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The Rare Malignancy of the Hepatobiliary System: Ampullary Carcinoid Tumor
Author(s) -
Mustafa Özsoy,
Yücel Özsoy,
Aras Emre Canda,
Olcay Ak Nalbant,
Fatih Haskaraca
Publication year - 2011
Publication title -
case reports in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.2
H-Index - 20
eISSN - 1687-9627
pISSN - 1687-9635
DOI - 10.1155/2011/173036
Subject(s) - medicine , major duodenal papilla , malignancy , pancreaticoduodenectomy , duodenum , pathology , pathological , ampulla of vater , ampulla , carcinoid tumors , papillary tumor , radiology , gastroenterology , pancreas , carcinoma
. 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. Pylorus—preserving pancreaticoduodenectomy surgical procedure was applied. On pathological examination of the mass, a tumoral mass was detected in ampulla vateri localization, 1.5 × 1 × 0.8 cm 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.

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