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Regression of antenatally diagnosed localized Caroli's disease.

作者信息

Bratu I, Laberge J M, Khalifé S, Sinsky A

机构信息

Division of Pediatric Surgery, The Montreal Children's Hospital, Quebec, Canada.

出版信息

J Pediatr Surg. 2000 Sep;35(9):1390-3. doi: 10.1053/jpsu.2000.9349.

DOI:10.1053/jpsu.2000.9349
PMID:10999710
Abstract

The authors report on an infant who had a multiloculated cystic lesion located in segment IV of the liver, consistent with Caroli's disease diagnosed, by routine prenatal ultrasound at 25 weeks' gestation, and confirmed by hepatobiliary HIDA scan and computed tomography soon after birth. Because there was no sign of biliary obstruction, the patient was observed initially, with gradual regression of the cysts noted by serial sonograms. Caroli's disease in older children and adults often is associated with recurrent cholangitis and cirrhosis, mandating resection when the disease is unilobar. However, the natural history of Caroli's disease diagnosed in utero is unclear, and a period of observation appears warranted in the asymptomatic patient.

摘要

相似文献

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Regression of antenatally diagnosed localized Caroli's disease.
J Pediatr Surg. 2000 Sep;35(9):1390-3. doi: 10.1053/jpsu.2000.9349.
2
Caroli's disease: prenatal diagnosis, postnatal outcome and genetic analysis.卡罗里病:产前诊断、产后结局及基因分析
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Intern Med. 2016;55(20):3009-3012. doi: 10.2169/internalmedicine.55.6818. Epub 2016 Oct 15.
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An unusual choledochal cyst.
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Caroli's disease and congenital hepatic fibrosis associated with polycystic kidney disease. A case presenting with acute focal bacterial nephritis.卡罗里病及先天性肝纤维化合并多囊肾病。1例表现为急性局灶性细菌性肾炎的病例。
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