TY - JOUR
T1 - Elevated bile amylase level without pancreaticobiliary maljunction is a risk factor for gallbladder carcinoma
AU - Fujimoto, Takaaki
AU - Takao, Ohtsuka
AU - Nakashima, Yohei
AU - Gotoh, Yoshitaka
AU - Date, Kenjiro
AU - Mori, Yasuhisa
AU - Sadakari, Yoshihiko
AU - Takahata, Shunichi
AU - Oda, Yoshinao
AU - Nakamura, Masafumi
N1 - Funding Information:
The authors thank Dr Junji Kishimoto of the Center for Clinical and Translational Research at Kyushu University Hospital (Fukuoka, Japan) for his instruction in the statistical methods used in this study. The Japan Society for the Promotion of Science (JSPS: KAKENHI, grant number 15K10186) supported this study.
Publisher Copyright:
© 2017 Japanese Society of Hepato-Biliary-Pancreatic Surgery
PY - 2017/2/1
Y1 - 2017/2/1
N2 - Background: Elevated bile amylase level in patients with pancreaticobiliary maljunction (PBM) or high confluence of pancreaticobiliary ducts (HCPBD) is well known as a risk factor for gallbladder carcinoma (GBC) development. However, the effects of occult pancreaticobiliary reflux (OPR), a condition characterized by high bile amylase level in the presence of an anatomically normal pancreaticobiliary junction, on GBC development remain unclear. The aim of this study was to assess the relationship between OPR and GBC. Methods: Clinicopathological data of 52 patients who were preoperatively diagnosed with gallbladder (GB) tumor (22 malignant, 30 benign) were retrospectively reviewed. All of the patients underwent preoperative endoscopic retrograde cholangiopancreatography to evaluate pancreaticobiliary junction morphology and bile amylase level. The relationship between the histological diagnosis of GB lesions, and pancreaticobiliary junction morphology and bile amylase level were investigated. Results: Pancreaticobiliary maljunction, HCPBD, and normal pancreaticobiliary junction (NPJ) were identified in 12, nine, and 31 patients, respectively. The rates of GBC in patients with PBM, HCPBD, and NPJ were 58% (7/12), 67% (6/9), and 29% (9/31), respectively. Of the 31 patients with NPJ, 22 had OPR and nine of these had GBC. None of the patients with NPJ and normal bile amylase level had GBC. Additionally, among patients with NPJ, bile amylase level was significantly higher in patients with GBC than in patients with benign tumors. Conclusions: Occult pancreaticobiliary reflux, like PBM and HCPBD, is a risk factor for GBC development.
AB - Background: Elevated bile amylase level in patients with pancreaticobiliary maljunction (PBM) or high confluence of pancreaticobiliary ducts (HCPBD) is well known as a risk factor for gallbladder carcinoma (GBC) development. However, the effects of occult pancreaticobiliary reflux (OPR), a condition characterized by high bile amylase level in the presence of an anatomically normal pancreaticobiliary junction, on GBC development remain unclear. The aim of this study was to assess the relationship between OPR and GBC. Methods: Clinicopathological data of 52 patients who were preoperatively diagnosed with gallbladder (GB) tumor (22 malignant, 30 benign) were retrospectively reviewed. All of the patients underwent preoperative endoscopic retrograde cholangiopancreatography to evaluate pancreaticobiliary junction morphology and bile amylase level. The relationship between the histological diagnosis of GB lesions, and pancreaticobiliary junction morphology and bile amylase level were investigated. Results: Pancreaticobiliary maljunction, HCPBD, and normal pancreaticobiliary junction (NPJ) were identified in 12, nine, and 31 patients, respectively. The rates of GBC in patients with PBM, HCPBD, and NPJ were 58% (7/12), 67% (6/9), and 29% (9/31), respectively. Of the 31 patients with NPJ, 22 had OPR and nine of these had GBC. None of the patients with NPJ and normal bile amylase level had GBC. Additionally, among patients with NPJ, bile amylase level was significantly higher in patients with GBC than in patients with benign tumors. Conclusions: Occult pancreaticobiliary reflux, like PBM and HCPBD, is a risk factor for GBC development.
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U2 - 10.1002/jhbp.421
DO - 10.1002/jhbp.421
M3 - Article
C2 - 28002646
AN - SCOPUS:85013026906
SN - 1868-6974
VL - 24
SP - 103
EP - 108
JO - Journal of Hepato-Biliary-Pancreatic Sciences
JF - Journal of Hepato-Biliary-Pancreatic Sciences
IS - 2
ER -