Omphalocele and biliary atresia: chance or causality. A case report

Detalhes bibliográficos
Autor(a) principal: Rosa,Julia Amim
Data de Publicação: 2022
Outros Autores: Pinto,Ana Maria Rossignolli, Del Bigio,Juliana Zoboli, Lima,Larissa Barbosa, Silva,Marcos Marques da, Mano,Rafaela Braga Cabrera, Falcão,Mário Cícero
Tipo de documento: Relatório
Idioma: eng
Título da fonte: Einstein (São Paulo)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1679-45082022000100518
Resumo: ABSTRACT To relate omphalocele and biliary atresia and investigate possible embryological correlations that justify the simultaneous occurrence. A female preterm newborn diagnosed as omphalocele; cesarean delivery, weight 2,500g, 46 XX karyotype. Initially, the newborn remained fasting and on parenteral nutrition, and enteral diet was introduced later, with good acceptance. On the 12th day of life, the newborn presented direct hyperbilirubinemia, increased levels of liver enzymes and fecal acholia, with a presumptive diagnosis of biliary atresia. However, the ultrasound was inconclusive, due to anatomical changes resulting from omphalocele. A surgical approach was chosen on the 37th day of life aiming to confirm diagnosis of biliary atresia and to repair omphalocele. During the surgical procedure, structural alterations compatible with biliary atresia were observed, later confirmed by pathological examination; a hepatoportoenterostomy was performed and the omphalocele was corrected. She evolved well in the postoperative period, with a decrease in direct bilirubin and liver enzymes, as well as resolution of fecal acholia, and was discharged in good clinical condition. This is a bizarre and extremely rare association, but the prognosis may be good when an early diagnosis is made and surgery performed, besides support and clinical management to prevent complications in the perioperative period. Although the pathogenesis of the diseases has not been fully defined yet, there is, to date, no direct relation between them. The association between omphalocele and biliary atresia is extremely uncommon, with only two published cases.
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spelling Omphalocele and biliary atresia: chance or causality. A case reportCongenital abnormalitiesBiliary atresiaHernia, umbilicalJaundiceInfant, newbornABSTRACT To relate omphalocele and biliary atresia and investigate possible embryological correlations that justify the simultaneous occurrence. A female preterm newborn diagnosed as omphalocele; cesarean delivery, weight 2,500g, 46 XX karyotype. Initially, the newborn remained fasting and on parenteral nutrition, and enteral diet was introduced later, with good acceptance. On the 12th day of life, the newborn presented direct hyperbilirubinemia, increased levels of liver enzymes and fecal acholia, with a presumptive diagnosis of biliary atresia. However, the ultrasound was inconclusive, due to anatomical changes resulting from omphalocele. A surgical approach was chosen on the 37th day of life aiming to confirm diagnosis of biliary atresia and to repair omphalocele. During the surgical procedure, structural alterations compatible with biliary atresia were observed, later confirmed by pathological examination; a hepatoportoenterostomy was performed and the omphalocele was corrected. She evolved well in the postoperative period, with a decrease in direct bilirubin and liver enzymes, as well as resolution of fecal acholia, and was discharged in good clinical condition. This is a bizarre and extremely rare association, but the prognosis may be good when an early diagnosis is made and surgery performed, besides support and clinical management to prevent complications in the perioperative period. Although the pathogenesis of the diseases has not been fully defined yet, there is, to date, no direct relation between them. The association between omphalocele and biliary atresia is extremely uncommon, with only two published cases.Instituto Israelita de Ensino e Pesquisa Albert Einstein2022-01-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1679-45082022000100518einstein (São Paulo) v.20 2022reponame:Einstein (São Paulo)instname:Instituto Israelita de Ensino e Pesquisa Albert Einstein (IIEPAE)instacron:IIEPAE10.31744/einstein_journal/2022rc0072info:eu-repo/semantics/openAccessRosa,Julia AmimPinto,Ana Maria RossignolliDel Bigio,Juliana ZoboliLima,Larissa BarbosaSilva,Marcos Marques daMano,Rafaela Braga CabreraFalcão,Mário Cíceroeng2022-09-20T00:00:00Zoai:scielo:S1679-45082022000100518Revistahttps://journal.einstein.br/pt-br/ONGhttps://old.scielo.br/oai/scielo-oai.php||revista@einstein.br2317-63851679-4508opendoar:2022-09-20T00:00Einstein (São Paulo) - Instituto Israelita de Ensino e Pesquisa Albert Einstein (IIEPAE)false
