2019
DOI: 10.1002/jso.25676
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Screening populations at high risk for soft tissue sarcoma and surveillance following soft tissue sarcoma resection

Abstract: Soft tissue sarcomas (STS) are a rare and diverse group of tumors that affect both adult and pediatric populations. This review discusses current screening recommendations for populations at increased risk for STS, including those with genetic predispositions. We also review surveillance guidelines for those at risk for recurrence following curative-intent surgery. K E Y W O R D S diagnostic screening programs, hereditary neoplastic syndromes, sarcoma, surveillance guidelines, surveillance imaging

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Cited by 6 publications
(1 citation statement)
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References 96 publications
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“…Another group investigated diffusion-weighted MRI, claiming that it is more specific, but less sensitive in fining local recurrence than conventional MRI [42]. Several authors propose adjusting the surveillance strategy according to risk of local recurrence [43][44][45]. Distinguishing posttreatment changes from recurrent tumor is a major challenge, which necessitates a systematic approach to imaging, with fixed intervals, and adequate reflection of the patient's clinical and surgical history [46].…”
Section: Discussionmentioning
confidence: 99%
“…Another group investigated diffusion-weighted MRI, claiming that it is more specific, but less sensitive in fining local recurrence than conventional MRI [42]. Several authors propose adjusting the surveillance strategy according to risk of local recurrence [43][44][45]. Distinguishing posttreatment changes from recurrent tumor is a major challenge, which necessitates a systematic approach to imaging, with fixed intervals, and adequate reflection of the patient's clinical and surgical history [46].…”
Section: Discussionmentioning
confidence: 99%