Literature DB >> 34524520

Comparison between cystic biliary atresia and choledochal cyst: a clinical controlled study.

Pu Yu1, Ning Dong2, Yong Kang Pan1, Long Li3.   

Abstract

PURPOSE: It is difficult to distinguish cystic biliary atresia (CBA) from choledochal cyst (CC) before intraoperative cholangiography in neonates or young infants because of the similar ultrasonographic patterns and clinical manifestations. This study is to investigate the difference of clinical parameters between CBA and CC.
METHODS: 96 patients with cyst at hepatic hilum whose ages were less than 120 days during the period from Jan'2013 to Nov'2015 were retrospectively studied, they were divided into CBA group and CC group by intraoperative cholangiography, there were 29 cases of CBA and 67 cases of CC. It was compared and analyzed on laboratory data, preoperative ultrasonographic features, intraoperative cholangiography and histopathological results between the two groups. Data were quoted as means ± standard deviation (SD) or median (range), Student's t test, non-parametric test and χ2 test were used as appropriate. P < 0.05 was considered as significant statistical difference.
RESULTS: CBA group and CC group were comparable for the operative age (51.76 ± 23.99 days vs. 50.03 ± 26.38 days, P = 0.76), weight (4.60 ± 0.75 kg vs. 4.44 ± 1.03 kg, P = 0.46) and sex proportion (M/F: 9/20 vs. 20/47, P = 0.91). there were significant differences (CBA vs. CC) in ALT [59(3-375) vs. 30 (6-247) IU/L, P < 0.001], AST [140(30-694) vs. 44(18-410) IU/L, P < 0.001], T-Bil [190 (107-326) vs.87(5-310) μmol/L, P < 0.001], D-Bil [85 (31-174) vs.14(1-122) μmol/L, P < 0.001] and TBA [112 (23-269) vs.9(1-337) μmol/L, P < 0.001]. There was insignificant statistical difference in GGT [332(112-2154) vs. 226(21-1810) IU/L, P = 0.099] between CBA group and CC group. The cyst size in CBA group was obviously smaller than CC group (the maximum longitudinal diameter: 2.52 ± 1.16 cm vs. 4.71 ± 2.23 cm, P < 0.001; the maximum transverse diameter: 1.64 ± 0.75 cm vs. 3.41 ± 1.79 cm, P < 0.001). Significant differences presented in preoperative ultrasonographic features and histopathological results between the two groups.
CONCLUSION: CBA should be suspected if ultrasonography indicates small cyst with characteristic manifestations of BA and elevated laboratory data. GGT was an insensitive indicator in distinguishing CBA from CC. Cholangiography should be done for the suspected CBA patients as soon as possible to confirm the diagnosis and have surgical intervention timely.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Choledochal cyst; Clinical parameters; Cystic biliary atresia; Ultrasonographic features

Mesh:

Year:  2021        PMID: 34524520     DOI: 10.1007/s00383-021-05004-y

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


  17 in total

1.  Diagnosis and management of biliary cystic malformations in neonates.

Authors:  Natsumi Tanaka; Takehisa Ueno; Yuichi Takama; Masahiro Fukuzawa
Journal:  J Pediatr Surg       Date:  2010-11       Impact factor: 2.545

2.  Postnatal management of prenatally diagnosed biliary cystic malformation.

Authors:  Hiromu Tanaka; Hideyuki Sasaki; Motoshi Wada; Tomoyuki Sato; Takuro Kazama; Kotaro Nishi; Hironori Kudo; Megumi Nakamura; Masaki Nio
Journal:  J Pediatr Surg       Date:  2014-12-05       Impact factor: 2.545

Review 3.  Anatomy and embryology of the biliary tract.

Authors:  Kara M Keplinger; Mark Bloomston
Journal:  Surg Clin North Am       Date:  2014-02-20       Impact factor: 2.741

4.  Clinical features differentiating biliary atresia from other causes of neonatal cholestasis.

Authors:  Way Seah Lee; Pei Fan Chai
Journal:  Ann Acad Med Singapore       Date:  2010-08       Impact factor: 2.473

5.  Biliary atresia: the King's College Hospital experience (1974-1995)

Authors:  M Davenport; N Kerkar; G Mieli-Vergani; A P Mowat; E R Howard
Journal:  J Pediatr Surg       Date:  1997-03       Impact factor: 2.545

6.  Antenatal presentation of biliary atresia.

Authors:  Rupert Hinds; Mark Davenport; Giorgina Mieli-Vergani; Nedim Hadzić
Journal:  J Pediatr       Date:  2004-01       Impact factor: 4.406

7.  Distinct Plasma Bile Acid Profiles of Biliary Atresia and Neonatal Hepatitis Syndrome.

Authors:  Kejun Zhou; Jun Wang; Guoxiang Xie; Ying Zhou; Weihui Yan; Weihua Pan; Yanran Che; Ting Zhang; Linda Wong; Sandi Kwee; Yongtao Xiao; Jie Wen; Wei Cai; Wei Jia
Journal:  J Proteome Res       Date:  2015-10-16       Impact factor: 4.466

Review 8.  Biliary atresia.

Authors:  Jane L Hartley; Mark Davenport; Deirdre A Kelly
Journal:  Lancet       Date:  2009-11-14       Impact factor: 79.321

9.  Gamma-glutamyl transferase in the diagnosis of biliary atresia.

Authors:  Kuo-Shu Tang; Li-Tung Huang; Ying-Hsien Huang; Chi-Yin Lai; Chi-Hung Wu; Sheng-Ming Wang; Kao-Pin Hwang; Fu-Chen Huang; Mao-Meng Tiao
Journal:  Acta Paediatr Taiwan       Date:  2007 Jul-Aug

10.  Elevated bile acids in newborns with Biliary Atresia (BA).

Authors:  Kejun Zhou; Na Lin; Yongtao Xiao; Yang Wang; Jie Wen; Gang-Ming Zou; Xuefan Gu; Wei Cai
Journal:  PLoS One       Date:  2012-11-14       Impact factor: 3.240

View more
  1 in total

Review 1.  Biliary Atresia: Clinical Phenotypes and Aetiological Heterogeneity.

Authors:  Mark Davenport; Ancuta Muntean; Nedim Hadzic
Journal:  J Clin Med       Date:  2021-12-01       Impact factor: 4.241

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.