Literature DB >> 27504296

Diagnostic and Prognostic Significance of Various Histopathological Features in Extrahepatic Biliary Atresia.

Shenbagam Jeevakarunyam Muthukanagarajan1, Indumathi Karnan2, Padmanaban Srinivasan3, Pappathi Sadagopan4, Saraswathy Manickam5.   

Abstract

INTRODUCTION: Extrahepatic biliary atresia is a progressive disorder characterised by fibroinflammatory obliteration or stenosis of the extrahepatic biliary tree leading to obstruction of bile flow and cholestatic jaundice. It is the most common cause for cholestasis in newborn. Histopathological criteria for diagnosing biliary atresia from liver biopsy have not been clearly defined. AIM: This study was undertaken to analyse the significance of the various histopathological features in diagnosis and prognosis of extrahepatic biliary atresia from liver biopsy specimens.
MATERIALS AND METHODS: This was a retrospective study of 43 cases of extra-hepatic biliary atresia diagnosed and treated at a tertiary care hospital between January 2010 to December 2014. Formalin fixed paraffin embedded liver biopsy tissues were processed by standard technique and the slides were stained with haematoxylin and eosin. All the slides were reviewed and graded by a semi-quantitative scoring system. Features such as increased age at kasai's portoenterostomy, portal fibrosis, bile duct proliferation, cholestasis, portal inflammation and duct plate malformation were studied. Statistical analysis was worked out using SPSS 17.0 (statistical package for the social science software). Chi-square test was used to find association between various parameters with respect to mortality and Kaplan-Meier estimator was used for survival analysis of the population under study.
RESULTS: In this study comprising of 43 cases, only 6 cases (13.95%) were alive at the end of 6 months follow-up. Twenty patients who died and the 17 cases with poor survival had greater degrees of fibrosis, bile duct proliferation and cholestasis. Majority of the cases with duct plate malformation expired inspite of earlier surgical intervention. Thus proving the association of fibrosis, bile duct proliferation, cholestasis and duct plate malformation with the survival and prognosis of biliary atresia cases. Age at surgery did not show any correlation with prognosis as cases operated even at <60 days had poor survival.
CONCLUSION: From this study it can be concluded that in extrahepatic biliary atresia patients, presence of duct plate malformation, greater degrees of fibrosis, bile duct proliferation and cholestasis were strongly associated with poor prognosis.

Entities:  

Keywords:  Bile duct proliferation; Duct plate malformation; Extra-hepatic biliary atresia; Portal fibrosis; Portal inflammation

Year:  2016        PMID: 27504296      PMCID: PMC4963656          DOI: 10.7860/JCDR/2016/19252.8035

Source DB:  PubMed          Journal:  J Clin Diagn Res        ISSN: 0973-709X


  31 in total

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  8 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.  The combination of conventional ultrasound and shear-wave elastography in evaluating the segmental heterogeneity of liver fibrosis in biliary atresia patients after Kasai portoenterostomy.

Authors:  Wenying Zhou; Xiaoju Li; Nan Zhang; Bing Liao; Xiaoyan Xie; Xiaoer Zhang; Guotao Wang; Luyao Zhou
Journal:  Pediatr Surg Int       Date:  2021-05-09       Impact factor: 1.827

3.  False-negative Hepatobiliary Scintigraphy for Biliary Atresia.

Authors:  Hyunji Kim; Sujin Park; Sejin Ha; Jae Seung Kim; Dae Yeon Kim; Minyoung Oh
Journal:  Nucl Med Mol Imaging       Date:  2019-08-21

Review 4.  Early and Peri-operative Prognostic Indicators in Infants Undergoing Hepatic Portoenterostomy for Biliary Atresia: a Review.

Authors:  Robert N Lopez; Chee Y Ooi; Usha Krishnan
Journal:  Curr Gastroenterol Rep       Date:  2017-04

5.  Histopathological findings for prediction of liver cirrhosis and survival in biliary atresia patients after Kasai procedure.

Authors:  Dian Nirmala Sirait; Leila Rakhma Budiarti; Vincentia Meta Widya Paramita; Aditya Rifqi Fauzi; Fiko Ryantono; Dwiki Afandy; Naomi Yoshuantari; Hanggoro Tri Rinonce; Akhmad Makhmudi
Journal:  Diagn Pathol       Date:  2020-07-02       Impact factor: 2.644

6.  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

7.  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

8.  Growth Factors Assessed during Kasai Procedure in Liver and Serum Are Not Predictive for the Postoperative Liver Deterioration in Infants with Biliary Atresia.

Authors:  Omid Madadi-Sanjani; Stephanie Froemmel; Christine S Falk; Gertrud Vieten; Claus Petersen; Joachim F Kuebler; Christian Klemann
Journal:  J Clin Med       Date:  2021-05-05       Impact factor: 4.241

  8 in total

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