The Landmark Series: Desmoid
Author:
Publisher
Springer Science and Business Media LLC
Subject
Oncology,Surgery
Link
http://link.springer.com/content/pdf/10.1245/s10434-020-09395-5.pdf
Reference53 articles.
1. WHO Classification of Tumours Editorial Board. Soft tissue and bone tumours. 5th Edition. Lyon: International Agency for Research on Cancer; 2020.
2. Fiore M, Rimareix F, Mariani L et al. Desmoid-type fibromatosis: a front-line conservative approach to select patients for surgical treatment. Ann Surg Oncol 2009;16:2587–2593.
3. Bonvalot S, Eldweny H, Haddad V et al. Extra-abdominal primary fibromatosis: Aggressive management could be avoided in a subgroup of patients. Eur J Surg Oncol 2008;34:462–468.
4. Timbergen MJM, Schut AW, Grunhagen DJ, Sleijfer S, Verhoef C. Active surveillance in desmoid-type fibromatosis: a systematic literature review. Eur J Cancer 2020;137:18–29.
5. Penel N, Le Cesne A, Bonvalot S et al. Surgical versus non-surgical approach in primary desmoid-type fibromatosis patients: a nationwide prospective cohort from the French Sarcoma Group. Eur J Cancer 2017;83:125–131.
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1. Efficacy and safety of anlotinib in patients with desmoid fibromatosis: a retrospective analysis;Frontiers in Oncology;2024-05-14
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5. Disease and economic burden of surgery in desmoid tumors: a review;Expert Review of Pharmacoeconomics & Outcomes Research;2023-04-26
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