Results 31 to 40 of about 516,933 (343)

Surgery in reference centers improves survival of sarcoma patients: a nationwide study

open access: yesAnnals of Oncology, 2019
Background NETSARC (netsarc.org) is a network of 26 sarcoma reference centers with specialized multidisciplinary tumor boards (MDTB) aiming to improve the outcome of sarcoma patients. Since 2010, presentation to an MDTB and expert pathological review are
J. Blay   +52 more
semanticscholar   +1 more source

Myoepithelial carcinoma with RB1 mutation: remarkable chemosensitivity to carcinoma of unknown origin therapy

open access: yesBMC Cancer, 2017
Background Myoepithelial carcinoma of soft tissue is a rare, malignant neoplasm that is morphologically and immunophenotypically similar to its counterpart in salivary gland.
Timothy M. Hoggard   +9 more
doaj   +1 more source

Focus on sarcomas [PDF]

open access: yesCancer Cell, 2002
In summary, sarcomas represent a heterogeneous group of diseases, each with a unique and complex pathway to carcinogenesis. The challenge of the next decade will be to define sarcomas according to their unique molecular alterations and to treat them accordingly. The implementation of genomic technologies such as microarray analysis will facilitate this
Crystal L. Mackall   +2 more
openaire   +3 more sources

Foreign Body Granulomas Induced by Intramuscular Leuprorelin Acetate Injection for Prostate Cancer: Clinical Mimics of Soft Tissue Sarcoma

open access: yesCase Reports in Oncological Medicine, 2015
We describe two cases of florid, foreign body granulomatous reaction occurring in the upper arms of males in their eighth decade, who were undergoing treatment with depot injection of leuprorelin acetate for prostatic carcinoma.
Khin Thway   +3 more
doaj   +1 more source

Pro-inflammatory effects of human apatite crystals extracted from patients suffering from calcific tendinopathy

open access: yesArthritis Research & Therapy, 2021
Background Calcific tendonitis of the rotator cuff is due to carbonated apatite deposits in the shoulder tendons. During the evolution of the disease, an acute inflammatory episode may occur leading to the disappearance of the calcification.
Julien Herman   +6 more
doaj   +1 more source

Safety and Efficacy of Anlotinib, a Multikinase Angiogenesis Inhibitor, in Patients with Refractory Metastatic Soft-Tissue Sarcoma

open access: yesClinical Cancer Research, 2018
Purpose: The prognosis for patients with refractory soft-tissue sarcoma (STS) is dismal. Anlotinib has previously shown antitumor activity on STS in preclinical and phase I studies.
Y. Chi   +19 more
semanticscholar   +1 more source

Synovial sarcoma: the misdiagnosed sarcoma

open access: yesEFORT Open Reviews
Synovial sarcoma is a rare and highly malignant soft tissue sarcoma. The inconspicuous and diversity of its early symptoms make it a highly misdiagnosed disease. The management of synovial sarcomas is challenging as they are rare and have a poor prognosis. Early and correct diagnosis and treatment are critical for clinical outcomes.
Chengxiang Li   +4 more
openaire   +2 more sources

Sarcoma Immunotherapy [PDF]

open access: yesCancers, 2011
Much of our knowledge regarding cancer immunotherapy has been derived from sarcoma models. However, translation of preclinical findings to bedside success has been limited in this disease, though several intriguing clinical studies hint at the potential efficacy of this treatment modality.
Gouw, Launce G   +3 more
openaire   +3 more sources

Imaging investigations before referral to a sarcoma center delay the final diagnosis of musculoskeletal sarcoma

open access: yesActa Orthopaedica, 2017
Background and purpose — The use of point-of-care or local investigations before referral to specialist sarcoma centers as part of a fast-track diagnostic pathway varies, and may affect the time to diagnosis.
Heidi Buvarp Dyrop   +4 more
doaj   +1 more source

Myoepithelial carcinoma of the paracecal mesentery: aggressive behavior of a rare neoplasm at an unusual anatomic site

open access: yesRare Tumors, 2017
Myoepithelial tumors of the soft tissues represent a rare group of neoplasms that vary in their clinical behavior, pathologic features and genetics. They are histopathologically typified by a myoepithelial immunohistochemical phenotype, of expression of ...
Khin Thway   +4 more
doaj   +1 more source

Home - About - Disclaimer - Privacy