Results 51 to 60 of about 5,323 (178)
Peripheral primitive neuroectodermal tumor of the pelvis.
The primitive neuroectodermal tumor (PNET) belongs to a group of highly malignant tumors and is composed of small round cells of a neuroectodermal origin. Categorized in the same tumor family as Ewing sarcoma, the PNET is most likely to occur in bones and soft tissues.
Zohreh Yousefi +4 more
openaire +2 more sources
Paravaginal peripheral primitive neuroectodermal tumor: A rare tumor
AbstractPeripheral primitive neuroectodermal tumor (PNET) of the female genital tract, particularly those in the vaginal and paravaginal region, are extremely rare. A 36-year-old woman presented with clinical features similar to that of a case of cervical fibroid.
Samrat Dutta +2 more
openaire +3 more sources
A Peripheral Primitive Neuro-ectodermal Tumor (pPNET) of Larynx
Introduction Primitive neuroectodermal tumors (PNETs) are malignant tumors comprised of small round cells of neuro-ectodermal origin that affect soft tissue and bone.
Raman Wadhera +4 more
doaj
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
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
Peripheral Primitive Neuroectodermal Tumor: A Rare Case in Pediatrics
Primitive neuroectodermal tumors (PNETs) are a type of malignant tumors made up of small neuroectodermal-derived round cells that affect soft tissue and bone, with a wide range of clinical symptoms and histological commonalities depending on the site of the tumor. PNETs account for 4% of all pediatric and adolescent cancers.
Rashed, Atef A +4 more
openaire +2 more sources
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
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
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

