A Review of the Clinical Presentation, Outcomes, and Treatments of Patients Having Desmoid Tumors-Reference-Cited by-同舟云学术

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A Review of the Clinical Presentation, Outcomes, and Treatments of Patients Having Desmoid Tumors

Published:2023 Issue:4 Volume:2 Page:588-600
ISSN:2772-5723
Container-title:Gastro Hep Advances
language:en
Short-container-title:Gastro Hep Advances

Author:

Figueredo Carlos^ORCID,Schiano Thomas

Publisher

Elsevier BV

Reference44 articles.

1. The fibromatoses: a clinicopathologic classification based on 140 cases;Allen;Am J Surg Pathol,1977

2. AKT1 and BRAF mutations in pediatric aggressive fibromatosis;Meazza;Cancer Med,2016

3. Desmoid tumor: from surgical extirpation to molecular dissection;Lazar;Curr Opin Oncol,2009

4. Evidence for genetic predisposition to desmoid tumors in familial adenomatous polyposis independent of the germline APC mutation;Sturt;Gut,2004

5. Familial adenomatous polyposis: desmoid tumors and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444;Reiner;Hum Mol Genet,1995

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