Literature DB >> 30442462

Hepatoportoenterostomy surgery technique.

Nubyhélia Maria Negreiro de Carvalho1, Sarah Monte Torres2, Joyce Carolle Bezerra Cavalcante2, Ana Clemilda Marques Ximenes2, Jose Albuquerque Landim Junior3, Sérgio Oceliano da Silveira Moreira4.   

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.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Biliary atresia; Hepatoportoenterostomy; Jaundice

Mesh:

Year:  2018        PMID: 30442462     DOI: 10.1016/j.jpedsurg.2018.10.041

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  6 in total

Review 1.  Biliary Atresia: A Complex Hepatobiliary Disease with Variable Gene Involvement, Diagnostic Procedures, and Prognosis.

Authors:  Consolato M Sergi; Susan Gilmour
Journal:  Diagnostics (Basel)       Date:  2022-01-27

2.  Combination of gamma-glutamyl transferase and liver stiffness measurement for biliary atresia screening at different ages: a retrospective analysis of 282 infants.

Authors:  Qiulong Shen; Sarah Siyin Tan; Zengmeng Wang; Siyu Cai; Wenbo Pang; Chunhui Peng; Yajun Chen
Journal:  BMC Pediatr       Date:  2020-06-04       Impact factor: 2.125

3.  Liver stiffness measurement predicts the difficulty of Kasai procedure in biliary atresia: a single center retrospective analysis of 199 patients.

Authors:  Qiulong Shen; Yajun Chen; Chunhui Peng; Wenbo Pang; Zengmeng Wang; Dongyang Wu; Kai Wang; Xinjie Huang
Journal:  BMC Pediatr       Date:  2019-11-29       Impact factor: 2.125

4.  Short- and long-term outcomes after Kasai operation for type III biliary atresia: Twenty years of experience in a single tertiary Egyptian center-A retrospective cohort study.

Authors:  Emad Hamdy Gad; Yasmin Kamel; Tahany Abdel-Hameed Salem; Mohammed Abdel-Hafez Ali; Ahmed Nabil Sallam
Journal:  Ann Med Surg (Lond)       Date:  2021-01-23

5.  Whole exome sequencing analysis for mutations in isolated type III biliary atresia patients.

Authors:  Kubilay Gürünlüoğlu; Ahmet Koç; Kübra Durmuş; Harika Gözükara Bağ; Canan Ceran; Semra Gürünlüoğlu; Turan Yıldız; Mehmet Gül; Mehmet Demircan
Journal:  Clin Exp Hepatol       Date:  2020-12-30

6.  Case Report: Kasai Operation in Biliary Atresia After Extensive Bowel Resection.

Authors:  Szu-Han Chen; Kai-Chi Chang; Jia-Feng Wu; Huey-Ling Chen; Wen-Hsi Lin
Journal:  Front Surg       Date:  2022-01-24
  6 in total

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