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A history of the Kasai operation: hepatic portoenterostomy for biliary atresia.

作者信息

Ohi R

出版信息

World J Surg. 1988 Dec;12(6):871-4. doi: 10.1007/BF01655504.

DOI:10.1007/BF01655504
PMID:3074594
Abstract
摘要

相似文献

1
A history of the Kasai operation: hepatic portoenterostomy for biliary atresia.Kasai手术史:用于胆道闭锁的肝门肠吻合术。
World J Surg. 1988 Dec;12(6):871-4. doi: 10.1007/BF01655504.
2
The sensei of Sendai: correcting the uncorrectable.仙台的宗师:纠正不可纠正之事。
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3
50 Years Ago in TheJournal ofPediatrics: Extrahepatic Biliary Atresia: Comments on the Frequency of Potentially Operable Cases.50年前发表于《儿科学杂志》:肝外胆道闭锁:关于潜在可手术病例发生率的评论
J Pediatr. 2016 Jul;174:246. doi: 10.1016/j.jpeds.2016.01.047.
4
50 Years Ago in The Journal of Pediatrics: Primary Liver Cell Carcinoma Associated with Biliary Cirrhosis Due to Congenital Bile Duct Atresia.50年前发表于《儿科学杂志》:原发性肝细胞癌与先天性胆管闭锁所致胆汁性肝硬化相关。
J Pediatr. 2015 Jul;167(1):63. doi: 10.1016/j.jpeds.2014.12.073.
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Effect of repeat Kasai hepatic portoenterostomy on pediatric live-donor liver graft for biliary atresia.重复凯氏肝门肠吻合术对小儿活体供肝肝移植治疗胆道闭锁的影响。
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6
The treatment of biliary atresia in Europe 1969-1995.1969 - 1995年欧洲胆管闭锁的治疗
Tohoku J Exp Med. 1997 Jan;181(1):75-83. doi: 10.1620/tjem.181.75.
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Early detection of biliary atresia: past, present & future.先天性胆道闭锁的早期检测:过去、现在与未来。
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Kasai portoenterostomy--new insights from hepatic morphology.肝门空肠吻合术——肝脏形态学的新见解
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[Follow up for a cohort of patients with biliary atresia: late surgery and development of biliary cysts].[一组胆道闭锁患者的随访:延迟手术与胆囊肿的发展]
Rev Chil Pediatr. 2017;88(5):629-634. doi: 10.4067/S0370-41062017000500009.

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Surg Case Rep. 2025;11(1). doi: 10.70352/scrj.cr.25-0209. Epub 2025 May 28.
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[Kasai-hepatoportoenterostomy for the treatment of biliary atresia - What is important?].[用于治疗胆道闭锁的Kasai肝门肠吻合术 - 要点是什么?]
Chirurgie (Heidelb). 2025 Jun;96(6):474-481. doi: 10.1007/s00104-025-02259-2. Epub 2025 Feb 27.
3
Biliary atresia.

本文引用的文献

1
THE SURGERY OF INFANTILE OBSTRUCTIVE JAUNDICE.小儿梗阻性黄疸的外科治疗
Arch Dis Child. 1965 Apr;40(210):158-61. doi: 10.1136/adc.40.210.158.
2
THORACIC DUCT-ESOPHAGUS ANASTOMOSIS FOR RELIEF OF CONGENITAL BILIARY ATRESIA.胸导管-食管吻合术治疗先天性胆道闭锁
Surg Forum. 1963;14:189-91.
3
[Atresia of the exterior biliary tract; hepatogastrostomy; lasting recovery after 12 months].[肝外胆道闭锁;肝胃吻合术;12个月后持久康复]
先天性胆道闭锁。
Nat Rev Dis Primers. 2024 Jul 11;10(1):47. doi: 10.1038/s41572-024-00533-x.
4
In Utero Extrahepatic Bile Duct Damage and Repair: Implications for Biliary Atresia.子宫内肝外胆管损伤与修复:对胆道闭锁的影响。
Pediatr Dev Pathol. 2024 Jul-Aug;27(4):291-310. doi: 10.1177/10935266241247479. Epub 2024 May 19.
5
Current and emerging adjuvant therapies in biliary atresia.胆道闭锁当前及新出现的辅助治疗方法。
Front Pediatr. 2022 Oct 14;10:1007813. doi: 10.3389/fped.2022.1007813. eCollection 2022.
6
Pediatric Cholestasis: Epidemiology, Genetics, Diagnosis, and Current Management.小儿胆汁淤积症:流行病学、遗传学、诊断及当前治疗方法
Clin Liver Dis (Hoboken). 2020 Apr 4;15(3):115-119. doi: 10.1002/cld.895. eCollection 2020 Mar.
7
Surgical modifications, additions, and alternatives to Kasai hepato-portoenterostomy to improve the outcome in biliary atresia.对Kasai肝门空肠吻合术进行手术改良、补充及替代方案以改善胆道闭锁的治疗效果。
Pediatr Surg Int. 2017 Dec;33(12):1275-1282. doi: 10.1007/s00383-017-4162-8. Epub 2017 Oct 4.
8
Morio Kasai: a remarkable impact beyond the Kasai procedure.増井道夫:超越葛西术的卓越影响力
J Pediatr Surg. 2012 May;47(5):1023-7. doi: 10.1016/j.jpedsurg.2012.01.065.
Zentralbl Chir. 1958 Mar 1;83(9):597-605.
4
Hepatic lymphatic drainage to the jejunum for congenital biliary atresia.先天性胆道闭锁的肝淋巴引流至空肠。
Am J Surg. 1966 Aug;112(2):188-94. doi: 10.1016/0002-9610(66)90008-0.
5
Intrahepatic biliary obstruction in congenital bile duct atresia.先天性胆管闭锁中的肝内胆管梗阻
Tohoku J Exp Med. 1969 Oct;99(2):129-49. doi: 10.1620/tjem.99.129.
6
Treatment of biliary atresia with special reference to hepatic porto-enterostomy and its modifications.胆道闭锁的治疗,特别提及肝门肠吻合术及其改良术。
Prog Pediatr Surg. 1974;6:5-52.
7
Reoperation in patients with biliary atresia.胆道闭锁患者的再次手术
J Pediatr Surg. 1985 Jun;20(3):256-9. doi: 10.1016/s0022-3468(85)80116-0.
8
Progress in the treatment of biliary atresia.胆道闭锁的治疗进展
World J Surg. 1985 Apr;9(2):285-93. doi: 10.1007/BF01656322.