نتایج جستجو برای: desmoid

تعداد نتایج: 1367  

Journal: :Current oncology 2014
M Ghert X Yao T Corbett A A Gupta R A Kandel S Verma J Werier

OBJECTIVES We set out to determine the optimal treatment options-surgery, radiation therapy (rt), systemic therapy, or any combinations thereof-for patients with desmoid tumours once the decision to undergo active treatment has been made (that is, monitoring and observation have been determined to be inadequate).provide clinical-expert consensus opinions on follow-up strategies in patients with...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2011
Mrinal M Gounder Robert A Lefkowitz Mary Louise Keohan David R D'Adamo Meera Hameed Cristina R Antonescu Samuel Singer Katherine Stout Linda Ahn Robert G Maki

BACKGROUND Desmoid tumors (deep fibromatoses) are clonal connective tissue malignancies that do not metastasize, but have a significant risk of local recurrence, and are associated with morbidity and occasionally mortality. Responses of desmoid patients to sorafenib on an expanded access program led us to review our experience. METHODS After Institutional Review Board (IRB) approval, we revie...

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2013

Journal: :European Journal of Cardio-Thoracic Surgery 2018

Journal: :Journal of the Belgian Society of Radiology 2015

Journal: :The Boston Medical and Surgical Journal 1907

2011
Els Robanus-Maandag Cathy Bosch Saeid Amini-Nik Jeroen Knijnenburg Karoly Szuhai Pascale Cervera Raymond Poon Diana Eccles Paolo Radice Marco Giovannini Benjamin A. Alman Sabine Tejpar Peter Devilee Riccardo Fodde

Desmoid tumours (also called deep or aggressive fibromatoses) are potentially life-threatening fibromatous lesions. Hereditary desmoid tumours arise in individuals affected by either familial adenomatous polyposis (FAP) or hereditary desmoid disease (HDD) carrying germline mutations in APC. Most sporadic desmoids carry somatic mutations in CTNNB1. Previous studies identified losses on 5q and 6q...

Journal: :Balkan medical journal 2016
Şefika Arzu Ergen Elif Eda Tiken Didem Çolpan Öksüz Fazilet Öner Dinçbaş Sergülen Dervişoğlu Nil Molinas Mandel Murat Hız Sedat Koca

BACKGROUND Desmoid tumors are uncommon and benign mesenchymal neoplasms. The optimal treatment of patients with desmoid tumors is still controversial. Surgery is the primary treatment for locally invasive or recurrent desmoid tumors. Also, radiotherapy is a treatment option for patients at high risk for local failure such as those with positive margins or recurrent and unresectable tumors. AI...

2014
Shunsuke Hamada Naohisa Futamura Kunihiro Ikuta Hiroshi Urakawa Eiji Kozawa Naoki Ishiguro Yoshihiro Nishida

We hypothesized that patterns of CTNNB1 (β-catenin) mutations would affect the outcome of conservative therapy in patients with desmoid tumors. This study aimed to determine the significance of CTNNB1 (β-catenin) mutations in predicting the treatment outcome in patients with desmoid tumors treated with meloxicam, a cyclooxygenase-2 (COX-2) selective inhibitor. Between 2003 and 2012, consecutive...

2012
Yoshihiro Nishida Satoshi Tsukushi Yoji Shido Hiroshi Urakawa Eisuke Arai Naoki Ishiguro

Treatment modalities for desmoid tumors have been changed because of the high recurrence rate, even after wide resection, and some cases experience spontaneous self-regression during clinical course. The treatment modality in our institutions before 2003 was surgical resection with wide surgical margin, however, meloxicam, which is a NSAID and a selective COX-2 inhibitor has been applied consec...

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