-hs7Y4mGh6MB46c_DTrlTYOdwapxaIKqbPNfxi-nenwI</recordid><startdate>201908</startdate><enddate>201908</enddate><creator>de Carvalho, Nubyhélia Maria Negreiro</creator><creator>Torres, Sarah Monte</creator><creator>Cavalcante, Joyce Carolle Bezerra</creator><creator>Ximenes, Ana Clemilda Marques</creator><creator>Junior, Jose Albuquerque Landim</creator><creator>da Silveira Moreira, Sérgio Oceliano</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>201908</creationdate><title>Hepatoportoenterostomy surgery technique</title><author>de Carvalho, Nubyhélia Maria Negreiro ; Torres, Sarah Monte ; Cavalcante, Joyce Carolle Bezerra ; Ximenes, Ana Clemilda Marques ; Junior, Jose Albuquerque Landim ; da Silveira Moreira, Sérgio Oceliano</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-9b63f33c885da4033c267a698cbf2f01b73c1d2aa651e5f9467c74c80fe1e4e83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Biliary atresia</topic><topic>Biliary Atresia - complications</topic><topic>Biliary Atresia - surgery</topic><topic>Female</topic><topic>Hepatoportoenterostomy</topic><topic>Humans</topic><topic>Infant</topic><topic>Jaundice</topic><topic>Jaundice - etiology</topic><topic>Portoenterostomy, Hepatic - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Carvalho, Nubyhélia Maria Negreiro</creatorcontrib><creatorcontrib>Torres, Sarah Monte</creatorcontrib><creatorcontrib>Cavalcante, Joyce Carolle Bezerra</creatorcontrib><creatorcontrib>Ximenes, Ana Clemilda Marques</creatorcontrib><creatorcontrib>Junior, Jose Albuquerque Landim</creatorcontrib><creatorcontrib>da Silveira Moreira, Sérgio Oceliano</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>Journal of pediatric surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Carvalho, Nubyhélia Maria Negreiro</au><au>Torres, Sarah Monte</au><au>Cavalcante, Joyce Carolle Bezerra</au><au>Ximenes, Ana Clemilda Marques</au><au>Junior, Jose Albuquerque Landim</au><au>da Silveira Moreira, Sérgio Oceliano</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hepatoportoenterostomy surgery technique</atitle><jtitle>Journal of pediatric surgery</jtitle><addtitle>J Pediatr Surg</addtitle><date>2019-08</date><risdate>2019</risdate><volume>54</volume><issue>8</issue><spage>1715</spage><epage>1718</epage><pages>1715-1718</pages><issn>0022-3468</issn><eissn>1531-5037</eissn><abstract>Biliary atresia (BA) is a pathology that causes jaundice in children because of an obstruction of the obliterated biliary tract. Despite being considered a rare disease, the incidence can reach 1/2400 live births in the Pacific region. The etiology is unknown. If untreated, it will lead to cirrhosis and death. Early operation (within 60 days after birth) is the most important prognostic factor. The objective of this article is to present the technical description step by step of a hepatoportoenterostomy operation in a female 61 days of age with BA.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>30442462</pmid><doi>10.1016/j.jpedsurg.2018.10.041</doi><tpages>4</tpages></addata></record> |
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| ispartof | Journal of pediatric surgery, 2019-08, Vol.54 (8), p.1715-1718 |
| issn | 0022-3468 1531-5037 |
| language | eng |
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| source | MEDLINE; Access via ScienceDirect (Elsevier) |
| subjects | Biliary atresia Biliary Atresia - complications Biliary Atresia - surgery Female Hepatoportoenterostomy Humans Infant Jaundice Jaundice - etiology Portoenterostomy, Hepatic - methods |
| title | Hepatoportoenterostomy surgery technique |
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