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Short-segment Barrett's esophagus and cardia intestinal metaplasia: A comparative analysis.短节段 Barrett 食管及贲门肠化生:对比分析。
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Differences in genetic instability and cellular phenotype among Barrett's, cardiac, and gastric intestinal metaplasia in a Japanese population with Helicobacter pylori.在日本幽门螺杆菌感染人群中,Barrett食管、贲门及胃小肠化生之间的基因不稳定性和细胞表型差异。
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本文引用的文献

1
Distinction between intestinal metaplasia in the cardia and in Barrett's esophagus: the role of histology and immunohistochemistry.贲门肠化生与巴雷特食管肠化生的鉴别:组织学和免疫组织化学的作用
Hum Pathol. 2004 Mar;35(3):371-6. doi: 10.1016/j.humpath.2003.09.011.
2
Barrett's esophagus: histopathologic definitions and diagnostic criteria.巴雷特食管:组织病理学定义与诊断标准
World J Surg. 2004 Feb;28(2):148-54. doi: 10.1007/s00268-003-7050-4. Epub 2004 Jan 20.
3
The utility of cytokeratins 7 and 20 (CK7/20) immunohistochemistry in the distinction of short-segment Barrett esophagus from gastric intestinal metaplasia: Is it reliable?细胞角蛋白7和20(CK7/20)免疫组化在区分短节段巴雷特食管与胃肠化生中的应用:是否可靠?
BMC Clin Pathol. 2003 Dec 2;3(1):5. doi: 10.1186/1472-6890-3-5.
4
Phenotypic differences between esophageal and gastric intestinal metaplasia.食管化生和胃化生之间的表型差异。
Mod Pathol. 2004 Jan;17(1):62-74. doi: 10.1038/sj.modpathol.3800016.
5
Primary adenocarcinomas of lower esophagus, esophagogastric junction and gastric cardia: in special reference to China.食管下段、食管胃交界部和贲门原发性腺癌:特别提及中国情况
World J Gastroenterol. 2003 Jun;9(6):1156-64. doi: 10.3748/wjg.v9.i6.1156.
6
Intestinal metaplasia at the gastroesophageal junction: Barrett's, bacteria, and biomarkers.胃食管交界处的肠化生:巴雷特食管、细菌与生物标志物
Am J Gastroenterol. 2003 Apr;98(4):759-62. doi: 10.1111/j.1572-0241.2003.07393.x.
7
Cytokeratin and DAS-1 immunostaining reveal similarities among cardiac mucosa, CIM, and Barrett's esophagus.细胞角蛋白和DAS-1免疫染色显示心脏黏膜、腐蚀性食管炎和巴雷特食管之间存在相似之处。
Am J Gastroenterol. 2002 Oct;97(10):2514-23. doi: 10.1111/j.1572-0241.2002.06033.x.
8
Etiology of intestinal metaplasia at the gastroesophageal junction.胃食管交界处肠化生的病因
Surg Endosc. 2003 Jan;17(1):43-8. doi: 10.1007/s00464-002-8944-1. Epub 2002 Oct 8.
9
Specialized intestinal metaplasia and carditis at the gastroesophageal junction in Chinese patients undergoing endoscopy.接受内镜检查的中国患者胃食管交界处的特殊肠化生和贲门炎。
Am J Gastroenterol. 2002 Aug;97(8):1924-9. doi: 10.1111/j.1572-0241.2002.05901.x.
10
Small adenocarcinomas of the esophagogastric junction: association with intestinal metaplasia and dysplasia.食管胃交界部小腺癌:与肠化生及发育异常的关联
Am J Gastroenterol. 2002 Jun;97(6):1375-80. doi: 10.1111/j.1572-0241.2002.05669.x.

短节段巴雷特食管与贲门肠化生的鉴别

Distinction between short-segment Barrett's esophageal and cardiac intestinal metaplasia.

作者信息

Liu Gui-Sheng, Gong Jun, Cheng Peng, Zhang Jun, Chang Ying, Qiang Lei

机构信息

Department of Gastroenterology, Second Hospital of Xi'an Jiaotong University, Xi'an 710004, Shaanxi Province, China.

