Surgical and molecular pathology of pancreatic neoplasms

被引:89
作者
Hackeng, Wenzel M. [1 ]
Hruban, Ralph H. [2 ]
Offerhaus, G. Johan A. [1 ]
Brosens, Lodewijk A. A. [1 ]
机构
[1] Univ Med Ctr Utrecht, Dept Pathol, Heidelberglaan 100, NL-3584 CX Utrecht, Netherlands
[2] Johns Hopkins Univ, Sch Med, Dept Pathol, Sol Goldman Pancreat Canc Res Ctr, Baltimore, MD 21205 USA
关键词
Pancreas; Pancreatic cancer; Acinar cell carcinoma; Pancreatic neuroendocrine tumor; Solid-pseudopapillary neoplasm; Genetics; Histology; Methylation; microRNA; Sequencing; ACINAR-CELL-CARCINOMA; SOLID-PSEUDOPAPILLARY NEOPLASM; FAMILIAL ADENOMATOUS POLYPOSIS; DUCTAL ADENOCARCINOMA; NEUROENDOCRINE TUMORS; DNA METHYLATION; ALLELIC DELETIONS; GENE-EXPRESSION; POOR-PROGNOSIS; BETA-CATENIN;
D O I
10.1186/s13000-016-0497-z
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Background: Histologic characteristics have proven to be very useful for classifying different types of tumors of the pancreas. As a result, the major tumor types in the pancreas have long been classified based on their microscopic appearance. Main body: Recent advances in whole exome sequencing, gene expression profiling, and knowledge of tumorigenic pathways have deepened our understanding of the underlying biology of pancreatic neoplasia. These advances have not only confirmed the traditional histologic classification system, but also opened new doors to early diagnosis and targeted treatment. Conclusion: This review discusses the histopathology, genetic and epigenetic alterations and potential treatment targets of the five major malignant pancreatic tumors - pancreatic ductal adenocarcinoma, pancreatic neuroendocrine tumor, solid-pseudopapillary neoplasm, acinar cell carcinoma and pancreatoblastoma.
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页数:17
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