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一例未分类的先天性胆管囊肿。

An unclassified congenital bile duct cyst.

作者信息

Dumitrascu T, Ionescu M

出版信息

Acta Chir Belg. 2014 Jan-Feb;114(1):82-3.

PMID:24720146
Abstract

Congenital bile duct cysts are rare in adulthood. The most frequently used classification was proposed by Todani in 1977. However, in rare cases, not all the bile duct cysts are suitable to this classification. Hereby, we describe the case of an unclassified and very rare form of congenital bile duct cyst--isolated cystic duct cyst. En-block resection of the cyst, along with gallbladder, is the treatment of choice. Although exceptional, cystic duct cysts should be included in Todani classification so that the surgeons to be aware for this variation.

摘要

先天性胆管囊肿在成人中较为罕见。最常用的分类方法是由户谷于1977年提出的。然而,在罕见情况下,并非所有胆管囊肿都适用于这种分类。在此,我们描述一例未分类且极为罕见的先天性胆管囊肿——孤立性胆囊管囊肿的病例。囊肿连同胆囊整块切除是首选治疗方法。尽管罕见,但胆囊管囊肿应纳入户谷分类,以便外科医生了解这种变异情况。

相似文献

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An unclassified congenital bile duct cyst.一例未分类的先天性胆管囊肿。
Acta Chir Belg. 2014 Jan-Feb;114(1):82-3.
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Type VI Choledochal Cyst and the Anomalous Pancreaticobiliary Junction: A Systematic Review.Ⅵ型胆总管囊肿与胰胆管合流异常:一项系统综述
J Indian Assoc Pediatr Surg. 2025 May-Jun;30(3):277-289. doi: 10.4103/jiaps.jiaps_204_24. Epub 2025 Mar 3.
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Cystic duct cyst in adults: a systematic review of the sixth entity.成人胆囊管囊状扩张:第六种实体的系统综述。
Surg Today. 2023 May;53(5):527-543. doi: 10.1007/s00595-022-02461-3. Epub 2022 Feb 6.