Results 81 to 90 of about 8,039 (180)
ABSTRACT Ewing sarcoma and primitive neuroectodermal tumors share histological and genetic characteristics, yet differ in management, with EWSR1 rearrangement being the key distinguishing factor. Such intracranial tumors lacking this rearrangement are rare in adults.
Shubham Dokania +7 more
wiley +1 more source
Extra-skeletal Ewing’s Sarcoma of Caecum Causing Intussusception: First such Reported Case [PDF]
Introduction: Ewing’s sarcoma is a tumor of primitive cells which primarily affects long bones. Extra-skeletal Ewing’s sarcoma has been rarely reported in small bowel.
Aggarwal, Aakanksha +3 more
core
Ewing’s sarcoma is a highly malignant bone tumor commonly affecting diaphysis of long bones & pelvic bones. It belongs to a spectrum of neoplastic disease known as the Ewing sarcoma family of tumors (EFT) that have the same histologic ...
Sameer Yahya, Farah +3 more
core +1 more source
Preclinical models for sarcoma that preserve tumour biology are urgently needed to advance mechanistic understanding and functional precision oncology. 29 early‐passage patient‐derived sarcoma cell (PDC) cultures from 19 patients, representing 11 sarcoma subtypes were established and extensively characterized.
Stefanie Gijsels +19 more
wiley +1 more source
Ewing's sarcoma can affect any bone. Primary localization in the coracoid process is extremely rare and atypical. In the literature there have been a few reports of Ewing's sarcoma of the scapula.
N. Bahlouli +9 more
doaj +1 more source
ABSTRACT CRISPR‐Cas9 genome‐wide screening has been instrumental towards identifying novel targets for drug discovery in cancer research. However, much of this research has centred specifically on adult cancers, with paediatric cancers being underserviced by current research and screening.
Steven He +2 more
wiley +1 more source
Behind the scenes: how the EMILIN/Multimerin family shapes the cancer landscape
The EMILIN/Multimerin family members regulate key hallmarks of cancer—including apoptosis, angiogenesis, metastasis, and tumor microenvironment remodeling. As indicated, their function in immune evasion, drug resistance, and metabolic reprogramming remains largely unexplored.
Evelina Poletto +9 more
wiley +1 more source
Ewing’s Sarcoma of the Adrenal Gland; A Rare Extraosseous Presentation
Ewing sarcoma also known as peripheral primitive neuroectodermal tumors (ES/PPNETs) usually produce in the chest wall, extraosseous soft tissues, and long or flat bones, however only rarely in solid organs.
Uzma Panhwer
core +1 more source
A Case Report: Calcaneal Ewing’s Sarcoma
Introduction: Ewing sarcoma of bone represents the second most common primary malignant tumor of the bone in children and adolescents. The most common primary bony sites include the long bones, pelvis, chest wall, and spine.
Mohammad Zarei +3 more
core +1 more source
Disseminated Intracranial Ewing’s Sarcoma in an Adult:A Rare and Difficult Diagnosis [PDF]
The Ewing sarcoma family of tumors comprises a rare class of cancers of mesenchymal origin. Cases of Ewing’s sarcoma in the central nervous system – specifically, intracranial Ewing’s – are extremely rare.
Katherine B. Peters +5 more
core +1 more source

