Original contributionCytokeratin subsets can reliably distinguish Barrett's esophagus from intestinal metaplasia of the stomach
References (32)
Barrett's Esophagus, dysplasia, and adenocarcinoma
Hum Pathol
(1994)- et al.
Columnar-lined lower esophagus: an acquired lesion with malignant predisposition
J Thorac Cardiovasc Surg
(1975) - et al.
Barrett's esophagus: Age, prevalence and extent of columnar epithelium
Gastroenterol
(1992) - et al.
The catalog of human cytokeratins: Patterns of expression in normal epithelia, tumors and cultured cells
Cell
(1982) - et al.
Prevalence and characteristics of Barrett's esophagus in patients with adenocarcinoma of the esophagus or esophagogastric junction
Hum Pathol
(1988) - et al.
Prevalence of metaplasia at the gastro-oesophageal junction
Lancet
(1994) - et al.
Barrett's syndrome: Case report with discussion about concepts of pathogenesis
Gastroenterol
(1960) - et al.
Structural changes in the gastric foveolar epithelium in Helicobacter pylori-positive gastritis revealed by keratin immunohistochemistry
Hum Pathol
(1997) - et al.
Rising incidence of adenocarcinoma of the esophagus and gastric cardia
J Am Med Assoc
(1991) - et al.
Dysplasia in short-segment Barrett's' esophagus: A prospective 3-year follow up
Am J Gastroenterol
(1997)
Barrett's' esophagus: A review of the pathologist's role in diagnosis and management
Pathol Ann
(1991)
Cytokeratins in the histological diagnosis of malignant tumors
Int J Biol Markers
(1994)
Immunohistochemical demonstration of keratin 7 in routinely fixed paraffin-embedded human tissues
J Pathol
(1991)
Cytokeratin 20 in human carcinomas: A new histodiagnostic marker detected by monoclonal antibodies
Am J Pathol
(1992)
Coordinate expression of cytokeratins 7 and 20 defines unique subsets of carcinomas
Appl Immunohistochem
(1995)
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Keratin intermediate filaments in the colon: guardians of epithelial homeostasis
2020, International Journal of Biochemistry and Cell BiologyCitation Excerpt :Of the different CRC types, well and moderately differentiated adenocarcinomas, mucinous adenocarcinoma and signet ring cell carcinoma most frequently exhibited a K7-negative and K20-positive phenotype (Bayrak et al., 2011; Yamagishi et al., 2013). The lack of K7 expression (Fig. 4) is no surprise, as K7 is not usually found in healthy intestinal epithelia and considered a marker of ductal differentiation (Ormsby et al., 1999). Nevertheless, focal K7 expression is sometimes found in normal colon mucosa, especially close to cancerous tissue (Gurzu and Jung, 2012).
Some observations on Barrett esophagus and associated dysplasia
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