Baik HyungJoo, Park Yo-Han, Seo Sang Hyuk, An Min Sung, Kim Kwang Hee, Bae Ki Beom, Choi Chang Soo, Oh Sang Hoon, Choi Young Kil
Department of Surgery, Busan Paik Hospital, College of Medicine, Inje University, Busan, Korea.
Ann Hepatobiliary Pancreat Surg. 2016 Nov;20(4):201-203. doi: 10.14701/ahbps.2016.20.4.201. Epub 2016 Nov 30.
This case report presents an unusual case of cholangiocarcinoma arising nearly 35 years after cystoduodenostomy for choledochal cyst. The patient visited our hospital with dyspepsia and studies revealed bezoar within the choledochal cyst caused by bile and food reflux. The patient underwent pancreaticoduodenectomy and a biopsy revealed adenocarcinoma, stage IIB. After 19 months, the patient has no recurrence to date and has recovered well. This case shows that proper surgical management and meticulous, long-term follow-up is imperative for patients with congenital choledochal cyst.
本病例报告呈现了一例罕见的胆管癌病例,该病例发生于胆总管囊肿行囊肿十二指肠吻合术后近35年。患者因消化不良前来我院就诊,检查发现胆总管囊肿内有由胆汁和食物反流导致的胃石。患者接受了胰十二指肠切除术,活检显示为腺癌,IIB期。19个月后,患者至今无复发,恢复良好。该病例表明,对于先天性胆总管囊肿患者,恰当的手术治疗及细致、长期的随访至关重要。