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先天性胆管闭锁中的肝内胆管囊肿

Intrahepatic biliary cysts in congenital biliary atresia.

作者信息

Fain J S, Lewin K J

机构信息

Department of Pathology, UCLA Medical Center 90024-1732.

出版信息

Arch Pathol Lab Med. 1989 Dec;113(12):1383-6.

PMID:2589950
Abstract

A case of pronounced cystic dilatation of the intrahepatic bile ducts with biliary atresia is presented. Intrahepatic biliary cysts have been described in biliary atresia, although, as far as we are aware, none as extensive as in this case. The cysts represent end-stage obstruction with irreversible liver injury; thus, drainage of these cysts does not alleviate the condition. The differential diagnosis includes Caroli's disease, congenital hepatic fibrosis, and polycystic liver disease.

摘要

本文报告一例肝内胆管显著囊性扩张合并胆道闭锁的病例。肝内胆管囊肿在胆道闭锁中已有报道,尽管据我们所知,尚无如此广泛的病例。这些囊肿代表了终末期梗阻伴不可逆性肝损伤;因此,引流这些囊肿并不能缓解病情。鉴别诊断包括卡罗里病、先天性肝纤维化和多囊肝疾病。

相似文献

1
Intrahepatic biliary cysts in congenital biliary atresia.先天性胆管闭锁中的肝内胆管囊肿
Arch Pathol Lab Med. 1989 Dec;113(12):1383-6.
2
Congenital cystic dilatation of the intrahepatic bile ducts (Caroli's disease): report of a case and review of the literature.先天性肝内胆管囊状扩张症(卡罗里病):1例报告并文献复习
Surgery. 1979 May;85(5):589-92.
3
[Role of liver biopsy in the diagnosis of prolonged cholestasis in infants].[肝活检在婴儿长期胆汁淤积症诊断中的作用]
Rev Invest Clin. 1992 Apr-Jun;44(2):193-202.
4
A peculiar form of multiple cystic dilatation of the intrahepatic biliary system found in a patient with biliary atresia.在一名胆道闭锁患者中发现的肝内胆管系统的一种特殊形式的多发性囊性扩张。
J Pediatr Surg. 1997 Dec;32(12):1776-9. doi: 10.1016/s0022-3468(97)90533-9.
5
Congenital biliary dilatation in autosomal dominant adult polycystic disease of the liver and kidneys.常染色体显性遗传性成人多囊肝和多囊肾中的先天性胆管扩张
Arch Pathol Lab Med. 1988 Nov;112(11):1113-6.
6
[Congenital cystic dilatation of the intrahepatic bile ducts. Caroli's disease and its complications].
Schweiz Med Wochenschr. 1979 May 19;109(20):758-62.
7
[Hepatocholedochal cyst with congenital segmental dilatation of the intrahepatic bile ducts (Caroli's disease) and portal hypertension].
Lyon Chir. 1971 Jul-Aug;67(4):299-301.
8
Polycystic kidney rat is a novel animal model of Caroli's disease associated with congenital hepatic fibrosis.多囊肾大鼠是一种与先天性肝纤维化相关的卡罗里病的新型动物模型。
Am J Pathol. 2001 May;158(5):1605-12. doi: 10.1016/S0002-9440(10)64116-8.
9
MR imaging of biliary cysts in children with biliary atresia: clinical associations and pathologic correlation.胆道闭锁患儿胆管囊肿的磁共振成像:临床关联与病理相关性
AJR Am J Roentgenol. 1994 Jan;162(1):167-71. doi: 10.2214/ajr.162.1.8273658.
10
Association of carcinoma with congenital cystic conditions of the liver and bile ducts.癌与肝脏和胆管先天性囊性疾病的关联。
Am J Gastroenterol. 1977 Jan;67(1):40-6.

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Immunology of Biliary Atresia.胆道闭锁的免疫学
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胆道闭锁:病理学、病因学与发病机制
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Impact of ductal plate malformation on survival with native liver in children with biliary atresia.胆管板畸形对胆道闭锁患儿自体肝生存的影响。
Pediatr Surg Int. 2015 Sep;31(9):837-43. doi: 10.1007/s00383-015-3728-6. Epub 2015 Jul 4.
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Biliary atresia: recent progress.胆道闭锁:近期进展
J Clin Gastroenterol. 2008 Jul;42(6):720-9. doi: 10.1097/MCG.0b013e3181646730.
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Histological assessment of bile lake formation after hepatic portoenterostomy for biliary atresia.先天性胆道闭锁肝门肠吻合术后胆汁湖形成的组织学评估。
Pediatr Surg Int. 2008 Mar;24(3):265-9. doi: 10.1007/s00383-007-2099-z. Epub 2007 Dec 20.