Results 131 to 140 of about 534,321 (261)

Ewing sarcoma in a child with neurofibromatosis type 1. [PDF]

, 2019
We report here on a case of Ewing sarcoma (ES) occurring in a child with neurofibromatosis type 1. The sarcoma had an EWSR1-ERG translocation as well as loss of the remaining wild-type allele of NF1. Loss of the NF1 wild-type allele in the tumor suggests
Bastian, Boris C, Fernandez, Karen S, Hardee, Steven, Horvai, Andrew, Shah, Avanthi Tayi, Sweet-Cordero, E Alejandro, Turski, Michelle L   +6 more
core  

Rare chondrosarcoma of the breast treated with quadrantectomy instead of mastectomy. A case report [PDF]

, 2014
Breast chondrosarcoma is a rare sarcoma that mainly occurs in females >50 years old. To the best of our knowledge, only 16 cases were reported in the literature prior to 2013 and all patients were surgically treated by mastectomy, with or without ...
Badyal, Baldini, Beltaos, Bhosale, DANIELA SOTTILE, De Padua, Demetri, Errarhay, Faraht, FILIPPO CUSTURERI, Gupta, Gupta, Gurleyik, Guymar, Kennedy, Lakshmikantha, Lewin, LUCA DEL VECCHIO, Mujtaba, PAOLO URCIUOLI, Pasta, Patterson, Pencavel, Rakha, Rao, Stojadinovic, Thilagavathi, VALERIO D’ORAZI, Vera-Sempere, Verfaillie, VITTORIO PASTA, Zelek   +31 more
core   +2 more sources

SARCOMA OF THE BREAST [PDF]

Annals of Surgery, 1909
n ...
openaire   +3 more sources

Guillain-Barre syndrome observed with adoptive transfer of lymphocytes genetically engineered with an NY-ESO-1 reactive T-cell receptor

Journal for ImmunoTherapy of Cancer, 2019
Background Adoptive transfer of autologous T-lymphocytes transduced with a high affinity NY-ESO-1-reactive T-cell receptor (NY-ESO-1c259 T-cells) has emerged as a promising therapeutic strategy for patients with refractory synovial sarcoma.
Jocelyn Joseph, Michael J. Nathenson, Van Anh Trinh, Karan Malik, Erica Nowell, Kristen Carter, Shiao-Pei Weathers, George D. Demetri, Dejka Araujo, Anthony P. Conley   +9 more
doaj   +1 more source

Multi-Modality Information Fusion for Radiomics-based Neural Architecture Search [PDF]

arXiv, 2020
'Radiomics' is a method that extracts mineable quantitative features from radiographic images. These features can then be used to determine prognosis, for example, predicting the development of distant metastases (DM). Existing radiomics methods, however, require complex manual effort including the design of hand-crafted radiomic features and their ...
arxiv  

Phase 2 study of dasatinib in patients with alveolar soft part sarcoma, chondrosarcoma, chordoma, epithelioid sarcoma, or solitary fibrous tumor

Cancer, 2017
Alveolar soft part sarcoma (ASPS), chondrosarcoma (CS), chordoma, epithelioid sarcoma, and solitary fibrous tumor (SFT) are malignant tumors that are relatively resistant to chemotherapy and for which more effective drug therapy is needed.
S. Schuetze, V. Bolejack, E. Choy, K. Ganjoo, A. Staddon, W. Chow, H. Tawbi, B. Samuels, Shreyaskumar R Patel, M. Mehren, G. D'Amato, K. Leu, D. Loeb, C. Forscher, M. Milhem, D. Rushing, D. Lucas, R. Chugh, D. Reinke, L. Baker   +19 more
semanticscholar   +1 more source

Pediatric sarcomas.

Oncology letters, 2018
[This retracts the article DOI: 10.3892/ol.2017.7467.].
Cao, Junhua, An, Qi, Wang, Lei
openaire   +3 more sources

An innovative staged prosthetic lengthening reconstruction strategy for osteosarcoma-related leg discrepancy

Scientific Reports
Correction of leg length discrepancy (LLD) in skeletally mature patients with osteosarcoma was rarely reported and quite challenging. This study aimed to propose a treatment strategy of staged lengthening and reconstruction with a standard static ...
Hairong Xu, Yuan Li, Feng Yu, Weifeng Liu, Lin Hao, Qing Zhang, Xiaohui Niu   +6 more
doaj   +1 more source

PDL1 expression is a poor-prognosis factor in soft-tissue sarcomas

OncoImmunology, 2017
Soft-tissue sarcomas (STS) are a group of rare, heterogeneous, and aggressive tumors, with high metastatic risk and relatively few efficient systemic therapies.
François Bertucci, Pascal Finetti, Delphine Perrot, Agnès Leroux, Françoise Collin, Axel Le Cesne, Jean-Michel Coindre, Jean-Yves Blay, Daniel Birnbaum, Emilie Mamessier   +9 more
doaj   +1 more source

Exploring visual language models as a powerful tool in the diagnosis of Ewing Sarcoma [PDF]

arXiv
Ewing's sarcoma (ES), characterized by a high density of small round blue cells without structural organization, presents a significant health concern, particularly among adolescents aged 10 to 19. Artificial intelligence-based systems for automated analysis of histopathological images are promising to contribute to an accurate diagnosis of ES. In this
arxiv