An Atypical Presentation of Alagille Syndrome

被引:7
作者
Wu, Katherine Y. [1 ]
Treece, Amanda L. [2 ]
Russo, Pierre A. [3 ]
Wen, Jessica W. [4 ]
机构
[1] Childrens Hosp Philadelphia, Dept Pediat, Philadelphia, PA 19104 USA
[2] Childrens Hosp Colorado, Dept Pathol & Lab Med, Aurora, CO USA
[3] Childrens Hosp Philadelphia, Div Anat Pathol, Philadelphia, PA 19104 USA
[4] Childrens Hosp Philadelphia, Div Gastroenterol Hepatol & Nutr, Philadelphia, PA 19104 USA
关键词
Alagille syndrome; cholestasis; CK7; JAG1; jaundice; CHOLEDOCHAL CYSTS; JAG1; MUTATIONS; CHOLESTASIS; DIAGNOSIS; FEATURES; PAUCITY;
D O I
10.1177/1093526616686902
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Alagille syndrome is a multisystem disorder classically involving the liver, heart, vertebrae, facial features, and the eyes. In this case report, we document a case of Alagille syndrome with an atypical clinical and histopathologic presentation and subsequent identification of a novel JAG1 missense mutation. This case highlights that there may be both atypical clinical and pathologic findings in mutation-proven Alagille syndrome and that the diagnosis of Alagille syndrome should be considered in cases of ongoing bile duct damage in the setting of early-onset jaundice, cholestasis, hepatosplenomegaly, posterior embryotoxon in the eyes, and butterfly vertebrae.
引用
收藏
页码:79 / 83
页数:5
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