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Endoscopic features of esophageal adenocarcinoma derived from short-segment versus long-segment Barrett's esophagus

机译:食管腺癌的内窥镜特征来自短段与长段Barrett的食道

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Background and Aim The study aims to clarify the endoscopic features and clinicopathological differences in superficial Barret's esophageal adenocarcinoma (s-BEA) derived from short-segment Barrett's esophagus (SSBE) and long-segment Barrett's esophagus (LSBE). Methods We reviewed data of 130 patients (141 lesions) with pathologically confirmed s-BEA (SSBE: 95 patients and 95 lesions; LSBE: 35 patients and 46 lesions). We analyzed endoscopic and clinicopathological features of s-BEA in patients with SSBE and LSBE. Results The distribution of lesions according to macroscopic findings were as follows (s-BEA in SSBE vs LSBE): flat type (0-IIb), 3.2% (3/95) vs 32.6% (15/46) (P < 0.001); accompanied type 0-IIb, 2.1% (2/95) vs 21.7% (10/46) (P < 0.001); and complex type (0-I + IIb, 0-IIa + IIc, etc.), 30.5% (29/95) vs 50.0% (23/46) (P = 0.025). Complex-type s-BEAs had high incidences of T1b invasions and poorly differentiated components (simple type: 22.5% [20/89] and 18.0% [16/89]; complex type: 59.6% [31/52] and 44.2% [23/52], P P = 0.002, respectively). In SSBE, 72.6% (69/95) of lesions were located at the right anterior wall (P = 0.01). All flat-type or depressed-type lesions derived from SSBE were identified as reddish areas, whereas only 65.2% (15/23) from LSBE were identified as reddish areas (P < 0.001). Conclusions In LSBE, flat-type, accompanied-type 0-IIb, and complex-type lesions were significantly more prevalent. Furthermore, complex-type s-BEAs tended to have T1b invasions and poorly differentiated components. S-BEAs in LSBE should be more carefully evaluated on endoscopic appearance including flat-type and complex-type lesions than in SSBE.
机译:背景技术该研究旨在阐明来自短段巴雷特食道(SSBE)和长段Barrett的食道(LSBE)的浅表毛刺食管腺癌(S-BEA)的内窥镜特征和临床病理差异。方法审查了130名患者(141例病变)的数据,病于病理证实的S-BEA(SSBE:95名患者和95例病变; LSBE:35名患者和46个病变)。我们分析了S-BAB的内窥镜和临床病理特征,在SSBE和LSBE患者中。结果根据宏观发现的病变分布如下(S-BEA在SSBE VS LSBE中):平型(0-IIB),3.2%(3/95)与32.6%(15/46)(P <0.001) ;伴随0-IIB,2.1%(2/95)与21.7%(10/46)(p <0.001);复杂类型(0-I + IIB,0-IIA + IIC等),30.5%(29/95)与50.0%(23/46)(p = 0.025)。复杂型S-BEA具有高血小胺T1B入侵和分化差的成分(简单类型:22.5%[20/89]和18.0%[16/89];复杂类型:59.6%[31/52]和44.2%[ 23/52],PP = 0.002分别)。在SSBE中,72.6%(69/95)的病变位于右侧壁(P = 0.01)。衍生自SSBE的所有扁平型或抑郁型病变被识别为红地区,而LSBE只有65.2%(15/23)被鉴定为Reddish区域(P <0.001)。结论LSBE,扁平型,伴奏型0-IIB和复杂型病变显着普遍。此外,复杂型S-BEA倾向于具有T1B侵入和分化不良的组分。 LSBE中的S-BEA应更仔细地在内窥镜外观上进行,包括扁平型和复杂型病变而不是SSBE。

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