Carcinoma arising in a congenitally dilated biliary tract. Report of a case and review of the literature.
Carcinoma arising in a congenitally dilated biliary tract. Report of a case and review of the literature.
复制标题
先天性扩张的胆道产生的癌。
DOI：
10.5555/uri:pii:0016508578907084
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发表时间：
1978
期刊：
影响因子：
29.4
通讯作者：
S. Maetani
中科院分区：
文献类型：
--
作者：
Y. Kagawa;S. Kashihara;S. Kuramoto;S. Maetani
据报道，一例先天性扩张的胆道发生癌的病例。在世界文献中发现并分析了 47 例先天性胆道扩张与癌症相关的病例。发现癌症与先天性胆管扩张的关联性比以前认识的要高。癌可能发生在肝外或肝内的任何囊性部分。如果技术上安全可行，建议对胆总管囊肿进行一期切除，以防止未切除囊肿日后恶变的风险。
A case of carcinoma arising in a congenitally dilated biliary tract is reported. Forty-seven cases in which congenital dilatation of the biliary tract was associated with carcinoma were found in the world literature and analyzed. The association of carcinoma with congenital biliary ductal dilatation was found to be higher than previously recognized. Carcinoma may arise in any cystic portion, extrahepatic or intrahepatic. If technically safe and feasible, primary excision of the choledochal cyst is advisable, to prevent the risk of later malignant change in the unexcised cyst.