Synchronous Fibromatosis Indistinguishable from Suspected Synchronous Gastrointestinal Stromal Tumor: A Case Report

Authors

  • Anup Chalise Department of Surgery, Nepal Medical College and Teaching Hospital, Attarkhel, Kathmandu, Nepal https://orcid.org/0000-0003-2960-0547
  • Ashish Prasad Rajbhandari Department of Surgery, Nepal Medical College and Teaching Hospital, Attarkhel, Kathmandu, Nepal https://orcid.org/0000-0002-3417-9745
  • Ramesh Dhakhwa Department of Pathology, Kathmandu Medical College and Teaching Hospital, Sinamangal, Kathmandu, Nepal

DOI:

https://doi.org/10.31729/jnma.6516

Keywords:

case report, desmoid, fibromatosis, immunohistochemistry

Abstract

Desmoid tumors most commonly occur in the anterior abdominal wall in approximately 50% of
cases and are locally aggressive. We describe a case of a 38-year-old lady who was investigated as a
case of gastrointestinal tumor. Post-operative immunohistochemistry staining showed the presence
of a synchronous desmoid in the abdominal wall and proximal ileum. Wide local excision remains
the gold-standard of treatment with pharmacotherapeutics and radiotherapy serving as adjuvant or
palliative treatment options.

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Published

2021-09-11

How to Cite

Chalise, A., Rajbhandari, A. P., & Dhakhwa, R. (2021). Synchronous Fibromatosis Indistinguishable from Suspected Synchronous Gastrointestinal Stromal Tumor: A Case Report. Journal of Nepal Medical Association, 59(241), 919–921. https://doi.org/10.31729/jnma.6516

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