Clark G W, Smyrk T C, Burdiles P, Hoeft S F, Peters J H, Kiyabu M, Hinder R A, Bremner C G, DeMeester T R
Department of Surgery, University of Southern California School of Medicine, Los Angeles.
Arch Surg. 1994 Jun;129(6):609-14. doi: 10.1001/archsurg.1994.01420300051007.
To investigate the prevalence of Barrett's esophagus in patients with adenocarcinomas located at the gastroesophageal junction.
A case series of patients who underwent esophagogastrectomy for adenocarcinoma was retrospectively reviewed. Tumors were grouped by location as esophageal, cardiac, and subcardiac, and the prevalence of specialized intestinal metaplasia in the histological specimens was determined.
A university department of surgery that specializes in esophageal diseases.
One hundred patients with adenocarcinoma of the esophagus, cardia, or proximal stomach.
Cardiac adenocarcinomas were associated with Barrett's esophagus in 42% of the patients.
Specialized intestinal metaplasia was identified in the histological sections from the resected specimen in 42% (13/31) of cardiac adenocarcinomas and in 79% (38/48) of esophageal adenocarcinomas but in only 5% (1/21) of subcardiac adenocarcinomas. The preoperative endoscopic biopsy results concurred with the final diagnosis of Barrett's esophagus in 33 of the 38 esophageal tumors, six of the 13 cardiac tumors, and the one subcardiac tumor but failed to detect specialized intestinal metaplasia in 54% (7/13) of cardiac tumors. Cardiac tumors were associated with shorter lengths of Barrett's mucosa than esophageal tumors (2.7 +/- 1.8 cm vs 7.4 +/- 3.4 cm, P < .01). The Barrett's metaplasia was dysplastic in 36 of the 38 esophageal tumors, 10 of the 13 cardiac tumors, but not in the subcardiac tumor.
Adenocarcinomas located at the gastroesophageal junction were associated with Barrett's metaplasia in nearly one half of the patients. The length of the Barrett segment tends to be short and may be missed during endoscopy. The presence of high-grade dysplasia within Barrett's mucosa supports a barrett's origin for half of the adenocarcinomas arising at this location.
研究胃食管交界腺癌患者中巴雷特食管的患病率。
对因腺癌接受食管胃切除术的患者进行回顾性病例系列研究。肿瘤按位置分为食管型、贲门型和贲门下型,并确定组织学标本中特殊肠化生的患病率。
一所专门治疗食管疾病的大学外科科室。
100例食管、贲门或近端胃腺癌患者。
42%的患者贲门腺癌与巴雷特食管相关。
在切除标本的组织学切片中,42%(13/31)的贲门腺癌、79%(38/48)的食管腺癌发现有特殊肠化生,而贲门下腺癌仅5%(1/21)有特殊肠化生。术前内镜活检结果与38例食管肿瘤中的33例、13例贲门肿瘤中的6例以及1例贲门下肿瘤的巴雷特食管最终诊断一致,但在54%(7/13)的贲门肿瘤中未能检测到特殊肠化生。贲门肿瘤的巴雷特黏膜长度比食管肿瘤短(2.7±1.8 cm对7.4±3.4 cm,P<0.01)。38例食管肿瘤中的36例、13例贲门肿瘤中的10例巴雷特化生有发育异常,但贲门下肿瘤无发育异常。
近一半胃食管交界腺癌患者与巴雷特化生相关。巴雷特段长度往往较短,在内镜检查时可能漏诊。巴雷特黏膜内高级别发育异常的存在支持了该部位发生的腺癌中有一半起源于巴雷特食管。