[1] |
Friedmacher F, Ford KE, Davenport M. Choledochal malformations: global research, scientific advances and key controversies[J]. Pediatr Surg Int, 2019, 35(3):273-282.
|
[2] |
Katabathina VS, Kapalczynski W, Dasyam AK, et al. Adult choledochal cysts: current update on classification, pathogenesis, and cross-sectional imaging findings[J]. Abdom Imaging, 2015, 40(6): 1971-1981.
|
[3] |
Wong JK, Campbell D, Ngo ND, et al. Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes[J]. BMC Med Genomics, 2016, 9(1):75.
|
[4] |
Kotalova R, Dusatkova P, Drabova J, et al. Choledochal cyst with 17q12 chromosomal duplication[J]. Ann Hum Genet, 2018, 82(1): 48-51.
|
[5] |
Hwang HS, Kim MJ, Lee SS, et al. Smooth muscle distribution patterns of choledochal cysts and their implications for pathogenesis and postoperative complications[J]. Am J Clin Pathol, 2020, 153(6): 760-771.
|
[6] |
Madadi-Sanjani O, Wirth TC, Kuebler JF, et al. Choledochal cyst and malignancy: a plea for lifelong follow-up[J]. Eur J Pediatr Surg, 2019, 29(2):143-149.
|
[7] |
李斌, 邱智泉, 刘辰, 等. 改进外科治疗策略规避Ⅰ型和Ⅳ型先天性胆管囊肿术后并发症[J].中华肝胆外科杂志, 2016, 22(12): 848-851.
|
[8] |
Søreide K, Søreide JA. Bile duct cyst as precursor to biliary tract cancer[J]. Ann Surg Oncol, 2007, 14(3):1200-1211.
|
[9] |
Baison GN, Bonds MM, Helton WS, et al. Choledochal cysts: similarities and differences between Asian and Western countries[J]. World J Gastroenterol, 2019, 25(26):3334-3343.
|
[10] |
Soares KC, Goldstein SD, Ghaseb MA, et al. Pediatric choledochal cysts: diagnosis and current management[J]. Pediatr Surg Int, 2017, 33(6):637-650.
|
[11] |
Ronnekleiv-Kelly SM, Soares KC, Ejaz A, et al. Management of choledochal cysts[J]. Curr Opin Gastroenterol, 2016, 32(3):225-231.
|
[12] |
Todani T, Watanabe Y, Narusue M, et al. Congenital bile duct cysts: classification, operative procedures, and review of thirty-seven cases including cancer arising from choledochal cyst[J]. Am J Surg, 1977, 134(2):263-269.
|
[13] |
Todani T, Watanabe Y, Toki A, et al. Classification of congenital biliary cystic disease: special reference to type Ic and IVA cysts with primary ductal stricture[J]. J Hepatobiliary Pancreat Surg, 2003, 10(5):340-344.
|
[14] |
李斌, 邱智泉, 姜小清, 等. 计划性肝切除在"中央型"肝内外胆管囊肿治疗中的应用[J]. 中华肝胆外科杂志, 2017, 23(9):619-623.
|
[15] |
Sgro M, Rossetti S, Barozzino T, et al. Caroli's disease: prenatal diagnosis, postnatal outcome and genetic analysis[J]. Ultrasound Obstet Gynecol, 2004, 23(1):73-76.
|
[16] |
Torra R, Badenas C, Darnell A, et al. Autosomal dominant polycystic kidney disease with anticipation and Caroli's disease associated with a PKD1 mutation. rapid communication[J]. Kidney Int, 1997, 52(1): 33-38.
|
[17] |
De Jesus-Rojas W, McBeth K, Yadav A, et al. Severe hepatopulmonary syndrome in a child with Caroli syndrome[J]. Case Rep Pediatr, 2017: 2171974.
|
[18] |
Kumar A, Akselrod D, Prikis M. Caroli disease revisited: a case of a kidney transplant patient with autosomal polycystic kidney disease and recurrent episodes of cholangitis[J]. Transplant Proc, 2019, 51(2):541-544.
|
[19] |
Romine MM, White J. Role of transplant in biliary disease[J]. Surg Clin North Am, 2019, 99(2):387-401.
|