Literature DB >> 26577909

A pathological scoring system in the diagnosis and judgment of prognosis of biliary atresia.

Gong Chen1, Ping Xue1, Shan Zheng2, Lian Chen3, Yangyang Ma3.   

Abstract

OBJECTIVE: The purpose of this study was to evaluate the diagnostic and prognostic value of a histological scoring system in biliary atresia (BA).
METHODS: From June 2013 to July 2014, 86 wedge liver biopsy specimens were obtained from infants with neonatal cholestasis (58 patients with biliary atresia and 28 patients with non-obstructive cholestasis as control) in our center. A pathologist, single-blinded to the final diagnosis, made the histological diagnosis individually based on an 8-feature (liver fibrosis, portal ductal proliferation, bile plugs in portal ductules, cholestasis, hepatocellular changes inflammatory cells infiltration in portal region, extramedullary hematopoiesis, and ductal plate malformation), 21-point (0 to 21) scoring system.
RESULTS: In this retrospective study, ductular reaction (bile ductular proliferation) and liver fibrosis in the portal area, bile plugs, and ductal plate malformation were the best indicators of BA. With the scoring system, a score of ≥8 had the best diagnostic utility to differentiate BA from other intrahepatic cholestasis histologically (sensitivity 94.7%, specificity 86.2%, accuracy 91.9%). Liver fibrosis and ductal plate malformation were confirmed to be related with the prognosis.
CONCLUSIONS: An 8-feature, 21-point histological scoring system has a good diagnostic accuracy in the interpretation of liver histology in neonatal cholestasis. The use of liver fibrosis and ductal plate malformation are also feasible to assess the prognosis.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Biliary atresia; Diagnosis; Liver histopathology; Prognosis; Scoring system

Mesh:

Year:  2015        PMID: 26577909     DOI: 10.1016/j.jpedsurg.2015.08.041

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


  11 in total

1.  Clinical and pathological features of patients with biliary atresia who survived for more than 5 years with native liver.

Authors:  Song Sun; Shan Zheng; Xuexin Lu; Gong Chen; Yangyang Ma; Lian Chen; Kuiran Dong
Journal:  Pediatr Surg Int       Date:  2018-02-09       Impact factor: 1.827

2.  Prognostic factors indicating survival with native liver after Kasai procedure for biliary atresia.

Authors:  Juma Obayashi; Kohei Kawaguchi; Shutaro Manabe; Hideki Nagae; Munechika Wakisaka; Junki Koike; Masayuki Takagi; Hiroaki Kitagawa
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7.  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

8.  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

Review 9.  Biliary Atresia Animal Models: Is the Needle in a Haystack?

Authors:  Nutan Pal; Parijat S Joy; Consolato M Sergi
Journal:  Int J Mol Sci       Date:  2022-07-16       Impact factor: 6.208

10.  Development and validation of bile acid profile-based scoring system for identification of biliary atresia: a prospective study.

Authors:  Dongying Zhao; Kejun Zhou; Yan Chen; Wei Xie; Yongjun Zhang
Journal:  BMC Pediatr       Date:  2020-05-27       Impact factor: 2.125

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