Desmoid tumours are rare, myofibroblastic, soft tissue tumours. However, in the context of familial adenomatous polyposis, they can affect up to a quarter of patients. Desmoid tumours remain the most significant extra-intestinal manifestation of this cancer predisposing, autosomal dominant, condition. Due to their rarity, and unusual growth behaviour, studying these tumours remains a challenge. The clinical studies in this thesis aimed to highlight the complications associated with desmoid tumours and their impact on patient quality of life. The laboratory studies sought to identify potential pathways involved in their growth and detect genetic variants that may influence this process. A retrospective cohort study identified a 25% risk o...
Desmoid tumours (also called deep or aggressive fibromatoses) are potentially life-threatening fibro...
BACKGROUND: Many patients with familial adenomatous polyposis (FAP) die from desmoid tumours which c...
Desmoids tumors, characterized by monoclonal proliferation of myofibroblasts, could occur in 5-10% o...
Desmoid tumours (DT) are rare myofibroblastic monoclonal proliferations, which are present in 10-25 ...
© 2018 Dr. Timothy ChittleboroughDesmoid tumour is a benign growth that causes morbidity and mortali...
Familial adenomatous polyposis (FAP) is a cancer syndrome caused by a germline mutation in the adeno...
Background & Aims: Desmoid tumors are a severe extracolonic manifestation in familial adenomatous po...
Background & Aims: Desmoid tumors are a severe extracolonic manifestation in familial adenomatous po...
BACKGROUND & AIMS: Desmoid tumors are a severe extracolonic manifestation in familial adenomatous po...
Background: Desmoid tumors are a group of benign, invasive, solid tumors that are relatively rare in...
Extra-abdominal desmoid tumors are a significant cause of morbidity in patients with familial adenom...
Introduction: Desmoid tumours are locally aggressive tumours which are common in Familial Adenomatou...
Background: Germline mutations of the APC tumour suppressor gene on chromosome 5q22 are responsible...
Introduction: Abdominal desmoid tumors are locally aggressive tumors that develop in familial adenom...
BACKGROUND: Ability to identify patients with familial adenomatous polyposis who have a high risk of...
Desmoid tumours (also called deep or aggressive fibromatoses) are potentially life-threatening fibro...
BACKGROUND: Many patients with familial adenomatous polyposis (FAP) die from desmoid tumours which c...
Desmoids tumors, characterized by monoclonal proliferation of myofibroblasts, could occur in 5-10% o...
Desmoid tumours (DT) are rare myofibroblastic monoclonal proliferations, which are present in 10-25 ...
© 2018 Dr. Timothy ChittleboroughDesmoid tumour is a benign growth that causes morbidity and mortali...
Familial adenomatous polyposis (FAP) is a cancer syndrome caused by a germline mutation in the adeno...
Background & Aims: Desmoid tumors are a severe extracolonic manifestation in familial adenomatous po...
Background & Aims: Desmoid tumors are a severe extracolonic manifestation in familial adenomatous po...
BACKGROUND & AIMS: Desmoid tumors are a severe extracolonic manifestation in familial adenomatous po...
Background: Desmoid tumors are a group of benign, invasive, solid tumors that are relatively rare in...
Extra-abdominal desmoid tumors are a significant cause of morbidity in patients with familial adenom...
Introduction: Desmoid tumours are locally aggressive tumours which are common in Familial Adenomatou...
Background: Germline mutations of the APC tumour suppressor gene on chromosome 5q22 are responsible...
Introduction: Abdominal desmoid tumors are locally aggressive tumors that develop in familial adenom...
BACKGROUND: Ability to identify patients with familial adenomatous polyposis who have a high risk of...
Desmoid tumours (also called deep or aggressive fibromatoses) are potentially life-threatening fibro...
BACKGROUND: Many patients with familial adenomatous polyposis (FAP) die from desmoid tumours which c...
Desmoids tumors, characterized by monoclonal proliferation of myofibroblasts, could occur in 5-10% o...