Results 21 to 30 of about 6,148 (193)
Ewing's sarcoma with distant metastasis: A brief note on management and emerging therapies
Clinics and Practice, 2019 Ewing’s sarcoma is an aggressive fatal malignancy of bones and soft-tissue. It predominantly affects the young population, with a worldwide incidence of three cases per million. The pelvis, extremities, and ribs are the most common sites.
Girish Gulab Meshram +2 more
doaj +1 more source
Subungual Ewing sarcoma/PNET tumor family of the great toe: a case report
Electronic Physician, 2016 Ewing's sarcoma is seen mainly in patients less than 18. This aggressive tumor generally affects the axial skeleton and only rarely involves the acral regions. Ewing’s sarcoma in the foot is inordinately scarce.
Fariba Binesh +3 more
doaj +1 more source
Sinonasal Ewing's sarcoma: Recognition and management of a rare disease
Otolaryngology Case Reports, 2021 Nasal mass in the pediatric population is most commonly benign and thus treated with low suspicion for malignancy. Ewing's sarcoma is the most common pediatric malignancy and usually arises in the diaphysis of long bones.
Zachary D. Urdang +2 more
doaj +1 more source
Ewing’s sarcoma of the right kidney with multiple metastasis on PET/CT
The Egyptian Journal of Radiology and Nuclear Medicine, 2023 Background Ewing’s sarcoma is categorized as small round cell aggressive tumor which commonly occurs in bone and soft tissue. Primary renal Ewing’s sarcoma is an extremely rare entity and accounts for less than 1% of renal masses.
Man Mohan Singh +4 more
doaj +1 more source
The role of imaging in the evaluation of extraskeletal Ewing’s sarcoma
South African Journal of Radiology, 2013 Primary bone tumours account for 5% of all adolescent and child cancers. When Ewing’s sarcoma arises in soft tissue rather than bone, it is referred to as extraskeletal Ewing’s sarcoma (ESS).
Pieter Barnardt, Francois Roux
doaj +1 more source
Discovery and Validation of a Compound to Target Ewing’s Sarcoma
Pharmaceutics, 2021 Ewing’s sarcoma, characterized by pathognomonic t (11; 22) (q24; q12) and related chromosomal ETS family translocations, is a rare aggressive cancer of bone and soft tissue.
Ellie Esfandiari Nazzaro +9 more
doaj +1 more source
CA: A Cancer Journal for Clinicians, 1976 There are no known external causes of Ewing’ sarcoma, a form of bone cancer, although a small number of cases are linked to genetic abnormalities. This malignancy occurs with remarkable consistency in registry populations across Europe and the United States, including Los Angeles County. Few cases of it occur after age 30.
openaire +3 more sources
Ewing's sarcoma of the calcaneum
Indian Journal of Medical and Paediatric Oncology, 2017 Ewing's sarcoma of the calcaneum is rare. Radiological features of this tumor can be misinterpreted as other benign bone tumors due to its rarity. The overall prognosis of Ewing's sarcoma of calcaneum is inferior compared to other sites of this tumor.
Sherif, P Ajmal, Santa, A
openaire +2 more sources
Personalized Zebrafish Models for Fusion‐Positive Pediatric Sarcomas
Pediatric Blood &Cancer, EarlyView.ABSTRACT Clinical sequencing efforts have revolutionized our approaches to categorizing pediatric cancers in real time. This has dramatically improved our ability to profile pediatric tumors, identify actionable vulnerabilities, and influence clinical care.
Lisa H. Hall +2 more
wiley +1 more source
Silent Malignant Occipital Swelling
Medical Journal of Dr. D.Y. Patil Vidyapeeth, 2018 Ewing's sarcoma commonly reported in long bones and pelvis. Primary Ewing's sarcoma of the cranium is rare. They behave differently from their counterpart involving the long bones. They usually respond well to chemotherapy and radiotherapy.
Sumeet V Sasane +4 more
doaj +1 more source