出版信息

World J Gastroenterol. 2005 Oct 28;11(40):6360-5. doi: 10.3748/wjg.v11.i40.6360.

DOI:10.3748/wjg.v11.i40.6360
PMID:16419166
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4320341/
Abstract

AIM

To investigate the roles of mucin histochemistry, cytokeratin 7/20 (CK7/20) immunoreactivity, clinical characteristics and endoscopy to distinguish short-segment Barrett's esophageal (SSBE) from cardiac intestinal metaplasia (CIM).

METHODS

High iron diamine/Alcian blue (HID/AB) mucin-histochemical staining and immunohistochemical staining were used to classify intestinal metaplasia (IM) and to determine CK7/20 immunoreactivity pattern in SSBE and CIM, respectively, and these results were compared with endoscopical diagnosis and the positive rate of gastroesophageal reflux disease (GERD) symptoms and H pylori infection. Long-segment Barrett's esophageal and IM of gastric antrum were designed as control.

RESULTS

The prevalence of type III IM was significantly higher in SSBE than in CIM (63.33% vs 23.08%, P< 0.005). The CK7/20 immunoreactivity in SSBE showed mainly Barrett's pattern (76.66%), and the GERD symptoms in most cases which showed Barrett's pattern were positive, whereas H pylori infection was negative. However, the CK7/20 immunoreactivity in CIM was gastric pattern preponderantly (61.54%), but there were 23.08% cases that showed Barrett's pattern. H pylori infection in all cases which showed gastric pattern was significantly higher than those which showed Barrett's pattern (63.83% vs 19.30%, P< 0.005), whereas the GERD symptoms in gastric pattern were significantly lower than that in Barrett's pattern (21.28% vs 85.96%, P< 0.005).

CONCLUSION

Distinction of SSBE from CIM should not be based on a single method; however, the combination of clinical characteristics, histology, mucin histochemistry, CK7/20 immunoreactivity, and endoscopic biopsy should be applied. Type III IM, presence of GERD symptoms, and Barrett's CK7/20 immunoreactivity pattern may support the diagnosis of SSBE, whereas non-type III IM, positive H pylori infection, and gastric CK7/20 immunoreactivity pattern may imply CIM.

摘要

目的

探讨黏蛋白组织化学、细胞角蛋白7/20(CK7/20)免疫反应性、临床特征及内镜检查在区分短节段Barrett食管(SSBE)和贲门肠化生(CIM)中的作用。

方法

采用高铁二胺/阿尔辛蓝(HID/AB)黏蛋白组织化学染色和免疫组织化学染色分别对肠化生(IM)进行分类,并确定SSBE和CIM中CK7/20的免疫反应性模式,将这些结果与内镜诊断以及胃食管反流病(GERD)症状和幽门螺杆菌感染的阳性率进行比较。以长节段Barrett食管和胃窦IM作为对照。

结果

SSBE中III型IM的患病率显著高于CIM(63.33%对23.08%,P<0.005)。SSBE中CK7/20免疫反应性主要表现为Barrett模式(76.66%),大多数表现为Barrett模式的病例中GERD症状呈阳性,而幽门螺杆菌感染呈阴性。然而,CIM中CK7/20免疫反应性主要为胃型(61.54%),但有23.08%的病例表现为Barrett模式。所有表现为胃型的病例中幽门螺杆菌感染显著高于表现为Barrett模式的病例(63.83%对19.30%,P<0.005),而胃型中的GERD症状显著低于Barrett模式(21.28%对85.96%,P<0.005)。

结论

区分SSBE和CIM不应仅基于单一方法;然而,应综合应用临床特征、组织学、黏蛋白组织化学、CK7/20免疫反应性和内镜活检。III型IM、GERD症状的存在以及Barrett型CK7/20免疫反应性模式可能支持SSBE的诊断,而非III型IM、幽门螺杆菌感染阳性和胃型CK7/20免疫反应性模式可能提示CIM。