A rare case report: desmoid-type fibromatosis
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. Althou...
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| Format: | Article |
| Language: | English |
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Izzet Baysal Training and Research Hospital
2025-01-01
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| Series: | Northwestern Medical Journal |
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| Online Access: | https://nwmedj.org/article/view/178 |
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| author | Nadire Küçüköztaş Elif Başaran Yunus Emre Eksert Melike Dereli |
| author_facet | Nadire Küçüköztaş Elif Başaran Yunus Emre Eksert Melike Dereli |
| author_sort | Nadire Küçüköztaş |
| collection | DOAJ |
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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.
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| format | Article |
| id | doaj-art-67d67dcc347149ce9ac3ffb854985b65 |
| institution | Kabale University |
| issn | 2979-9538 |
| language | English |
| publishDate | 2025-01-01 |
| publisher | Izzet Baysal Training and Research Hospital |
| record_format | Article |
| series | Northwestern Medical Journal |
| spelling | doaj-art-67d67dcc347149ce9ac3ffb854985b652025-02-04T12:17:07ZengIzzet Baysal Training and Research HospitalNorthwestern Medical Journal2979-95382025-01-015110.54307/2025.NWMJ.178A rare case report: desmoid-type fibromatosisNadire Küçüköztaş0https://orcid.org/0000-0001-5588-0306Elif Başaran1https://orcid.org/0000-0001-8367-0242Yunus Emre Eksert2https://orcid.org/0000-0003-0961-9443Melike Dereli3https://orcid.org/0009-0002-2596-0502Department of Medical Oncology, Faculty of Medicine, Bolu Abant İzzet Baysal University, Bolu, TürkiyeDepartment of Internal Medicine, Faculty of Medicine, Bolu Abant İzzet Baysal University, Bolu, TürkiyeFaculty of Medicine, Bolu Abant İzzet Baysal University, Bolu, TürkiyeFaculty of Medicine, Bolu Abant İzzet Baysal University, Bolu, Türkiye 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. https://nwmedj.org/article/view/178Mesenchymal tumorfibrous typelocal growth |
| spellingShingle | Nadire Küçüköztaş Elif Başaran Yunus Emre Eksert Melike Dereli A rare case report: desmoid-type fibromatosis Northwestern Medical Journal Mesenchymal tumor fibrous type local growth |
| title | A rare case report: desmoid-type fibromatosis |
| title_full | A rare case report: desmoid-type fibromatosis |
| title_fullStr | A rare case report: desmoid-type fibromatosis |
| title_full_unstemmed | A rare case report: desmoid-type fibromatosis |
| title_short | A rare case report: desmoid-type fibromatosis |
| title_sort | rare case report desmoid type fibromatosis |
| topic | Mesenchymal tumor fibrous type local growth |
| url | https://nwmedj.org/article/view/178 |
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