Abstract

Desmoid tumors, also known as desmoid-type fibromatosis (DF), develop from musculoaponeurotic tissues. They are Mesenchymal tumorfibrous tumors of benign character that do not metastasize. However, they can take an aggressive course by showing local growth in the area where they are located. Although they can originate fromany skeletal muscle, they are most commonly seen on the anterior abdominal wall. Various treatment options are available depending on the clinical condition of the patient. We aimed to discuss the diagnosis and treatment of DF with a 55-year-old male patient who has DF and applied to our clinic.

Keywords: Mesenchymal tumor, fibrous type, local growth

Copyright and license

Copyright © 2025 The Author(s). This is an open-access article published by Bolu İzzet Baysal Training and Research Hospital under the terms of the Creative Commons Attribution License (CC BY) which permits unrestricted use, distribution, and reproduction in any medium or format, provided the original work is properly cited.

How to cite

1.
Küçüköztaş N, Başaran E, Eksert YE, Dereli M. A rare case report: desmoid-type fibromatosis. Northwestern Med J. 2025;5(1):56-9. https://doi.org/10.54307/2025.NWMJ.178

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