Results 31 to 40 of about 5,957 (165)
Journal of Medical Case Reports, 2023 Background Ewing’s sarcoma is a malignant neoplasm that mainly occurs in skeletal tissue but can rarely arise in soft tissues. Recently, small round cell tumors (including Ewing’s sarcoma) caused by chromosomal translocations have been collectively ...
Kaya Atagi +15 more
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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
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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
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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
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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
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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
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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
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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.
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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
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Pediatric Blood &Cancer, EarlyView.ABSTRACT Background Pediatric sarcomas are a heterogeneous group of tumors that contribute disproportionately to cancer mortality in children. Although congenital anomalies are among the strongest known risk factors for childhood cancer, the risk of specific sarcoma subtypes among affected individuals has not yet been thoroughly evaluated. Procedure We
Russ Wolters +17 more
wiley +1 more source