The Rare Malignancy of the Hepatobiliary System: Ampullary Carcinoid Tumor

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 co...

Full description

Saved in:
Bibliographic Details
Main Authors: Mustafa Ozsoy, Yucel Ozsoy, Aras Emre Canda, Olcay Ak Nalbant, Fatih Haskaraca
Format: Article
Language:English
Published: Wiley 2011-01-01
Series:Case Reports in Medicine
Online Access:http://dx.doi.org/10.1155/2011/173036
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832551977659138048
author Mustafa Ozsoy
Yucel Ozsoy
Aras Emre Canda
Olcay Ak Nalbant
Fatih Haskaraca
author_facet Mustafa Ozsoy
Yucel Ozsoy
Aras Emre Canda
Olcay Ak Nalbant
Fatih Haskaraca
author_sort Mustafa Ozsoy
collection DOAJ
description 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. 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.
format Article
id doaj-art-cb93ed98344e4be09a4cbe11e3027ee4
institution Kabale University
issn 1687-9627
1687-9635
language English
publishDate 2011-01-01
publisher Wiley
record_format Article
series Case Reports in Medicine
spelling doaj-art-cb93ed98344e4be09a4cbe11e3027ee42025-02-03T06:00:05ZengWileyCase Reports in Medicine1687-96271687-96352011-01-01201110.1155/2011/173036173036The Rare Malignancy of the Hepatobiliary System: Ampullary Carcinoid TumorMustafa Ozsoy0Yucel Ozsoy1Aras Emre Canda2Olcay Ak Nalbant3Fatih Haskaraca4Department of General Surgery, Manisa State Hospital, 45000 Manisa, TurkeyDepartment of General Surgery, Manisa State Hospital, 45000 Manisa, TurkeyDepartment of General Surgery, Dokuz Eylul University School of Medicine, Izmir, TurkeyDepartment of Pathology, Manisa State Hospital, Manisa, TurkeyDepartment of General Surgery, Merkezefendi State Hospital, Manisa, TurkeyIntroduction. 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.http://dx.doi.org/10.1155/2011/173036
spellingShingle Mustafa Ozsoy
Yucel Ozsoy
Aras Emre Canda
Olcay Ak Nalbant
Fatih Haskaraca
The Rare Malignancy of the Hepatobiliary System: Ampullary Carcinoid Tumor
Case Reports in Medicine
title The Rare Malignancy of the Hepatobiliary System: Ampullary Carcinoid Tumor
title_full The Rare Malignancy of the Hepatobiliary System: Ampullary Carcinoid Tumor
title_fullStr The Rare Malignancy of the Hepatobiliary System: Ampullary Carcinoid Tumor
title_full_unstemmed The Rare Malignancy of the Hepatobiliary System: Ampullary Carcinoid Tumor
title_short The Rare Malignancy of the Hepatobiliary System: Ampullary Carcinoid Tumor
title_sort rare malignancy of the hepatobiliary system ampullary carcinoid tumor
url http://dx.doi.org/10.1155/2011/173036
work_keys_str_mv AT mustafaozsoy theraremalignancyofthehepatobiliarysystemampullarycarcinoidtumor
AT yucelozsoy theraremalignancyofthehepatobiliarysystemampullarycarcinoidtumor
AT arasemrecanda theraremalignancyofthehepatobiliarysystemampullarycarcinoidtumor
AT olcayaknalbant theraremalignancyofthehepatobiliarysystemampullarycarcinoidtumor
AT fatihhaskaraca theraremalignancyofthehepatobiliarysystemampullarycarcinoidtumor
AT mustafaozsoy raremalignancyofthehepatobiliarysystemampullarycarcinoidtumor
AT yucelozsoy raremalignancyofthehepatobiliarysystemampullarycarcinoidtumor
AT arasemrecanda raremalignancyofthehepatobiliarysystemampullarycarcinoidtumor
AT olcayaknalbant raremalignancyofthehepatobiliarysystemampullarycarcinoidtumor
AT fatihhaskaraca raremalignancyofthehepatobiliarysystemampullarycarcinoidtumor