Results 11 to 20 of about 8,039 (180)

An unusual biconvex epidural lesion: acutely presenting extraosseous intracranial Ewing’s sarcoma

open access: yesChinese Neurosurgical Journal, 2018
Background Ewing’s sarcoma family of tumors consists of small round cell neoplasms, inclusive of primitive neuroectodermal tumor (PNET), Askin’s tumor, and PNET of the bone.
Kalimullah Jan   +2 more
doaj   +2 more sources

Ewing’s sarcoma of ilium, a diagnostic dilemma - case report with review of literature

open access: yesAmerican Journal of Experimental and Clinical Research, 2016
Ewing’s sarcoma is a highly malignant tumor of bone and is more common in children in the age group of 10 to 20 years. Sometimes the classic clinical and radiological presentation of Ewing’s sarcoma may not be the norm and patient may have an atypical ...
Usama Saleh Alshaya   +2 more
doaj   +3 more sources

Ewings Sarcoma Mimicking a Schwannoma: MRI Findings of a Rare Case [PDF]

open access: yesLiaquat National Journal of Cancer Care, 2023
Ewing’s sarcoma is among the most frequent yet highly aggressive neoplasms of the bones presenting in adolescents and children under the age of ten with a slight male predilection. It is now broadly categorized into a set of tumors recognized as Ewing’s
Raisa Altaf   +5 more
doaj   +1 more source

CD200 overexpression on the survival prognosis of Ewing's sarcoma

open access: yesZhongguo linchuang yanjiu, 2023
Objective To explore the role of CD200 in Ewing's sarcoma and its possible pathological mechanisms, and to search for potential drugs that can improve the survival prognosis of Ewing's sarcoma patients.
LIU Zi-rui, LI Jin-feng, LI Yun-long, YANG Hao, ZHAO Liang
doaj   +1 more source

Extra-skeletal Ewing's sarcoma, a rare condition of the submandibular salivary gland, a case report

open access: yesOral and Maxillofacial Surgery Cases, 2022
Extra-skeletal Ewing's sarcoma (ESS) is rarely found in the head and neck region, soft tissue presentation of Ewing's sarcoma is uncommon, morphologically it resembles Ewing's sarcoma originates from bone.
Abdul-Aziz Alaqeeli   +3 more
doaj   +1 more source

Primary Ewing’s sarcoma of sphenoid sinus: A case report and literature review

open access: yesFrontiers in Oncology, 2022
BackgroundPrimary Ewing’s sarcoma of sphenoid sinus, observed in children and adolescents, is an extremely rare malignancy. Such rarity makes the imaging features and treatment strategies for Ewing’s sarcoma of sphenoid sinus unclear. This study aimed to
Kunpeng Wu   +8 more
doaj   +1 more source

Primary pulmonary Ewing’s sarcoma: rare cause of massive hemothorax in a young girl-case report

open access: yesBMC Pediatrics, 2021
Background Ewing’s sarcoma is a common malignant bone tumor in children and young adults. Rarely, extra-skeletal soft tissues and visceral organs can also be the site of origin of Ewing’s sarcoma.
Xuefeng Ling   +4 more
doaj   +1 more source

Primary Ewings sarcoma in liver - A rare case report with review of literature

open access: yesIndian Journal of Pathology and Microbiology, 2021
Ewing's sarcoma family of tumours include both peripheral primitive neuroectodermal tumour (PNET) and Ewing's sarcoma including both intraosseous and extra osseous sites.
Anjali Sharma   +4 more
doaj   +1 more source

Ewing's Sarcoma of the Gastrointestinal Tract—A Case Series

open access: yesAsian Journal of Oncology, 2022
Ewing's sarcoma is a neoplasm of the undifferentiated small round cells, which generally affects the bone and deep soft tissues of children and adolescents. Extraskeletal Ewing's sarcomas are less common than skeletal Ewing's sarcoma with the most common
Prakash Purushothaman   +3 more
doaj   +1 more source

Unusual Presentation of a Primary Ewing’s Sarcoma of the Spine with Paraplegia: A Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2015
Ewing’s sarcoma is a primary malignancy of the bone affecting individuals in the second decade of life. Primary sarcomas of the spine are rare and the occurrence of Primary Ewing’s sarcoma in the spine is very rare.
Karthik Kailash Kannan   +2 more
doaj   +1 more source

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