[1] Ndoye NA, Welle IB, Cisse L, et al. Choledochal cyst in children in Dakar: Diagnostic and therapeutic aspects. Afr J Paediatr Surg, 2021, 18(3): 168-170. [2] Friedmacher F, Ford KE, Davenport M. Choledochal malformations: global research, scientific advances and key controversies. Pediatr Surg Int, 2019, 35(3): 273-282. [3] Zhu L, Xiong J, Lyu Z, et al. Type C pancreaticobiliary maljunction is associated with perforated choledochal cyst in children. Front Pediatr, 2020, 8: 168. [4] Cao J, Wang L, Zou X. Coexistence of complete pancreas divisum and anomalous pancreaticobiliary junction in a patient with type IA choledochal cyst. Clin Gastroenterol Hepatol, 2019, 17(12): A27-A8. [5] Qu X, Cui L, Xu J. Laparoscopic surgery in the treatment of children with choledochal Cyst. Pak J Med Sci, 2019, 35(3): 807-811. [6] Nguyen HV, Do DH, Nguyen HV, et al. Treatment of complex complications after choledochal cyst resection by multiple minimal invasive therapies: A case report. Int J Surg Case Rep, 2020, 73: 130-133. [7] Sugezawa K, Murawaki Y, Sakamoto T, et al. Gallbladder cancer with biliary intraepithelial neoplasia complicated by pancreaticobiliary maljunction: A case report. Yonago Acta Med, 2022, 65(1): 101-105. [8] Cochran ED, Lazow SP, Kim AG, et al. The in-utero diagnosis of choledochal cyst: can postnatal imaging predict benefit from early surgical intervention? J Matern Fetal Neonatal Med, 2022, 35(6): 1070-1074. [9] Akanni DWMM, N'zi KP, Savi de Tové KM, et al. Contribution of imaging in the diagnosis of cholangiocarcinoma in choledochal cyst. Case Rep Radiol, 2018, 2018: 8346232. [10] Kim YJ, Kim SH, Yoo SY, et al. Comparison of clinical and radiologic findings between perforated and non-perforated choledochal cysts in children. Korean J Radiol, 2022, 23(2): 271-279. [11] Diao M, Li L, Cheng W. Laparoscopic management for aberrant hepatic duct in children with choledochal cysts. Surg Endosc, 2019, 33(7): 2376-2380. [12] Ishii J, Miyano G, Takahashi T, et al. Oncologic safety of carrel patch hepaticojejunostomy for treating cystic-type choledochal cyst in children based on 20-plus years follow-up. Pediatr Surg Int, 2022, 39(1):65. [13] Kowalski A, Kowalewski G, Kaliciński P, et al. Choledochal cyst excision in infants-A retrospective study. Children (Basel), 2023, 10(2):373. [14] Ramachandran A, Srivastava DN, Gupta AK, et al. The double trouble: A case of duplicated extrahepatic bile duct with choledochal cyst. Indian J Pediatr, 2019, 86(2): 186-188. [15] Oh C, Cheun JH, Kim HY. Clinical comparison between the presence and absence of protein plugs in pediatric choledochal cysts: experience in 390 patients over 30 years in a single center. Ann Surg Treat Res, 2021, 101(5): 306-313. [16] Meldrum JT, Tabak BD, Roberts CA, et al. Complex pancreaticobiliary maljunction with pancreas divisum and obstructive pseudocyst. J Clin Imaging Sci, 2020, 10: 31. [17] Ma Y, Lu L, Tan K, et al. Reduced peroxisome proliferator-activated receptor-alpha and bile acid nuclear receptor NR1H4/FXR may affect the hepatic immune microenvironment of biliary atresia. Front Immunol, 2022, 13: 875593. [18] Kronfli R, Davenport M. Insights into the pathophysiology and classification of type 4 choledochal malformation. J Pediatr Surg, 2020, 55(12): 2642-2646. [19] Hill R, Parsons C, Farrant P, et al. Intrahepatic duct dilatation in type 4 choledochal malformation: pressure-related, postoperative resolution. J Pediatr Surg, 2011, 46(2):299-303. |