Literature DB >> 23064804

A morphological study of the removed livers from patients receiving living donor liver transplantation for adult biliary atresia.

Toshiharu Matsuura1, Kenichi Kohashi, Yusuke Yanagi, Isamu Saeki, Makoto Hayashida, Shinichi Aishima, Yoshinao Oda, Tomoaki Taguchi.   

Abstract

BACKGROUND: In liver transplantation (LT) for adult biliary atresia (BA), we often encounter a cirrhotic deformation of the native liver. We aimed to investigate a morphological study of the removed livers and the patient's clinical status.
METHODS: We examined 8 BA patients who had undergone LT in adulthood at our hospital. The presence of hypertrophic or atrophic areas of the removed liver was recorded macroscopically. We graded the microscopic findings in the porta hepatis area, a hypertrophic area, and an atrophic area, respectively. Moreover, we investigated the relationship between these morphological findings and the pre-transplant clinical status (MELD score).
RESULTS: Macroscopically, a hypertrophic area existed in central liver in all cases (8/8 cases), while an atrophic area was existed in peripheral liver (7/8 cases). Microscopically, an atrophic area was the most severely impaired, while the porta hepatis and hypertrophic area were relatively intact. The pathological score in a compensatory hypertrophic area was strongly correlated with the MELD score.
CONCLUSIONS: This study suggests that the partial shrinking is not uncommon in BA cirrhotic liver. It may be due to the imbalance of bile drainage by the different segment. The patient's pre-transplant status depends on the compensatory hypertrophic liver.

Entities:  

Mesh:

Year:  2012        PMID: 23064804     DOI: 10.1007/s00383-012-3183-6

Source DB:  PubMed          Journal:  Pediatr Surg Int        ISSN: 0179-0358            Impact factor:   1.827


  13 in total

1.  Clinicopathological study of a hilar nodule in the livers of long-term survivors with biliary atresia.

Authors:  R Ijiri; Y Tanaka; K Kato; K Misugi; Y Ohama; M Shinkai; T Nishi; N Aida; F Kondo
Journal:  Pathol Int       Date:  2001-01       Impact factor: 2.534

2.  MELD and PELD: application of survival models to liver allocation.

Authors:  R H Wiesner; S V McDiarmid; P S Kamath; E B Edwards; M Malinchoc; W K Kremers; R A Krom; W R Kim
Journal:  Liver Transpl       Date:  2001-07       Impact factor: 5.799

3.  The anatomic pattern of biliary atresia identified at time of Kasai hepatoportoenterostomy and early postoperative clearance of jaundice are significant predictors of transplant-free survival.

Authors:  Riccardo Superina; John C Magee; Mary L Brandt; Patrick J Healey; Greg Tiao; Fred Ryckman; Frederick M Karrer; Kishore Iyer; Annie Fecteau; Karen West; R Cartland Burns; Alan Flake; Hanmin Lee; Jeff A Lowell; Pat Dillon; Paul Colombani; Richard Ricketts; Yun Li; Jeffrey Moore; Kasper S Wang
Journal:  Ann Surg       Date:  2011-10       Impact factor: 12.969

4.  A new hepatic portoenterostomy with division of the ligamentum venosum for treatment of biliary atresia: a preliminary report.

Authors:  H Ando; T Seo; F Ito; K Kaneko; Y Watanabe; T Harada; T Ito
Journal:  J Pediatr Surg       Date:  1997-11       Impact factor: 2.545

5.  Reappraising the portoenterostomy procedure according to sound physiologic/anatomic principles enhances postoperative jaundice clearance in biliary atresia.

Authors:  Hiroki Nakamura; Hiroyuki Koga; Momoko Wada; Go Miyano; Rafael Dizon; Yoshifumi Kato; Geoffrey J Lane; Tadaharu Okazaki; Atsuyuki Yamataka
Journal:  Pediatr Surg Int       Date:  2012-02       Impact factor: 1.827

6.  Liver and portal histopathological correlation with age and survival in extra hepatic biliary atresia.

Authors:  Shilpa Sharma; Prasenjit Das; S Dattagupta; Lalit Kumar; Devendra K Gupta
Journal:  Pediatr Surg Int       Date:  2011-05       Impact factor: 1.827

7.  Kasai portoenterostomy--new insights from hepatic morphology.

Authors:  Ali Hussein; Judy Wyatt; Ashley Guthrie; Mark D Stringer
Journal:  J Pediatr Surg       Date:  2005-02       Impact factor: 2.545

8.  The therapy of biliary atresia combining the Kasai portoenterostomy with liver transplantation: a single center experience.

Authors:  J P Vacanti; R C Shamberger; A Eraklis; C W Lillehei
Journal:  J Pediatr Surg       Date:  1990-01       Impact factor: 2.545

Review 9.  Biliary atresia.

Authors:  R Ohi; M Ibrahim
Journal:  Semin Pediatr Surg       Date:  1992-05       Impact factor: 2.754

10.  Long-term outcome of children with biliary atresia who were not transplanted after the Kasai operation: >20-year experience at a children's hospital.

Authors:  Masato Shinkai; Youkatsu Ohhama; Hiroshi Take; Norihiko Kitagawa; Hironori Kudo; Kyoko Mochizuki; Tomoko Hatata
Journal:  J Pediatr Gastroenterol Nutr       Date:  2009-04       Impact factor: 2.839

View more
  4 in total

Review 1.  Maternal microchimerism in biliary atresia: are maternal cells effector cells, targets, or just bystanders?

Authors:  Toshihiro Muraji
Journal:  Chimerism       Date:  2014-03-26

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

Review 3.  Unique manifestations of biliary atresia provide new immunological insight into its etiopathogenesis.

Authors:  Toshihiro Muraji; Haruo Ohtani; Satoshi Ieiri
Journal:  Pediatr Surg Int       Date:  2017-10-11       Impact factor: 1.827

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

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.