dc.title.none.fl_str_mv Omphalocele and biliary atresia: chance or causality. A case report
title Omphalocele and biliary atresia: chance or causality. A case report
spellingShingle Omphalocele and biliary atresia: chance or causality. A case report
Rosa,Julia Amim
Congenital abnormalities
Biliary atresia
Hernia, umbilical
Jaundice
Infant, newborn
title_short Omphalocele and biliary atresia: chance or causality. A case report
title_full Omphalocele and biliary atresia: chance or causality. A case report
title_fullStr Omphalocele and biliary atresia: chance or causality. A case report
title_full_unstemmed Omphalocele and biliary atresia: chance or causality. A case report
title_sort Omphalocele and biliary atresia: chance or causality. A case report
author Rosa,Julia Amim
author_facet Rosa,Julia Amim
Pinto,Ana Maria Rossignolli
Del Bigio,Juliana Zoboli
Lima,Larissa Barbosa
Silva,Marcos Marques da
Mano,Rafaela Braga Cabrera
Falcão,Mário Cícero
author_role author
author2 Pinto,Ana Maria Rossignolli
Del Bigio,Juliana Zoboli
Lima,Larissa Barbosa
Silva,Marcos Marques da
Mano,Rafaela Braga Cabrera
Falcão,Mário Cícero
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Rosa,Julia Amim
Pinto,Ana Maria Rossignolli
Del Bigio,Juliana Zoboli
Lima,Larissa Barbosa
Silva,Marcos Marques da
Mano,Rafaela Braga Cabrera
Falcão,Mário Cícero
dc.subject.por.fl_str_mv Congenital abnormalities
Biliary atresia
Hernia, umbilical
Jaundice
Infant, newborn
topic Congenital abnormalities
Biliary atresia
Hernia, umbilical
Jaundice
Infant, newborn
description ABSTRACT To relate omphalocele and biliary atresia and investigate possible embryological correlations that justify the simultaneous occurrence. A female preterm newborn diagnosed as omphalocele; cesarean delivery, weight 2,500g, 46 XX karyotype. Initially, the newborn remained fasting and on parenteral nutrition, and enteral diet was introduced later, with good acceptance. On the 12th day of life, the newborn presented direct hyperbilirubinemia, increased levels of liver enzymes and fecal acholia, with a presumptive diagnosis of biliary atresia. However, the ultrasound was inconclusive, due to anatomical changes resulting from omphalocele. A surgical approach was chosen on the 37th day of life aiming to confirm diagnosis of biliary atresia and to repair omphalocele. During the surgical procedure, structural alterations compatible with biliary atresia were observed, later confirmed by pathological examination; a hepatoportoenterostomy was performed and the omphalocele was corrected. She evolved well in the postoperative period, with a decrease in direct bilirubin and liver enzymes, as well as resolution of fecal acholia, and was discharged in good clinical condition. This is a bizarre and extremely rare association, but the prognosis may be good when an early diagnosis is made and surgery performed, besides support and clinical management to prevent complications in the perioperative period. Although the pathogenesis of the diseases has not been fully defined yet, there is, to date, no direct relation between them. The association between omphalocele and biliary atresia is extremely uncommon, with only two published cases.
publishDate 2022
dc.date.none.fl_str_mv 2022-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/report
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dc.language.iso.fl_str_mv eng
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dc.relation.none.fl_str_mv 10.31744/einstein_journal/2022rc0072
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dc.publisher.none.fl_str_mv Instituto Israelita de Ensino e Pesquisa Albert Einstein
publisher.none.fl_str_mv Instituto Israelita de Ensino e Pesquisa Albert Einstein
dc.source.none.fl_str_mv einstein (São Paulo) v.20 2022
reponame:Einstein (São Paulo)
instname:Instituto Israelita de Ensino e Pesquisa Albert Einstein (IIEPAE)
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instname_str Instituto Israelita de Ensino e Pesquisa Albert Einstein (IIEPAE)
instacron_str IIEPAE
institution IIEPAE
reponame_str Einstein (São Paulo)
collection Einstein (São Paulo)
repository.name.fl_str_mv Einstein (São Paulo) - Instituto Israelita de Ensino e Pesquisa Albert Einstein (IIEPAE)
repository.mail.fl_str_mv ||revista@einstein.br
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