Cargando…

Vanek's tumor as an unusual cause of ileo-ileal intessuception – A unique case report

BACKGROUND AND AIM: Vanek's tumor is a rare solitary lesion that is non-neoplastic, and arises from the submucosa of the gut. The most commonly affected sites are the stomach and the ileum [1]. IFP causing intestinal obstruction is uncommon and that ileo-ileal intussusception has been reported...

Descripción completa

Detalles Bibliográficos
Autores principales: Jan, Zaka Ullah, Muslim, Muhammad, Ullah, Kaleem, Shoaib, Azam, Ahmed, Nisar, Khan, Zainab Mahsal, Aurangzeb, Mahmud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039895/
https://www.ncbi.nlm.nih.gov/pubmed/30002823
http://dx.doi.org/10.1016/j.amsu.2018.06.006
_version_ 1783338762798891008
author Jan, Zaka Ullah
Muslim, Muhammad
Ullah, Kaleem
Shoaib, Azam
Ahmed, Nisar
Khan, Zainab Mahsal
Aurangzeb, Mahmud
author_facet Jan, Zaka Ullah
Muslim, Muhammad
Ullah, Kaleem
Shoaib, Azam
Ahmed, Nisar
Khan, Zainab Mahsal
Aurangzeb, Mahmud
author_sort Jan, Zaka Ullah
collection PubMed
description BACKGROUND AND AIM: Vanek's tumor is a rare solitary lesion that is non-neoplastic, and arises from the submucosa of the gut. The most commonly affected sites are the stomach and the ileum [1]. IFP causing intestinal obstruction is uncommon and that ileo-ileal intussusception has been reported in the literature rarely. We present a case of an ileo-ileal intessuception in a patient who presented with acute on chronic pain abdomen and anorexia. CT abdomen & pelvis revealed a 46 × 36 mm intraluminal mass in the left iliac fossa causing ileo-ileal intussusception. CASE PRESENTATION: A 60 years old gentleman was brought to the A&E with a history of intestinal obstruction. He was examined and admitted to the surgical unit. CBC revealed unique feature of reactive thrombocytosis apart from a low hemoglobin and a raised TLC. His CT scan demonstrated findings of ileo-ileal intussusception. After an informed written consent, patient underwent an exploratory laparotomy and had resection and anastomosis of the bowel. Histopathology of the specimen revealed findings compatible with IFP. Patient made an uneventful recovery post-operatively and was sent home in the next few days. On follow-up, the patient was doing well and had no complaints of abdominal pain or anorexia. CONCLUSION: Vanek's tumor although a rare entity, should be considered in each case of acute abdomen and physicians and surgeons need to have a high degree of suspicion in such cases. Moreover, IFP can cause reactive thrombocytosis that gets resolved after a post-operative period of 6–8 weeks.
format Online
Article
Text
id pubmed-6039895
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-60398952018-07-12 Vanek's tumor as an unusual cause of ileo-ileal intessuception – A unique case report Jan, Zaka Ullah Muslim, Muhammad Ullah, Kaleem Shoaib, Azam Ahmed, Nisar Khan, Zainab Mahsal Aurangzeb, Mahmud Ann Med Surg (Lond) Case Report BACKGROUND AND AIM: Vanek's tumor is a rare solitary lesion that is non-neoplastic, and arises from the submucosa of the gut. The most commonly affected sites are the stomach and the ileum [1]. IFP causing intestinal obstruction is uncommon and that ileo-ileal intussusception has been reported in the literature rarely. We present a case of an ileo-ileal intessuception in a patient who presented with acute on chronic pain abdomen and anorexia. CT abdomen & pelvis revealed a 46 × 36 mm intraluminal mass in the left iliac fossa causing ileo-ileal intussusception. CASE PRESENTATION: A 60 years old gentleman was brought to the A&E with a history of intestinal obstruction. He was examined and admitted to the surgical unit. CBC revealed unique feature of reactive thrombocytosis apart from a low hemoglobin and a raised TLC. His CT scan demonstrated findings of ileo-ileal intussusception. After an informed written consent, patient underwent an exploratory laparotomy and had resection and anastomosis of the bowel. Histopathology of the specimen revealed findings compatible with IFP. Patient made an uneventful recovery post-operatively and was sent home in the next few days. On follow-up, the patient was doing well and had no complaints of abdominal pain or anorexia. CONCLUSION: Vanek's tumor although a rare entity, should be considered in each case of acute abdomen and physicians and surgeons need to have a high degree of suspicion in such cases. Moreover, IFP can cause reactive thrombocytosis that gets resolved after a post-operative period of 6–8 weeks. Elsevier 2018-06-26 /pmc/articles/PMC6039895/ /pubmed/30002823 http://dx.doi.org/10.1016/j.amsu.2018.06.006 Text en © 2018 The Authors. Published by Elsevier Ltd on behalf of IJS Publishing Group Ltd. 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 Case Report
Jan, Zaka Ullah
Muslim, Muhammad
Ullah, Kaleem
Shoaib, Azam
Ahmed, Nisar
Khan, Zainab Mahsal
Aurangzeb, Mahmud
Vanek's tumor as an unusual cause of ileo-ileal intessuception – A unique case report
title Vanek's tumor as an unusual cause of ileo-ileal intessuception – A unique case report
title_full Vanek's tumor as an unusual cause of ileo-ileal intessuception – A unique case report
title_fullStr Vanek's tumor as an unusual cause of ileo-ileal intessuception – A unique case report
title_full_unstemmed Vanek's tumor as an unusual cause of ileo-ileal intessuception – A unique case report
title_short Vanek's tumor as an unusual cause of ileo-ileal intessuception – A unique case report
title_sort vanek's tumor as an unusual cause of ileo-ileal intessuception – a unique case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039895/
https://www.ncbi.nlm.nih.gov/pubmed/30002823
http://dx.doi.org/10.1016/j.amsu.2018.06.006
work_keys_str_mv AT janzakaullah vanekstumorasanunusualcauseofileoilealintessuceptionauniquecasereport
AT muslimmuhammad vanekstumorasanunusualcauseofileoilealintessuceptionauniquecasereport
AT ullahkaleem vanekstumorasanunusualcauseofileoilealintessuceptionauniquecasereport
AT shoaibazam vanekstumorasanunusualcauseofileoilealintessuceptionauniquecasereport
AT ahmednisar vanekstumorasanunusualcauseofileoilealintessuceptionauniquecasereport
AT khanzainabmahsal vanekstumorasanunusualcauseofileoilealintessuceptionauniquecasereport
AT aurangzebmahmud vanekstumorasanunusualcauseofileoilealintessuceptionauniquecasereport