- 期刊
- OpenAccess
Choledochal Cyst in Siblings: Report of Two Cases in a Family
總膽管囊腫：家族性病例報告
並列摘要
Choledochal cysts are known to be one of the causes of childhood jaundice. Reported familial cases are extremely rare. Choledochal cyst in siblings was experienced at our hospital. They were observed to be rather well except for mild jaundice and abnormal stool color after admission. Biochemical studies revealed conjugated hyperbilirubinemia and elevated liver function. Abdominal sonogram disclosed cystic mass or fusiform dilatation of common bile duct (CBD). Intrahepatic duct (IHD) dilatation was noted in both patients. Operative findings revealed cystic dilatation of CBD in one patient and fusiform dilatation of CBD in another. They both received excision of cyst with Roux-en-Y hepaticojejunostomy and cholecystectomy. The postoperative course was uneventful.
延伸閱讀
- 蔡長晃（1982）。總胆管囊腫一個案分析與文獻回顧。中華放射線醫學雜誌，7(3)，210-219。https://www.airitilibrary.com/Article/Detail?DocID=10188940-198209-7-3-210-219-a
- Wu, H. S., Shen, K. L., Chen, T. K., Chang, T. M., & Hsu, T. M. (1990). 總膽管囊腫之外科治療. Journal of Medical Sciences, 10(5), 321-328. https://www.airitilibrary.com/Article/Detail?DocID=10114564-199010-201308010015-201308010015-321-328
- Cheng, S. J., Lee, C. H., & Chen, C. C. (1975). 先天性總膽管囊腫－不尋常臨床表徵之一例. Acta Paediatrica Sinica, 16(2), 79-83. https://www.airitilibrary.com/Article/Detail?DocID=00016578-197506-16-2-79-83-a
- Wu, Y. K., Chang, Y. J., Lee, Y. T. M., Chen, H. T., Huang, S. M., Lee, M. C., & Huang, Y. M. (2005). 發生於姙娠期間的總膽管囊腫－兩病例報告. 慈濟醫學雜誌, 17(4), 261-263. https://doi.org/10.6440/TZUCMJ.200507.0261
- Liu, C. L., Yang, K. C., & Lin, Y. N. (1987). 膽囊囊腺瘤：一例報告. 中華民國消化系醫學會雜誌, 4(2), 68-71. https://doi.org/10.6557/GJTa.198706_4(2).0004