Literature DB >> 32868669

Segmental Atrophy of Explanted Livers in Biliary Atresia: Pathological Data From 63 Cases of Failed Portoenterostomy.

Kenji Santo1,2, Noriyuki Nakano1, Mureo Kasahara3, Seisuke Sakamoto3, Akinari Fukuda3, Yutaka Kanamori4, Akihiro Fujino4, Masaki Horiike2, Toshihiko Shibata2, Toshihiro Muraji5, Takako Yoshioka1.   

Abstract

OBJECTIVES: Atrophy of the left lateral segment (LLS) is often encountered in liver transplantation (LT) for biliary atresia (BA). To clarify the meaning of the heterogeneous atrophy, we compared the pathological characteristics of the LLS with the right posterior segment (RPS) of BA livers obtained during LT.
METHODS: Among the 116 patients with BA who underwent LT at our hospital between 2014 and 2018, 63 patients with persistent cholestasis after the Kasai portoenterostomy (KP) were selected. Three pathologists evaluated tissues from the LLS and RPS for 5 pathological parameters. Positive areas in whole-slide image observed as portal inflammation, fibrosis, cholestasis, and ductular reaction, were analyzed with automated image quantitation. Moreover, we examined the relationship between the pathological score and the Pediatric End-stage Liver Disease (PELD) score.
RESULTS: The median age at LT was 7 months (range 4-26 months). Inflammation and fibrosis were significantly greater in the LLS than in the RPS (P < 0.001, for both); however, there were no differences in cholestasis, ductular reaction, and hepatocellular damage (P = 0.3, 0.3, and 0.82). The same results were obtained in automated image quantitation. Moreover, the sums of the 5 pathological scores in the LLS showed a significant positive correlation with the PELD score (P = 0.016, rs = 0.3).
CONCLUSIONS: More severe inflammation and fibrosis without cholestasis were observed in the LLS. The segmental atrophy may not be associated with poor bile drainage, but with etiopathogenesis of BA. Moreover, the proper site for biopsy during KP could be the LLS.
Copyright © 2020 by European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition.

Entities:  

Mesh:

Year:  2021        PMID: 32868669     DOI: 10.1097/MPG.0000000000002929

Source DB:  PubMed          Journal:  J Pediatr Gastroenterol Nutr        ISSN: 0277-2116            Impact factor:   2.839


  5 in total

1.  Diagnosis of liver cirrhosis with two-dimensional shear wave elastography in biliary atresia before Kasai portoenterostomy.

Authors:  Cailin Ding; Zengmeng Wang; Chunhui Peng; Wenbo Pang; Sarah Siyin Tan; Yajun Chen
Journal:  Pediatr Surg Int       Date:  2021-11-30       Impact factor: 1.827

2.  Selective enlargement of left lateral segment liver volume as a potential diagnostic predictor for biliary atresia.

Authors:  Kenji Santo; Yuichi Takama; Yuki Hirose; Jun Matsui; Ririko Takemura; Kei Nakada; Takashi Sasaki
Journal:  Pediatr Surg Int       Date:  2022-09-15       Impact factor: 2.003

Review 3.  Peri-Operative Liver Fibrosis and Native Liver Survival in Pediatric Patients with Biliary Atresia: A Systematic Review and Meta-Analysis.

Authors:  Ashkan Jahangirnia; Irina Oltean; Youssef Nasr; Nayaar Islam; Arielle Weir; Joseph de Nanassy; Ahmed Nasr; Dina El Demellawy
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2022-09-05

4.  New insights in understanding biliary atresia from the perspectives on maternal microchimerism.

Authors:  Toshihiro Muraji; Ryuta Masuya; Toshio Harumatsu; Takafumi Kawano; Mitsuru Muto; Satoshi Ieiri
Journal:  Front Pediatr       Date:  2022-09-23       Impact factor: 3.569

5.  Circulating maternal chimeric cells have an impact on the outcome of biliary atresia.

Authors:  Ryuta Masuya; Toshihiro Muraji; Sami B Kanaan; Toshio Harumatsu; Mitsuru Muto; Miki Toma; Toshihiro Yanai; Anne M Stevens; J Lee Nelson; Kazuhiko Nakame; Atsushi Nanashima; Satoshi Ieiri
Journal:  Front Pediatr       Date:  2022-09-20       Impact factor: 3.569

  5 in total

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