Ushijima Tomoyuki, Okabe Yoshinobu, Ishida Yusuke, Sugiyama Gen, Sasaki Yu, Kuraoka Kei, Yasumoto Makiko, Taira Tomoki, Naito Yoshiki, Nakayama Masamichi, Tsuruta Osamu, Sata Michio
Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka, Japan.
Department of Diagnostic Pathology, Kurume University School of Medicine, Kurume, Fukuoka, Japan.
Mol Clin Oncol. 2014 Jul;2(4):599-603. doi: 10.3892/mco.2014.277. Epub 2014 Apr 14.
With the advances in the multidisciplinary treatment of pancreatic cancer (PC) over the last few years, it is crucial to obtain a histopathological diagnosis prior to treatment. Histopathological diagnosis for unresectable PC is currently performed with endoscopic retrograde cholangiopancreatography (ERCP) in combination with endoscopic ultrasound-guided fine-needle aspiration (EUS-FNA). We retrospectively assessed the results of these two methods and investigated diagnostic performance according to the location of the lesion and the complications. This study was conducted on a series of 263 consecutive cases of unresectable PC diagnosed with endoscopic cytology. Up to 2006, ERCP-guided cytology (group A) was performed as the first choice for the diagnosis of PC. EUS-FNA was introduced in 2007 and became the first choice thereafter (group B), except in cases with obstructive jaundice, in which ERCP-guided cytology during endoscopic biliary stenting (EBS) remains the first choice. There were statistically significant differences in the overall cancer-positive rate between groups A and B (60.4 vs. 75.3%, P=0.01). The cancer-positive rate in the pancreatic body and tail was significantly higher in group B (59.5 vs. 83.3%, P=0.005), whereas there were no significant differences regarding cancer of the pancreatic head. The complication rate was 4.95% in group A and 3.09% in group B (P=0.448). The endoscopic cytology cancer-positive rate in unresectable PC cases was increased as a result of the introduction of EUS-FNA. In conclusion, we recommend performing EUS-FNA in combination with ERCP-guided cytology in cases with a lesion in the pancreatic head that requires EBS.
随着过去几年胰腺癌(PC)多学科治疗的进展,在治疗前获得组织病理学诊断至关重要。目前,不可切除PC的组织病理学诊断是通过内镜逆行胰胆管造影(ERCP)联合内镜超声引导下细针穿刺抽吸(EUS-FNA)来进行的。我们回顾性评估了这两种方法的结果,并根据病变位置和并发症调查了诊断性能。本研究对一系列263例经内镜细胞学诊断为不可切除PC的连续病例进行。截至2006年,ERCP引导下细胞学检查(A组)作为PC诊断的首选方法。2007年引入了EUS-FNA,此后成为首选方法(B组),但梗阻性黄疸病例除外,此类病例在内镜下胆道支架置入术(EBS)期间ERCP引导下细胞学检查仍是首选。A组和B组的总体癌症阳性率存在统计学显著差异(60.4%对75.3%,P=0.01)。B组胰体和胰尾的癌症阳性率显著更高(59.5%对83.3%,P=0.005),而胰头癌方面无显著差异。A组的并发症发生率为4.95%,B组为3.09%(P=0.448)。由于引入了EUS-FNA,不可切除PC病例的内镜细胞学癌症阳性率有所提高。总之,对于需要EBS且胰头有病变的病例,我们建议将EUS-FNA与ERCP引导下细胞学检查联合进行。