Results 21 to 30 of about 13,029 (233)

Desmoid Tumours in Familial Adenomatous Polyposis: Review of 17 Patients from a Portuguese Tertiary Center [PDF]

open access: yes, 2016
INTRODUCTION: Desmoid Tumours (DT) are benign tumours with an estimated incidence of 2-4 per million per year. Between 7-16% of them are associated with Familial Adenomatous Polyposis (FAP) and are mostly parietal or intra-abdominal.
Martins, V.   +3 more
core   +1 more source

The initiation, design, and establishment of the Desmoid Tumor Research Foundation Patient Registry and Natural History Study

open access: yesRare Tumors, 2019
Desmoid tumors are locally invasive sarcoma, affecting 5–6 individuals out of 1,000,000 per year. The desmoid tumors have high rates of recurrence after resection and can lead to significant deterioration of the quality of life of patients.
Kelly A Mercier, Darragh M Walsh
doaj   +1 more source

Gene Expression Profiling in Familial Adenomatous Polyposis Adenomas and Desmoid Disease [PDF]

open access: yes, 2007
Gene expression profiling is a powerful method by which alterations in gene expression can be interrogated in a single experiment. The disease familial adenomatous polyposis (FAP) is associated with germline mutations in the APC gene, which result in ...
Nikola A Bowden   +2 more
core   +1 more source

Intrathoracic Desmoid Tumor

open access: yesJournal of the Belgian Society of Radiology, 2015
A 47-year-old female was referred to the hospital because of persistent pain at the ventral right side of the chest for several weeks. Except for ankylosing spondylitis, her medical history was insignificant. The patient doesn’t smoke and there is no history of thoracic trauma or surgery. There were no alarm symptoms.
D’Hooghe, L   +4 more
openaire   +5 more sources

Small bowel obstruction caused by a fast‐growing desmoid tumor

open access: yesClinical Case Reports, 2020
Desmoid tumors are rare tumors which can cause intestinal obstructions. Surgical wide excision is currently the treatment of choice, with the goal of achieving free resection margins.
David Martin   +3 more
doaj   +1 more source

Desmoid tumor initially unresectable – About two cases [PDF]

open access: yesIranian Journal of Colorectal Research, 2019
Desmoid tumor, also called aggressive fibromatosis, is a rare fibroblastic proliferation of connective tissue and skeletal muscle aponeurosis. The aetiology of desmoid tumours is poorly understood, but they have been related with oestrogen stimuli ...
Sara Senti Farraraons   +4 more
doaj   +1 more source

Post-traumatic soft tissue tumors: Case report and review of the literature a propos a Post-traumatic paraspinal desmoid tumor [PDF]

open access: yes, 2008
Background Antecedent trauma has been implicated in the causation of soft tissue tumors. Several criteria have been established to define a cause-and-effect relationship.
Gutman Haim   +3 more
core   +2 more sources

Subsequent Development of Desmoid Tumor after a Resected Gastrointestinal Stromal Tumor

open access: yesCase Reports in Pathology, 2018
Desmoid tumors (deep fibromatosis) of the mesentery are rare mesenchymal tumors. They are often misdiagnosed, especially with a previous history of resection for gastrointestinal stromal tumor (GIST).
Areen Abdulelah Murshid   +1 more
doaj   +1 more source

An update on the management of sporadic desmoid-type fibromatosis: A European Consensus Initiative between Sarcoma PAtients EuroNet (SPAEN) and European Organization for Research and Treatment of Cancer (EORTC)/Soft Tissue and Bone Sarcoma Group (STBSG) [PDF]

open access: yes, 2017
Desmoid-type fibromatosis is a rare and locally aggressive monoclonal, fibroblastic proliferation characterized by a variable and often unpredictable clinical course.
Bauer, S. (Sebastian)   +31 more
core   +2 more sources

A massive abdominal wall desmoid tumor occurring in a laparotomy scar: A case report [PDF]

open access: yes, 2011
Introduction Desmoid tumors are benign but locally aggressive tumors of mesenchymal origin which are poorly circumscribed, infiltrate the surrounding tissue, lack a true capsule and are composed of abundant collagen.
Joseph K Wanjeri, Collins JO Opeya
core   +2 more sources

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