The dilemma in management of desmoid tumour: A case report

Introduction: Desmoid tumours are rare benign tumours. The tumours may develop sporadically or they may be linked to familial adenomatous polyposis (FAP) in Gardner’s syndrome. Aim: This article highlights a young lady with an intra-abdominal desmoid tumour that manifested as an acute abdomen and we...

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Main Authors: Fei, Yee Lee, Arvind Vashdev Jagwani, Mohamad Fairuz Mohamad Sharin, Andee Dzulkarnain Zakaria, Mohd Firdaus Mohd Hayati, Ismail Sagap
Format: Article
Language:English
English
Published: Collegium Medicum University of Warmia and Mazury 2022
Subjects:
Online Access:https://eprints.ums.edu.my/id/eprint/34362/1/FULL%20TEXT.pdf
https://eprints.ums.edu.my/id/eprint/34362/3/ABSTRACT.pdf
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author Fei, Yee Lee
Arvind Vashdev Jagwani
Mohamad Fairuz Mohamad Sharin
Andee Dzulkarnain Zakaria
Mohd Firdaus Mohd Hayati
Ismail Sagap
author_facet Fei, Yee Lee
Arvind Vashdev Jagwani
Mohamad Fairuz Mohamad Sharin
Andee Dzulkarnain Zakaria
Mohd Firdaus Mohd Hayati
Ismail Sagap
author_sort Fei, Yee Lee
collection UMS
description Introduction: Desmoid tumours are rare benign tumours. The tumours may develop sporadically or they may be linked to familial adenomatous polyposis (FAP) in Gardner’s syndrome. Aim: This article highlights a young lady with an intra-abdominal desmoid tumour that manifested as an acute abdomen and we discuss our management strategy. Case study: A 24-year-old lady with a known FAP who had undergone a pan A 24-year-old lady with a known FAP who had undergone a panproctocolectomy with an ileal pouch-anal anastomosis and total thyroidectomy, later was complicated with acute abdomen for symptomatic desmoid tumour. Computed tomography of the abdomen showed a large intraperitoneal heterogenous mass with small bowel displacement and was confirmed by magnetic resonance imaging. An exploratory laparotomy and en-bloc resection of the tumour with an end ileostomy were performed. Results and discussion: Intra-abdominal desmoid tumours usually pre Intra-abdominal desmoid tumours usually present as a painless slow-growing mass, however, in severe form, it can cause bowel ischemia, intestinal obstruction, or deterioration of function in the ileoanal anastomosis, among post total colectomy. Surgery is indicated upfront in specific clinical scenarios namely complications (occlusion, perforation, or bleeding) or major cosmetic issues. Conclusions: Desmoid tumour, despite being benign, is challenging to manage due to its compressing nature. As a key point, the diagnosis of a desmoid tumour should be suspected and followed up closely in patients with a previous history of FAP in combination with extracolonic manifestation.
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spelling ums.eprints-343622022-10-11T04:35:43Z https://eprints.ums.edu.my/id/eprint/34362/ The dilemma in management of desmoid tumour: A case report Fei, Yee Lee Arvind Vashdev Jagwani Mohamad Fairuz Mohamad Sharin Andee Dzulkarnain Zakaria Mohd Firdaus Mohd Hayati Ismail Sagap RD520-599.5 Surgery by region, system, or organ Introduction: Desmoid tumours are rare benign tumours. The tumours may develop sporadically or they may be linked to familial adenomatous polyposis (FAP) in Gardner’s syndrome. Aim: This article highlights a young lady with an intra-abdominal desmoid tumour that manifested as an acute abdomen and we discuss our management strategy. Case study: A 24-year-old lady with a known FAP who had undergone a pan A 24-year-old lady with a known FAP who had undergone a panproctocolectomy with an ileal pouch-anal anastomosis and total thyroidectomy, later was complicated with acute abdomen for symptomatic desmoid tumour. Computed tomography of the abdomen showed a large intraperitoneal heterogenous mass with small bowel displacement and was confirmed by magnetic resonance imaging. An exploratory laparotomy and en-bloc resection of the tumour with an end ileostomy were performed. Results and discussion: Intra-abdominal desmoid tumours usually pre Intra-abdominal desmoid tumours usually present as a painless slow-growing mass, however, in severe form, it can cause bowel ischemia, intestinal obstruction, or deterioration of function in the ileoanal anastomosis, among post total colectomy. Surgery is indicated upfront in specific clinical scenarios namely complications (occlusion, perforation, or bleeding) or major cosmetic issues. Conclusions: Desmoid tumour, despite being benign, is challenging to manage due to its compressing nature. As a key point, the diagnosis of a desmoid tumour should be suspected and followed up closely in patients with a previous history of FAP in combination with extracolonic manifestation. Collegium Medicum University of Warmia and Mazury 2022 Article PeerReviewed text en https://eprints.ums.edu.my/id/eprint/34362/1/FULL%20TEXT.pdf text en https://eprints.ums.edu.my/id/eprint/34362/3/ABSTRACT.pdf Fei, Yee Lee and Arvind Vashdev Jagwani and Mohamad Fairuz Mohamad Sharin and Andee Dzulkarnain Zakaria and Mohd Firdaus Mohd Hayati and Ismail Sagap (2022) The dilemma in management of desmoid tumour: A case report. Polish Annals of Medicine. pp. 1-4. ISSN 1230-8013 http://www.paom.pl/pdf-150516-80425?filename=The%20dilemma%20in%20management.pdf https://doi.org/10.29089/paom/150516 https://doi.org/10.29089/paom/150516
spellingShingle RD520-599.5 Surgery by region, system, or organ
Fei, Yee Lee
Arvind Vashdev Jagwani
Mohamad Fairuz Mohamad Sharin
Andee Dzulkarnain Zakaria
Mohd Firdaus Mohd Hayati
Ismail Sagap
The dilemma in management of desmoid tumour: A case report
title The dilemma in management of desmoid tumour: A case report
title_full The dilemma in management of desmoid tumour: A case report
title_fullStr The dilemma in management of desmoid tumour: A case report
title_full_unstemmed The dilemma in management of desmoid tumour: A case report
title_short The dilemma in management of desmoid tumour: A case report
title_sort dilemma in management of desmoid tumour a case report
topic RD520-599.5 Surgery by region, system, or organ
url https://eprints.ums.edu.my/id/eprint/34362/1/FULL%20TEXT.pdf
https://eprints.ums.edu.my/id/eprint/34362/3/ABSTRACT.pdf
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