Results 41 to 50 of about 6,148 (193)
Primary mediastinal Ewing’s sarcoma presenting with sudden and severe chest pain: a case report
Frontiers in OncologyEwing’s sarcoma, characterized by small round cell morphology, is a rare malignancy, with mediastinal Ewing’s sarcoma being even less common. This case describes a distinctive presentation of primary mediastinal Ewing’s sarcoma in a 32-year-old male ...
Chen Su +5 more
doaj +1 more source
Gene expression response to EWS–FLI1 in mouse embryonic cartilage
Genomics Data, 2014 Ewing's sarcoma is a rare bone tumor that affects children and adolescents. We have recently succeeded to induce Ewing's sarcoma-like small round cell tumor in mice by expression of EWS–ETS fusion genes in murine embryonic osteochondrogenic progenitors ...
Miwa Tanaka +5 more
doaj +1 more source
SAGE Open Medical Case Reports, 2023 Being the second most common malignant bone tumor in children and young adults, Ewing’s sarcoma can also occur as a primary soft-tissue tumor called extraosseous or extra-skeletal Ewing’s sarcoma.
Yahya El Harras +5 more
doaj +1 more source
Ewing's sarcoma of the hand [PDF]
BMJ Case Reports, 2014 A 54-year-old woman presented with a 12-month history of pain and a firm fixed mass on the dorsum of the right hand (figure 1). Physical examination revealed a firm circumferential swelling of the hand. The laboratory findings were within normal limits. Figure 1 Clinical view showing swelling of the right hand.
Khaled, Bouzaidi +3 more
openaire +2 more sources
The Role of Chemotherapy in Pediatric Myoepithelial Carcinoma: A Systematic Review of the Literature
Pediatric Blood &Cancer, EarlyView.ABSTRACT Myoepithelial carcinoma (MEC) in pediatric patients is a rare and aggressive malignancy characterized by heterogeneous morphology and variable molecular features. The optimal role of chemotherapy remains unclear. We conducted a systematic review according to PRISMA 2020 guidelines to evaluate chemotherapy in pediatric and young‐adult patients ...
Marco Salvi +7 more
wiley +1 more source
Primitive Neuroectodermal Tumor of the Cervix Uteri
International Journal of Hematology-Oncology and Stem Cell Research, 2012 Ewing’s sarcoma is a round cell malignancy of bone and soft tissue that occurs predominately in adolescents and young adults.It is an uncommon malignancy, but is recognized as the second most prevalent primary bone tumor worldwide.
Zineb Benbrahim +5 more
doaj
Latest developments in the pathobiology of Ewing sarcoma
Journal of Bone Oncology, 2022 Ewing's sarcoma (ES) is an aggressive malignant tumor commonly affecting adolescents. The standard of care includes surgical treatment and systemic therapies, although ES patients often develop drug resistance, leading to disease progression ...
Irina Karlina +7 more
doaj +1 more source
Pediatric Blood &Cancer, EarlyView.ABSTRACT Ewing sarcoma (ES) and rhabdomyosarcoma (RMS) are aggressive malignancies in children and adolescents where metastases impact prognosis. 18F‐fluoro‐2‐deoxy‐d‐glucose positron emission tomography/computed tomography (FDG‐PET/CT) and bone marrow aspirate and trephine biopsies (BMAT) are used to identify disease involvement.
Imogen Andrews +3 more
wiley +1 more source
Primitive Neuroectodermal Tumor of the Cervix Uteri: A case report and review of literature
International Journal of Hematology-Oncology and Stem Cell Research, 2015 Ewing’s sarcoma is a round cell malignancy of bone and soft tissue that occurs predominately in adolescents and young adults.It is an uncommon malignancy, but is recognized as the second most prevalent primary bone tumor worldwide.
Zineb Benbrahim +5 more
doaj
Organoids in pediatric cancer research
FEBS Letters, EarlyView.Organoid technology has revolutionized cancer research, yet its application in pediatric oncology remains limited. Recent advances have enabled the development of pediatric tumor organoids, offering new insights into disease biology, treatment response, and interactions with the tumor microenvironment.
Carla Ríos Arceo, Jarno Drost
wiley +1 more source