Results 81 to 90 of about 10,925 (230)
Limb Salvage for Malignant Bone Tumors in Young Children [PDF]
, 2000 From March 1984 to April 1991, the Orthopaedics Department of the Clínica Universitaria de Navarra treated 47 cases of malignant bone tumors in young children by limb-salvage surgery. Mean follow-up time was 4.4 years.
Cara, J.A. (José Antonio) +1 more
core
Intercalary bone allografts 23 tumor cases followed for 3 years [PDF]
, 1994 From 1987 to 1991, 26 patients with malignant bone tumors (osteosarcoma, Ewing's sarcoma, chondrosarcoma and malignant fibrous histiocytoma) in the diaphysis or metaphysis of long bones have been treated by chemotherapy, radiotherapy and intercalary bone
Cara, J.A. (José Antonio) +2 more
core +1 more source
Primary bronchial Ewing sarcoma
International Journal of Surgery Case Reports, 2019 Primary bronchial Ewing sarcoma (ES) is a rare endobronchial tumor.A 65-year-old male presented with six-month history of progressive shortness of breath. Flexible bronchoscopy showed an endobronchial polypoid tumor in the left main stem bronchus about 2 cm from the carina.
Hamid Mumtaz +4 more
openaire +2 more sources
Clinicopathologic Analysis of Sarcomas in the Oral and Maxillofacial Region: A Systematic Review
Oral Diseases, EarlyView.ABSTRACT Objective This study aimed to systematically review primary sarcomas in the oral and maxillofacial region, focusing on patient demographics and sarcoma‐specific characteristics, including clinical presentation, histopathology, treatment approaches, outcomes, and survival rates.
Iara Vieira Ferreira +7 more
wiley +1 more source
Congenital Ewing’s Sarcoma, a Rare and Difficult Diagnosis: A Case Report
Eurasian Journal of Medicine, 2019 We have interestedly read the article written by Thalia Wong BS in July 2015, which is about Pediatric Blood Cancer, including clinical findings and results of infants
Gulsah Aynaoglu Yildiz +3 more
doaj +1 more source
Photochemistry and Photobiology, EarlyView.Exposure to solar ultraviolet radiation is the main etiologic driver of nonmelanoma skin cancers (NMSCs), including basal cell (BCC) and cutaneous squamous cell carcinomas (cSCC), which are the most prevalent types of cancers in the US. In this study, we demonstrate that the serine/threonine kinase Polo‐like kinase 4 (PLK4) is overexpressed in NMSCs ...
Mary A. Ndiaye +5 more
wiley +1 more source
Cyclin D1 as a Useful Marker for the Differentiation of Ewing’s Sarcoma from Rhabdomyosarcoma
Middle East Journal of Cancer, 2020 Background: The main oncogenic action of CD99 and cyclin D1 biomarkers is referred to any mutation, amplification, and overexpression in cyclin D1 coding gene, altering cell cycle progression as the main mechanism observed in a variety of tumors.
Tina Shooshtarizadeh +2 more
doaj +1 more source
Ewing Family Tumors: Potential Prognostic Value of Reverse-Transcriptase Polymerase Chain Reaction Detection of Minimal Residual Disease in Peripheral Blood Samples [PDF]
, 1998 In more than 95% of patients, the Ewing family of tumors (ET) has chimeric transcripts caused by fusion of the EWS gene to either FLI1 or ERG. The presence of specific EWS-FLI1 or EWS-ERG transcripts in peripheral blood (PB) samples of
Alava, E. (Enrique) de +4 more
core
Sclerosing epithelioid fibrosarcoma as a rare cause of ascites in a young man: a case report [PDF]
, 2008 Introduction Sclerosing epithelioid fibrosarcoma is a rare but distinct variant of fibrosarcoma that not only presents as a deep-seated mass on the limbs and neck but can also occur adjacent to the fascia or peritoneum, as well as the trunk and spine. We
Philip J Smith +11 more
core +2 more sources
Downstream EWS/FLI1 - upstream Ewing's sarcoma [PDF]
Genome Medicine, 2010 Ewing's sarcoma family tumors are a good example of how genome research has advanced our understanding of the molecular pathogenesis of an otherwise enigmatic disease. This group of embryonal bone tumors is characterized by the expression of a chimeric ETS-family oncogene, predominantly EWS/FLI1.
openaire +2 more sources