2005
DOI: 10.1016/j.anndiagpath.2004.12.002
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Intestinal and oncocytic variants of pancreatic intraepithelial neoplasia. A morphological and immunohistochemical study

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Cited by 20 publications
(14 citation statements)
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“…Although the expression of CK20 was typically negative in both BilIN and PanIN in this study (data not shown), BilIN is not infrequently associated with metaplastic change of intestinal type, while intestinal-type PanIN is generally not found [12, 13]. These observations may explain the focal MUC2 expression in BilIN rather than in PanIN.…”
Section: Resultsmentioning
confidence: 50%
“…Although the expression of CK20 was typically negative in both BilIN and PanIN in this study (data not shown), BilIN is not infrequently associated with metaplastic change of intestinal type, while intestinal-type PanIN is generally not found [12, 13]. These observations may explain the focal MUC2 expression in BilIN rather than in PanIN.…”
Section: Resultsmentioning
confidence: 50%
“…2 and Supplementary Figures 8–12) is observed in 50% of IOPN‐P and IOPN‐B cases, and this proportion is comparable to IPMN‐P and IPMN‐B. The invasive carcinomas derived from IOPN‐P and IOPN‐B in the majority of cases have a tubular appearance (small glands or cribriform structures in desmoplastic stroma), but invasive solid nests without prominent desmoplasia may also be noticed [17, 18, 51]. Invasive compartments may retain or lose oncocytic features.…”
Section: Resultsmentioning
confidence: 99%
“…Ki‐67 proliferative index in IOPN‐P ranges from 5 to 30% [17, 51] and from 10% to 25% in IOPN‐B [18, 40, 42]. Proliferative activity of invasive carcinomas derived from IOPN was not specifically described.…”
Section: Resultsmentioning
confidence: 99%
“…In most instances, tumours with oncocytic features are well-defined entities, such as mucinous exocrine pancreatic tumours [3], pancreatic intraepithelial neoplasia [1], intraductal papillary neoplasms [20,31], thus, not representing difficulties in their differential diagnosis. However, oncocytic carcinomas, lacking neuroendocrine markers of differentiation or neurosecretory granules by electron microscopy, with predominant solid growth patterns and tumour cells with abundant eosinophilic cytoplasm have been observed and may represent a diagnostic problem [4,19,32,38,42].…”
Section: Discussionmentioning
confidence: 99%
“…In fact, cases of oncocytic tumours of the pancreas lacking neuroendocrine marker expression have been described [4,19,32,38,42]. Moreover, oncocytic changes have been described in mucinous exocrine pancreatic tumours [3], in pancreatic intraepithelial neoplasia [1] and in intraductal papillary neoplasms [20,31]. In addition, when diagnosed as metastatic deposits in the liver, differential diagnosis with primary hepatocellular carcinoma or with metastases from oncocytic tumours from other sites should also be considered.…”
Section: Introductionmentioning
confidence: 97%