Results 51 to 60 of about 5,409 (178)
FOXM1 is an oncogenic mediator in Ewing Sarcoma. [PDF]
Ewing Family Tumors (Ewing Sarcoma and peripheral Primitive Neuroectodermal Tumor) are common bone and soft tissue malignancies of childhood, adolescence and young adulthood.
Laura Christensen +5 more
doaj +1 more source
Primitive neuroectodermal tumor of prostate
Primitive neuroectodermal tumors (PNETs) are malignant proliferations of small, undifferentiated neuroectodermal cells occurring mainly in children and share the same reciprocal translocation between chromosomes 11 and 22 and the same patterns of ...
Kumar Vikash +6 more
doaj
Development of the neurohypophysis: A major neuroendocrine interface
Abstract The neurohypophysis is a major central neuroendocrine interface regulating reproductive functions and water homeostasis. Distinct neurovascular cell types interact via evolutionarily conserved signaling molecules in the developing neurohypophysis, providing a model system for studying principles in neuroendocrine interface morphogenesis.
Athul R. Ramesh +5 more
wiley +1 more source
Ewing’s sarcoma/peripheral primitive neuroectodermal tumor is a small, round, and blue cell malignancy that occurs most often in bone and soft tissues of children and young adults.
Sandhya Bordia +3 more
doaj +1 more source
Heterogeneity of extraparenchymal primitive neuroectodermal tumors within the craniospinal axis.
Four cases of primitive neuroectodermal tumors (PNETs) with unusual localization (three intraspinal extramedullary and one pontocerebellar) are reviewed. Histologically, they were small round blue cell tumors with diverse patterns. Immunohistochemically,
M Debiec-Rychter +7 more
doaj +1 more source
Background Primary Ewing sarcoma (ES)/peripheral primitive neuroectodermal tumors (pPNETs) are aggressive bone tumors that rarely occur in the axial skeleton, including the cranial bone and mobile spine.
Jun Chen +6 more
doaj +1 more source
Mediastinal Ewing’s sarcoma is an exceptionally rare malignancy, with an incidence of approximately 0.3%. Due to the rarity of the tumor and challenges such as limited tissue availability, diagnosis can be difficult. Curative treatment typically requires a multimodal approach, including intensive chemotherapy, surgery, and radiation therapy.
Anusha Manje Gowda +2 more
wiley +1 more source
Primitive neuroectodermal tumor is a small round cell malignancy which rarely involves the orbit. We report a case of a two-year old male child presenting as unilateral eccentric proptosis with extraconal and intraconal mass, diagnosed as primary ...
Kim Usha +3 more
doaj
Primary cardiac synovial sarcoma (PCSS) is an exceedingly rare tumor. This study presents a comprehensive analysis of six novel PCSS cases identified within our institutional cohort, compared with published literature cohorts, focusing on their clinical presentations, histopathological features, immunohistochemical and molecular characteristics ...
Yi-Xiang Cai +5 more
wiley +1 more source
Sunitinib malate (Sutent™; Pfizer Inc., New York, N.Y., USA) is a small molecule kinase inhibitor with activity against a number of tyrosine kinase receptors, including vascular endothelial growth factor receptors, stem-cell factor receptor, and platelet-
Tiziana Prochilo +6 more
doaj +1 more source

