An Unusual Case of Trisomy 18 Associated with Paucity of Bile Ducts

被引:5
|
作者
Kahramaner, Zelal [1 ]
Erdemir, Aydin [1 ]
Cosar, Hese [1 ]
Turkoglu, Ebru [1 ]
Sutcuoglu, Sumer [1 ]
Turelik, Ozlem [2 ]
Cumurcu, Suheyla [2 ]
Bayol, Umit [2 ]
Ozer, Esra [1 ]
机构
[1] Izmir Tepecik Res & Teaching Hosp, Dept Pediat, Div Neonatol, Minist Hlth, Izmir, Turkey
[2] Izmir Tepecik Res & Teaching Hosp, Dept Pathol, Minist Hlth, Izmir, Turkey
关键词
chromosomal disorders; edward's syndrome; trisomy; 18; paucity of intrahepatic bile duct; SURVIVAL; INFANCY;
D O I
10.3109/15513815.2013.768736
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
A case of neonatal cholestasis associated with Trisomy 18 (Edward's syndrome) is presented. A 3-day-old boy was referred to our clinic due to respiratory distress, elevated serum direct bilirubin levels, a systolic heart murmur, growth restriction and micrognathia. Liver biopsy and chromosomal analysis revealed paucity of intrahepatic bile ducts and Trisomy 18. Extrahepatic biliary atresia was reported in only a few patients with Trisomy 18. To our knowledge, we described for the first time a patient with Trisomy 18 and neonatal cholestasis associated with paucity of interlobular bile ducts.
引用
收藏
页码:337 / 340
页数:4
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