[1] Muntean A, Davenport M. Biliary atresia & choledochal malformation--embryological and anatomical considerations[J]. Semin Pediatr Surg, 2022, 31(6):151235. [2] Zaben B A, Abualrub A M, Malhes W M, et al. Biliary atresia with rare associations: a case report and literature review[J]. Ann Med Surg (Lond), 2024, 86(11):6713-6716. [3] Yu P, Dong N, Pan Y K,et al. Ultrasonography is useful in differentiating between cystic biliary atresia and choledochal cyst[J]. Pediatr Surg Int, 2021, 37(6):731-736. [4] Ho A, Sacks M A, Sapra A, et al. The utility of gallbladder absence on ultrasound for children with biliary atresia[J]. Front Pediatr, 2021, 9:685268. [5] 付裕, 韩万斌, 向飞, 等. 多层螺旋CT与磁共振MRCP技术诊断胆总管结石价值分析[J]. 中国CT和MRI杂志,2022,20(1):119-121. [6] 杜森, 周青, 孙亮亮, 等. 多层螺旋CT联合血清LncRNA UCA1检测在胆囊癌中诊断价值[J]. 中国医学计算机成像杂志,2023,29(2):155-160. [7] 殷亮, 李章柱, 商明艳, 等. 比较3.0T与5.0T MR胆胰管造影图像质量[J]. 中国医学影像技术,2024,40(5):690-693. [8] Chen X, Zhao D, Ji H, et al. Predictive modeling for early detection of biliary atresia in infants with cholestasis: Insights from a machine learning study[J]. Comput Biol Med, 2024, 174:108439. [9] 杜森, 鲍志国, 周青. MSCT在原发性胆囊癌分期诊断及预后评估中的应用研究[J]. 中国CT和MRI杂志,2023,21(5):94-95. [10] Raţiu I, Lupuşoru R, Lungeanu D, et al. Diagnosis of malignant biliary obstruction: pondering over the ERCP, MRCP and histology[J]. J Int Med Res, 2022, 50(2):3000605221076924. [11] 姜璟, 汤悦, 朱叶, 等. 基于超声、肝胆核素显像和磁共振胆胰管成像影像学检查诊断 BA 准确性研究的系统评价和 Meta 分析[J]. 中国循证儿科杂志,2020,15(3) :166-176. [12] Kastenberg Z J, Deneau M R, O'Brien E A,et al. Fractionated bilirubin among 252 892 utah newborns with and without biliary atresia: a 15-year historical birth cohort study[J]. J Pediatr, 2023, 257:113339. [13] Nakamura H, Ara M, Koga H, et al. Duration from the first pale stool to portoenterostomy is prognostic in biliary atresia. Comparison with age at portoenterostomy[J]. Clin Res Hepatol Gastroenterol, 2021, 45(5):101584. [14] 陈敏霞, 李旭芳, 徐翼, 等. 140例胆道闭锁患儿临床特征分析[J]. 肝脏,2020,25(5):494-497. [15] Bove K E, Bernieh A, Picarsic J,et al. Hypoplasia of extrahepatic biliary tree and intrahepatic cholangiolopathy in cystic fibrosis imperfectly mimic biliary atresia in 4 infants with cystic fibrosis and kasai portoenterostomy[J]. Am J Surg Pathol, 2021, 45(11):1499-1508. [16] Liu S, Li T, Yang Q,et al. Biliary atresia: the development, pathological features, and classification of the bile duct[J]. Pediatr Surg Int, 2024, 40(1):42. [17] 胡玉杰, 肖婷, 项飞翔, 等. 超声在婴幼儿囊肿型胆道闭锁及胆总管囊肿鉴别诊断中的应用[J]. 中国医师杂志,2024,26(10):1456-1459. [18] Chen K, Zhang S, Cai D,et al. Clinical characteristics of choledochal cysts with intrahepatic bile duct dilatations: an observational study[J]. Ann Surg Treat Res, 2024, 106(4):225-230. [19] Chen Y T, Gao M J, Zheng Z B,et al. Comparative analysis of cystic biliary atresia and choledochal cysts[J]. Front Pediatr, 2022, 10:947876. [20] Verma A, Dhua A K, Kandasamy D,et al. Study of intrahepatic biliary architecture in patients operated for extrahepatic biliary atresia using magnetic resonance cholangiopancreatography[J]. J Indian Assoc Pediatr Surg, 2024, 29(1):23-27. [21] 宋斌, 赵厚亮, 叶莉. 三维磁共振胰胆管成像诊断小儿胆道闭锁价值分析[J]. 实用肝脏病杂志,2021,24(2):288-291. [22] 周宁, 张明杰, 缪定强, 等. 1.5T磁共振磁共振胰胆管造影术在诊断儿童胆道梗阻性疾病中的应用价值[J]. 实用医技杂志,2020,27(7):857-859. [23] Tajima T, Akai H, Sugawara H,et al. Breath-hold 3D magnetic resonance cholangiopancreatography at 1.5 T using a deep learning-based noise-reduction approach: comparison with the conventional respiratory-triggered technique[J]. Eur J Radiol, 2021, 144:109994. |