Diffuse-Type Caroli Disease with Characteristic Central Dot Sign Complicated by Multiple Intrahepatic and Common Bile Duct Stones
0
조회
0
다운로드
0
인용
0
참고문헌
키워드
초록
Caroli disease (CD) is a rare congenital malformation of the liver characterized by non-obstructive, segmental, cystic dilatation of the intrahepatic bile ducts (IHDs). The clinical course is usually asymptomatic for the first 5–20 years, and symptoms may seldom occur throughout the patient’s life. Bile stagnation leads to recurrent episodes of cholangitis, stone formation, or liver abscesses, and biliary cirrhosis usually occurs years later. Here we report on a 42-year-old man diagnosed with diffuse-type CD with a characteristic central dot sign, who had multiple intrahepatic and common bile duct (CBD) stones. CBD stones were treated successfully with endoscopic retrograde cholangiopancreatography (ERCP).
Abstract
Caroli disease (CD) is a rare congenital malformation of the liver characterized by non-obstructive, segmental, cystic dilatation of the intrahepatic bile ducts (IHDs). The clinical course is usually asymptomatic for the first 5–20 years, and symptoms may seldom occur throughout the patient’s life. Bile stagnation leads to recurrent episodes of cholangitis, stone formation, or liver abscesses, and biliary cirrhosis usually occurs years later. Here we report on a 42-year-old man diagnosed with diffuse-type CD with a characteristic central dot sign, who had multiple intrahepatic and common bile duct (CBD) stones. CBD stones were treated successfully with endoscopic retrograde cholangiopancreatography (ERCP).
참고문헌 (20)
- Caroli J, "A new disease, undoubtedly congenital, of the bile ducts: unilobar cystic dilation of the hepatic ducts", Sem Hop, 34, pp.496~502 (1958)
- Giovanardi RO, "Monolobar Caroli’s disease in an adult. Case report", Hepatogastroenterology, 50, pp.2185~2187 (2003)
- Pezzilli R, "Education and imaging. Hepatobiliary and pancreatic: Caroli’s disease", J Gastroenterol Hepatol, 23, pp.1621~ (2008)
- Gupta AK, "Caroli’s disease", Indian J Pediatr, 73, pp.233~235 (2006)
- Levy AD, "Caroli’s disease:radiologic spectrum with pathologic correlation", AJR Am J Roentgenol, 179, pp.1053~1057 (2002)
- Desmet VJ, "Ludwig symposium on biliary disorders--part I. Pathogenesis of ductal plate abnormalities", Mayo Clin Proc, 73, pp.80~89 (1998)
- Yonem O, "Clinical characteristics of Caroli’s disease", World J Gastroenterol, 13, pp.1930~1933 (2007)
- 채영제, "대장암 및 다낭종신과 동반된 Caroli병 1예", Clinical Endoscopy, 32(1), pp.71~74 (2006), 대한소화기내시경학회
- Wang ZX, "Clinical classification of Caroli’s disease:an analysis of 30 patients", HPB (Oxford), 17, pp.278~283 (2015)
- Bockhorn M, "The role of surgery in Caroli’s disease", J Am Coll Surg, 202, pp.928~932 (2006)
- Chapman RW, "Risk factors for biliary tract carcinogenesis", Ann Oncol, 10(Suppl 4), pp.308~311 (1999)
- Dayton MT, "Caroli’s disease: a premalignant condition?", Am J Surg, 145, pp.41~48 (1983)
- Totkas S, "Cholangiocellular carcinoma associated with segmental Caroli’s disease", Eur J Surg Oncol, 26, pp.520~521 (2000)
- Shimonishi T, "Precancerous lesions of intrahepatic cholangiocarcinoma", J Hepatobiliary Pancreat Surg, 7, pp.542~550 (2000)
- Lall NU, "Caroli disease and the central dot sign", Pediatr Radiol, 39, pp.754~ (2009)
- Chung EM, "From the radiologic pathology archives: pediatric polycystic kidney disease and other ciliopathies: radiologic-pathologic correlation", Radiographics, 34, pp.155~178 (2014)
- Sinakos E, "The clinical presentation of von Meyenburg complexes", Hippokratia, 15, pp.170~173 (2011)
- Ros E, "Ursodeoxycholic acid treatment of primary hepatolithiasis in Caroli’s syndrome", Lancet, 342, pp.404~406 (1993)
- 구대회, "Caroli’s disease misdiagnosed as intraductal papillary neoplasm of the bile duct", Clinical and Molecular Hepatology, 21(2), pp.175~179 (2015), 대한간학회
- Ulrich F, "Therapy of Caroli’s disease by orthotopic liver transplantation", Transplant Proc, 34, pp.2279~2280 (2002)
