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1.
Scand J Gastroenterol ; 47(2): 217-24, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22149906

ABSTRACT

OBJECTIVE: To investigate the negative predictive value of magnetic resonance cholangiopancreatography (MRCP) for common bile duct (CBD) stones and the prognosis of patients suspected to have choledocholithiasis in whom the MRCP was negative for CBD stones. METHODS: We enrolled the patients suspected to have choledocholithiasis in whom the MRCP was negative for the CBD stones between January 2008 and March 2011 and retrospectively analyzed the outcomes of 115 patients. RESULTS: Endoscopic retrograde cholangiopancreatography (ERCP) was performed in 27 patients (23%, group 1), and none had CBD stones. The negative predictive value of MRCP was 100%. During a median follow-up of 18.3 months, acute cholangitis with newly developed CBD stones occurred in two patients. Eighty-eight patients (77%, group 2) did not undergo ERCP and all recovered from acute cholangitis without CBD surgery. During a median follow-up of 18.7 months, acute cholangitis, acute cholecystitis, gallstone pancreatitis, and pancreatico-biliary cancers occurred in four (4.6%), three (3.5%), one (1.2%), and three (3.5%) patients, respectively. New CBD stones were found in only two patients among four patients with recurrent acute cholangitis. No patient had recurrent cholangitis caused by MRCP-missed CBD stones. The rates of recurrent cholangitis and cholangitis-free survival did not differ between groups 1 and 2. CONCLUSION: The negative predictive value of MRCP was very high. ERCP can be reserved for patients who are MRCP negative for choledocholithiasis, but close follow-up is needed because of recurrent cholangitis or pancreatico-biliary cancer.


Subject(s)
Cholangiopancreatography, Magnetic Resonance , Cholangitis/complications , Choledocholithiasis/complications , Choledocholithiasis/diagnosis , Acute Disease , Adult , Aged , Biliary Tract Neoplasms/complications , Cholangiopancreatography, Endoscopic Retrograde , Cholecystitis/complications , Choledocholithiasis/surgery , Disease-Free Survival , Female , Follow-Up Studies , Humans , Kaplan-Meier Estimate , Length of Stay , Male , Middle Aged , Pancreatic Neoplasms/complications , Pancreatitis/complications , Predictive Value of Tests , Prognosis , Recurrence , Retrospective Studies
2.
Korean J Gastroenterol ; 46(3): 189-95, 2005 Sep.
Article in Korean | MEDLINE | ID: mdl-16179838

ABSTRACT

BACKGROUND/AIMS: Barrett's esophagus is a premalignant lesion of the esophagus in which normal squamous epithelium is replaced by intestinalized columnar epithelium. In Korea, adenocarcinoma associated with Barrett's esophagus is rare compared with that of Western country. The purpose of this study was to investigate the immunohistochemical expression of p53 and Ki-67 in Barrett's esophagus which had predictive value for cancer risk in Korea. METHODS: Ninety five patients (43 male and 52 female, median age 44, range 21-75) who have been suspected to have Barrett's esophagus by endoscopic assessment were enrolled in this study. Alcian blue (pH 2.5) and high ion diamine stain for the evaluation of specialized intestinal metaplasia (SIM) and immunohistochemical stain for p53 and Ki-67 were done. RESULTS: 57.9% (55/95) of biopsies from the columnar lined esophagus showed SIM, but no dysplasia. 56.4% (31/55) of Barrett's esophagus showed sulfomucin positive colonic metaplasia. The p53 expression was observed in 10.9% (6/55) of the patients of Barrett's esophagus and all of them showed colonic metaplasia. Ki-67 labeling index showed no difference significantly. CONCLUSIONS: In Korea, 10.9% of Barrett's esophagus had p53 mutation and moreover all of them had colonic metaplasia. Consequently, we expect that these patients have high risk of developing dysplasia and adenocarcinoma and need careful follow-up.


Subject(s)
Barrett Esophagus/metabolism , Ki-67 Antigen/metabolism , Tumor Suppressor Protein p53/metabolism , Adenocarcinoma/etiology , Adenocarcinoma/genetics , Adult , Aged , Barrett Esophagus/complications , Esophageal Neoplasms/etiology , Esophageal Neoplasms/genetics , Female , Humans , Immunohistochemistry , Male , Middle Aged , Risk Factors
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