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Metastatic gastric adenocarcinoma and synchronous carcinoid tumour mimicking appendicitis: A case report

INTRODUCTION: Silent metastatic gastric adenocarcinoma presenting as appendicitis is very rare. Rare pathologies may be encountered during common operations such as appendicectomy and an awareness of possible alternative pathological entities would be helpful in a surgeon’s wealth of knowledge. PRES...

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Autores principales: Tran, Q.B., Mizumoto, R., Ratnayake, S., Strekozov, B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5856669/
https://www.ncbi.nlm.nih.gov/pubmed/29482082
http://dx.doi.org/10.1016/j.ijscr.2018.02.023
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author Tran, Q.B.
Mizumoto, R.
Ratnayake, S.
Strekozov, B.
author_facet Tran, Q.B.
Mizumoto, R.
Ratnayake, S.
Strekozov, B.
author_sort Tran, Q.B.
collection PubMed
description INTRODUCTION: Silent metastatic gastric adenocarcinoma presenting as appendicitis is very rare. Rare pathologies may be encountered during common operations such as appendicectomy and an awareness of possible alternative pathological entities would be helpful in a surgeon’s wealth of knowledge. PRESENTATION OF CASE: A 63-year-old man presented with a three-day history of acute abdominal pain suggestive of appendicitis. Intra-operatively, a macroscopically inflamed and perforated appendix was found. There were however some atypical features, which included multiple inflamed ulcerated lesions throughout the small bowel mesentery and along the terminal ileum. Appendicectomy was performed and biopsies of these lesions were taken. Subsequent histopathology revealed that there were metastatic deposits of poorly differentiated adenocarcinoma in the appendix and mesenteric biopsies, as well as a neuroendocrine (carcinoid) tumour of the appendix. Upper endoscopy confirmed a gastric primary leading to peritoneal dissemination. The patient was scheduled to undergo a course of palliative chemotherapy. DISCUSSION: Metastatic gastric adenocarcinomas with peritoneal dissemination have a very poor prognosis and often the first choice of treatment is chemotherapy as a complete cure through surgery is often not feasible. As for classical carcinoid tumours smaller than 2 cm towards the tip of the appendix with low proliferative index and without angiolymphatic or mesoappendiceal extension, then appendicectomy alone is indicated. Synchronous neoplastic pathologies presenting as appendicitis is largely unknown. CONCLUSION: To our knowledge, this is the first report in the literature of synchronous carcinoid tumour and metastatic gastric cancer co-existing within an inflamed appendix.
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spelling pubmed-58566692018-03-19 Metastatic gastric adenocarcinoma and synchronous carcinoid tumour mimicking appendicitis: A case report Tran, Q.B. Mizumoto, R. Ratnayake, S. Strekozov, B. Int J Surg Case Rep Article INTRODUCTION: Silent metastatic gastric adenocarcinoma presenting as appendicitis is very rare. Rare pathologies may be encountered during common operations such as appendicectomy and an awareness of possible alternative pathological entities would be helpful in a surgeon’s wealth of knowledge. PRESENTATION OF CASE: A 63-year-old man presented with a three-day history of acute abdominal pain suggestive of appendicitis. Intra-operatively, a macroscopically inflamed and perforated appendix was found. There were however some atypical features, which included multiple inflamed ulcerated lesions throughout the small bowel mesentery and along the terminal ileum. Appendicectomy was performed and biopsies of these lesions were taken. Subsequent histopathology revealed that there were metastatic deposits of poorly differentiated adenocarcinoma in the appendix and mesenteric biopsies, as well as a neuroendocrine (carcinoid) tumour of the appendix. Upper endoscopy confirmed a gastric primary leading to peritoneal dissemination. The patient was scheduled to undergo a course of palliative chemotherapy. DISCUSSION: Metastatic gastric adenocarcinomas with peritoneal dissemination have a very poor prognosis and often the first choice of treatment is chemotherapy as a complete cure through surgery is often not feasible. As for classical carcinoid tumours smaller than 2 cm towards the tip of the appendix with low proliferative index and without angiolymphatic or mesoappendiceal extension, then appendicectomy alone is indicated. Synchronous neoplastic pathologies presenting as appendicitis is largely unknown. CONCLUSION: To our knowledge, this is the first report in the literature of synchronous carcinoid tumour and metastatic gastric cancer co-existing within an inflamed appendix. Elsevier 2018-02-16 /pmc/articles/PMC5856669/ /pubmed/29482082 http://dx.doi.org/10.1016/j.ijscr.2018.02.023 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Tran, Q.B.
Mizumoto, R.
Ratnayake, S.
Strekozov, B.
Metastatic gastric adenocarcinoma and synchronous carcinoid tumour mimicking appendicitis: A case report
title Metastatic gastric adenocarcinoma and synchronous carcinoid tumour mimicking appendicitis: A case report
title_full Metastatic gastric adenocarcinoma and synchronous carcinoid tumour mimicking appendicitis: A case report
title_fullStr Metastatic gastric adenocarcinoma and synchronous carcinoid tumour mimicking appendicitis: A case report
title_full_unstemmed Metastatic gastric adenocarcinoma and synchronous carcinoid tumour mimicking appendicitis: A case report
title_short Metastatic gastric adenocarcinoma and synchronous carcinoid tumour mimicking appendicitis: A case report
title_sort metastatic gastric adenocarcinoma and synchronous carcinoid tumour mimicking appendicitis: a case report
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5856669/
https://www.ncbi.nlm.nih.gov/pubmed/29482082
http://dx.doi.org/10.1016/j.ijscr.2018.02.023
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AT strekozovb metastaticgastricadenocarcinomaandsynchronouscarcinoidtumourmimickingappendicitisacasereport