Literature DB >> 11075851

Carcinoid tumors of the extrahepatic bile ducts: a study of seven cases.

A Maitra1, J E Krueger, M Tascilar, G J Offerhaus, A Angeles-Angeles, D S Klimstra, R H Hruban, J Albores-Saavedra.   

Abstract

The authors report seven patients with carcinoid tumors of the extrahepatic bile ducts (EHBDs). All patients were women, with an average age at diagnosis of 49.8 years (range, 37-67 yrs). The most common presenting symptom was painless jaundice with or without pruritus. Although one patient had peptic ulcer disease before the onset of obstructive jaundice, none had systemic endocrine manifestations. These neoplasms were most often located in the common bile duct. Grossly, the carcinoid tumors were usually nodular and poorly demarcated, and ranged from 1.1 to 2.7 cm in size. Only one of the neoplasms was polypoid. Microscopically, the tumors had a trabecular or nesting pattern with occasional tubule formation, and were composed of relatively small cells with granular chromatin. All of the neoplasms expressed chromogranin and two expressed synaptophysin. Three expressed serotonin and two of the three were also immunoreactive for pancreatic polypeptide or somatostatin. Two tumors were focally positive for gastrin and one of these two tumors was also positive for serotonin and pancreatic polypeptide. All seven carcinoid tumors showed no immunoreactivity for p53, and assays for p53 loss of heterozygosity analysis were negative in two, suggesting that p53 mutations do not play a role in the pathogenesis of EHBD carcinoids. A mutation in codon 12 of K-ras was found in one carcinoid tumor whereas two of two showed immunoreactivity for Dpc4 protein. In view of the small number of carcinoids studied, the importance of these findings in the pathogenesis of these tumors is unclear. Ultrastructural examination of three of the tumors revealed numerous membrane-bound, round neurosecretory granules. Clinically, these lesions had an indolent course. Even in the presence of lymph node metastases (noted in two patients), all of the patients remained disease free 2 to 11 years (average follow up, 6.6 yrs) after segmental resection or pancreaticoduodenectomy (Whipple's procedure). Because carcinoid tumors of the EHBD are of low malignant potential, they should be separated from the more common adenocarcinomas in this location.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 11075851     DOI: 10.1097/00000478-200011000-00005

Source DB:  PubMed          Journal:  Am J Surg Pathol        ISSN: 0147-5185            Impact factor:   6.394


  17 in total

Review 1.  Well-Differentiated Neuroendocrine Tumour of the Extrahepatic Bile Duct: a Case Report with Review of Literature.

Authors:  Mohamed Safwan; Mukul Vij; Sanjay Govil; Mohamed Rela
Journal:  J Gastrointest Cancer       Date:  2016-03

Review 2.  An analysis of rare carcinoid tumors: clarifying these clinical conundrums.

Authors:  Irvin M Modlin; Michael D Shapiro; Mark Kidd
Journal:  World J Surg       Date:  2005-01       Impact factor: 3.352

Review 3.  Neuroendocrine tumors of extrahepatic biliary tract.

Authors:  Nickos Michalopoulos; Theodossis S Papavramidis; Georgia Karayannopoulou; Ioannis Pliakos; Spiros T Papavramidis; Ioannis Kanellos
Journal:  Pathol Oncol Res       Date:  2014-06-11       Impact factor: 3.201

4.  Carcinoid tumors of the extrahepatic biliary tract: report of four cases.

Authors:  Jae Hoon Lee; Kyeong Geun Lee; Young Ha Oh; Seung Sam Paik; Hwon Kyum Park; Kwang Soo Lee
Journal:  Surg Today       Date:  2011-03-02       Impact factor: 2.549

5.  Carcinoid tumor of the extrahepatic bile duct: report of a case.

Authors:  Takeo Yasuda; Gen Imai; Masako Takemoto; Mitsuo Yamasaki; Hajime Ishikawa; Masayuki Kitano; Takuya Nakai; Yoshifumi Takeyama
Journal:  Clin J Gastroenterol       Date:  2013-03-23

6.  Well-differentiated endocrine tumor of the distal common bile duct: a case study and literature review.

Authors:  Gabriella Nesi; Antonella Lombardi; Giacomo Batignani; Ferdinando Ficari; Carlos A Rubio; Francesco Tonelli
Journal:  Virchows Arch       Date:  2006-05-03       Impact factor: 4.064

7.  Primary neuroendocrine tumors of the main pancreatic duct: a rare entity.

Authors:  Thomas Walter; Valérie Hervieu; Mustapha Adham; Rodica Gincul; Gilles Poncet; Frank Pilleul; Jean-Alain Chayvialle; Christian Partensky; Catherine Lombard-Bohas; Jean-Yves Scoazec
Journal:  Virchows Arch       Date:  2011-03-23       Impact factor: 4.064

8.  Intraductal polypoid lipid-rich neuroendocrine tumor of the pancreas with entrapped ductules: case report and review of the literature.

Authors:  Jaclyn Frances Hechtman; Bernardo Franssen; Daniel M Labow; Ronald E Gordon; Christopher J DiMaio; Eric J Wilck; Gonzalo Carrasco-Avino; Hongfa Zhu
Journal:  Endocr Pathol       Date:  2013-03       Impact factor: 3.943

Review 9.  Pulmonary gangliocytic paraganglioma: a case report and review of the literature.

Authors:  Dongliang Lin; Yanjiao Hu; Xiaoming Xing; Li Ding; Hui Liu; Yujun Li; Fenggang Xiang
Journal:  Int J Clin Exp Pathol       Date:  2013-12-15

10.  Carcinoid Klatskin tumour: A rare cause of obstructive jaundice.

Authors:  Suhail Khuroo; Arshad Rashid; Rajandeep Singh Bali; Majid Mushtaque; Farzana Khuroo
Journal:  Australas Med J       Date:  2014-06-30
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.