Results 11 to 20 of about 12,013 (184)

Peripheral Primitive Neuroectodermal Tumor of the Pelvis [PDF]

open access: yesIranian Journal of Medical Sciences, 2014
The primitive neuroectodermal tumor (PNET) belongs to a group of highly malignant tumors and is composed of small round cells of a neuroectodermal origin.
Zohreh Yousefi   +4 more
doaj   +3 more sources

Peripheral primitive neuroectodermal tumor of the orbit in Graves' ophthalmopathy - A rare presentation. [PDF]

open access: yesSaudi J Ophthalmol, 2023
Graves' ophthalmopathy is the most common cause of both unilateral and bilateral proptoses in adults. Peripheral primitive neuroectodermal tumor (pPNET) is a small round cell malignant lesion of neuroectodermal origin which very rarely affects the orbit.
Stephen MA   +3 more
europepmc   +2 more sources

Intracranial peripheral primitive neuroectodermal tumor presenting as neurosurgical emergency: A report of two cases. [PDF]

open access: yesJ Neurosci Rural Pract, 2023
Ewing’s sarcoma/peripheral primitive neuroectodermal tumor (ES/pPNET) belongs to the family of malignant small and blue round cell tumors. It usually occurs in children and young adults with 3/4th of the cases arising from bone and 1/4 from soft tissue ...
Datta D   +4 more
europepmc   +2 more sources

The prognostic factors of Ewing sarcoma/peripheral primitive neuroectodermal tumor: A retrospective analysis of 67 patients at a single center. [PDF]

open access: yesMedicine (Baltimore), 2022
To investigate the characteristics and factors that impact the prognosis of Ewing sarcoma/peripheral primitive neuroectodermal tumor (ES/pPNET) patients.
Peng J, Han XM.
europepmc   +2 more sources

Congenital Ewing's Sarcoma/Peripheral Primitive Neuroectodermal Tumor: A Case Report and Review of the Literature

open access: yesPediatrics and Neonatology, 2016
Ewing's sarcoma (EWS) and peripheral primitive neuroectodermal tumor (pPNET) are small round cell malignancies that develop in soft tissue and bone. They very rarely affect newborns.
Shu-Guang Jin   +2 more
doaj   +4 more sources

Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor and Related Tumors [PDF]

open access: yesPediatric and Developmental Pathology, 2012
Ewing sarcoma/peripheral primitive neuroectodermal tumor (EWS/pPNET) and other tumors with EWS gene rearrangements encompass a malignant and intermediate neoplasm with a broad anatomic distribution and a wide age range but a predilection for soft tissue in children, adolescents, and young adults.
Maria Tsokos   +2 more
exaly   +6 more sources

Primary intradural extramedullary extraosseous Ewing's sarcoma/peripheral primitive neuroectodermal tumor (PIEES/PNET) of the thoracolumbar spine: A case report and literature review. [PDF]

open access: yesOpen Med (Wars), 2021
We present a rare case of a primary intradural extramedullary Ewing’s sarcoma/peripheral primitive neuroectodermal tumor (PIEES/PNET) in the thoracolumbar spine and review the current literature.
Pu F, Liu J, Zhang Z, Guo T, Shao Z.
europepmc   +2 more sources

Primary intracranial peripheral primitive neuroectodermal tumor in an adult patient with aphasia: A rare case report. [PDF]

open access: yesClin Case Rep, 2022
Primary intracranial peripheral primitive neuroectodermal tumors (pPNETs) are extremely rare malignancies that commonly affect children and adolescents. Only 10 cases over the age of 33 have been reported.
Ghaemi K   +2 more
europepmc   +2 more sources

Primary intracranial peripheral primitive neuroectodermal tumor: lessons from an exceptionally rare neoplasm. Illustrative case. [PDF]

open access: yesJ Neurosurg Case Lessons
BACKGROUND The primary intracranial peripheral primitive neuroectodermal tumor (pPNET) is a lesion subtype within the Ewing sarcoma family of tumors. pPNETs are extremely uncommon pathologies, accounting for 0.03% of intracranial tumors and 1% to 2% of ...
Bocanegra-Becerra JE   +4 more
europepmc   +2 more sources

Isolated cardiac peripheral primitive neuroectodermal tumor: A case report [PDF]

open access: yesCancer Biology and Therapy, 2017
Jinfu Yang   +2 more
exaly   +3 more sources

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