Congenital biliary atresia: liver injury begins at birth

被引:23
作者
Makin, Erica [1 ]
Quaglia, Alberto [2 ]
Kvist, Nina [3 ]
Petersen, Bodil Laub [3 ]
Portmann, Bernard [2 ]
Davenport, Mark [1 ]
机构
[1] Kings Coll Hosp London, Dept Paediat Surg, London SE5 9RS, England
[2] Kings Coll Hosp London, Inst Liver Studies, London SE5 9RS, England
[3] Rigshosp, Dept Paediat Surg, DK-2100 Copenhagen, Denmark
关键词
Biliary atresia; Biliary atresia splenic malformation; Neonatal cholestasis; SPLENIC MALFORMATION SYNDROME; PROGNOSTIC SUBGROUP;
D O I
10.1016/j.jpedsurg.2008.10.069
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: The timing of onset of liver injury in biliary atresia (BA) is not known, although in approximately 10% of cases, biliary pathologic condition associated with the biliary atresia splenic malformation syndrome must begin well before birth. Methods: The study involved retrospective case-note review for infants with definite BA who underwent laparotomy within first week of life. Results: Three infants were identified who had occlusive BA evident on the first day of life. In all cases, their liver was grossly normal, and histologic changes were trivial. Conclusion: This suggests that the detrimental cholestatic liver injury, later characteristic of BA, only begins from the time of birth despite a prenatal occlusive biliary pathology. It may be that tissue injury only occurs with the onset of the perinatal bile surge initiating periductal bile leakage and the triggering of an inflammatory and ultimately fibrotic response. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:630 / 633
页数:4
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