Abstract
Introduction. Carcinoid tumors are low-grade tumors originating from endoderm and mostly involving the gastrointestinal system. However; they may be seen in any site within the gastrointestinal system. Case Presentation. A 69-year-old female patient. The results of blood tests were observed to be consistent with obstructive jaundice. A mass appearance was not encountered on tomographic examination. Papilla that was tumor-like macroscopically was seen in the second part of the duodenum in diagnostic endoscopy. Pyloruspreserving pancreaticoduodenectomy surgical procedure was applied. On pathological examination of the mass, a tumoral mass was detected in ampulla vateri localization, 1.5 × 1 × 0.8cm in size, which, in immunohistochemical staining, was evaluated as a neuroendocrine tumor. Also, Metastasis was observed. Conclusion. The rarest type of carcinoid tumor is ampullary located carcinoid tumor, and tumor size is not a reliable indicator for tumor aggressivity in ampullary carcinoid tumors. Copyright © 2011 Mustafa Ozsoy et al.
Cite
CITATION STYLE
Ozsoy, M., Ozsoy, Y., Canda, A. E., Nalbant, O. A., & Haskaraca, F. (2011). The rare malignancy of the hepatobiliary system: Ampullary carcinoid tumor. Case Reports in Medicine, 2011. https://doi.org/10.1155/2011/173036
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.