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胆总管囊肿——三例报告及文献复习

Choledochal cysts--report of three cases and review.

作者信息

Waldron R, Drumm J, McCarthy C F, Murphy B

出版信息

Postgrad Med J. 1984 Jun;60(704):397-9. doi: 10.1136/pgmj.60.704.397.

Abstract

Three cases of choledochal cyst are presented, with a review of previous publications. We re-emphasize the diagnostic dilemma involved and discuss current surgical management. A new complication is illustrated and an association with polycystic kidneys is reported. Choledochal cysts are uncommon, but correct management ensures a symptom-free future for the patient. Recent reports support cyst excision if technically feasible.

摘要

本文报告三例胆总管囊肿病例,并回顾以往文献。我们再次强调其中涉及的诊断困境,并讨论当前的手术治疗方法。文中阐述了一种新的并发症,并报告了与多囊肾的关联。胆总管囊肿并不常见,但正确的治疗可确保患者未来无病痛。近期报告支持在技术可行的情况下进行囊肿切除术。

相似文献

1
Choledochal cysts--report of three cases and review.胆总管囊肿——三例报告及文献复习
Postgrad Med J. 1984 Jun;60(704):397-9. doi: 10.1136/pgmj.60.704.397.
2
Choledochal cyst: diagnosis in neonates.胆总管囊肿:新生儿期的诊断
South Med J. 1988 Dec;81(12):1566-8. doi: 10.1097/00007611-198812000-00024.
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Choledochal cyst: review and report of four patients.
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Ultrasonographic appearance of multiseptate gallbladder: report a case with coexisting choledochal cyst.
J Clin Ultrasound. 1985 Oct;13(8):570-3. doi: 10.1002/1097-0096(199010)13:8<570::aid-jcu1870130810>3.0.co;2-h.

本文引用的文献

2
Congenital cystic dilatation of the common bile duct.先天性胆总管囊肿
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J Pediatr Surg. 1971 Apr;6(2):112-20. doi: 10.1016/0022-3468(71)90303-4.
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Congenital cystic disease of the liver and biliary system.先天性肝和胆道系统囊性疾病
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