期刊
PEDIATRICS
卷 117, 期 3, 页码 E596-E600出版社
AMER ACAD PEDIATRICS
DOI: 10.1542/peds.2005-1411
关键词
congenital abnormalities; liver disease; prenatal diagnosis
类别
Familial choledochal cysts are extremely rare. High-resolution ultrasound now allows for the antenatal diagnosis of these anomalies. After delivery, elective surgical resection should be planned; however, increases in size, deterioration of liver function, and ascending cholangitis frequently force early intervention. We report an unusual occurrence of siblings with type I choledochal cysts and review the existing literature on cause, genetics, classification, diagnosis, and management of this disease.
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