| Literature DB >> 31545536 |
Atsushi Nakayama1, Motohiko Kato1,2, Yusaku Takatori1, Masayuki Shimoda3, Mari Mizutani1,2, Koshiro Tsutsumi1, Yoshiyuki Kiguchi1, Teppei Akimoto1, Motoki Sasaki1, Makoto Mutaguchi4, Kaoru Takabayashi4, Tadateru Maehata1, Yasutoshi Ochiai1, Takanori Kanai2, Naohisa Yahagi1.
Abstract
There are no reports on detailed endoscopic diagnosis of superficial non-ampullary duodenal epithelial tumors (SNADET) except for relatively small case series. Herein, we conducted a prospective observational study to investigate the relationship between endoscopic findings and histopathological diagnosis of SNADET. A total of 163 SNADET diagnosed using magnified endoscopic examination with image-enhanced endoscopy (IEE-ME) were prospectively registered in this study. We investigated location, size, macroscopic type, color, and IEE-ME findings including surface structure (closed- or open-loop) and presence of white opaque substance (WOS) in SNADET. We analyzed association between these findings and histopathological diagnosis of SNADET based on the Vienna classification (VCL) using logistic regression analysis. In univariate analysis, lesion size, superficial structure, and WOS deposition showed statistical significance, and the oral side of the lesion location showed statistical tendency for association with VCL C4/5. In multivariate analysis, lesion size (odds ratio [OR], 2.92; 95% CI, 1.94-4.39; P < 0.05) and negative WOS (OR, 5.59; 95% CI, 1.72-18.1; P < 0.05) were significantly associated with VCL C4/5 lesions. Superficial structures with a closed-loop pattern on the surface showed statistical tendency for predicting VCL C4/5 lesions (OR, 2.15; 95% CI, 0.86-5.37; P = 0.10). Based on these findings, we concluded that negative WOS by IEE-ME and lesion size were independent predictors of VCL C4/5 SNADET. These factors may help us to understand of pathophysiology of SNADET and to select appropriate therapeutic strategies.Entities:
Keywords: adenoma; carcinoma; diagnosis; duodenal neoplasm; endoscopy
Mesh:
Year: 2019 PMID: 31545536 DOI: 10.1111/den.13538
Source DB: PubMed Journal: Dig Endosc ISSN: 0915-5635 Impact factor: 7.559