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Desmoid-type fibromatosis: imaging features and course
Miho Okuda1, Kotaro Yoshida2, Satoshi Kobayashi3
1Department of Radiology, Kanazawa University Hospital, 13-1 Takaramachi, Kanazawa, 920-8640, Japan. okudamiho@staff.kanazawa-u.ac.jp.
Desmoid-type fibromatosis (DF) is a rare soft tissue tumor. This review focuses on imaging features of DF, particularly spontaneous regression and changes after treatment, guiding current surveillance strategies.
Area of Science:
- Oncology
- Radiology
- Soft Tissue Pathology
Background:
- Desmoid-type fibromatosis (DF) presents as an infiltrative soft tissue tumor with high local recurrence rates.
- DF exhibits unpredictable behavior, including spontaneous regression, leading to evolving treatment paradigms.
- Active surveillance is increasingly adopted as the primary management strategy for DF.
Purpose of the Study:
- To review and characterize the imaging features of desmoid-type fibromatosis.
- To correlate imaging findings with the clinical course of DF, including regression and postoperative changes.
- To analyze imaging alterations following systemic treatment for DF.
Main Methods:
- Retrospective review of imaging studies in patients diagnosed with DF.
- Analysis of imaging features in cases of spontaneous regression.
- Evaluation of imaging changes in postoperative DF and after systemic therapy.
Main Results:
- Imaging findings associated with spontaneous regression of DF were identified.
- Characteristic postoperative imaging changes were documented.
- Radiological evidence of tumor response to systemic treatments was observed.
Conclusions:
- Imaging plays a crucial role in monitoring the unpredictable course of DF.
- Understanding imaging features aids in managing DF, especially in the context of surveillance and treatment response.
- Radiological assessment is vital for guiding therapeutic decisions and evaluating outcomes in DF.
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