Results 61 to 70 of about 30,215 (266)
Brainstem Neuroectodermal Tumors
Seven histologically confirmed primitive neuroectodermal tumors (PNETs) arising in the brainstem were identified among 146 pediatric brainstem tumors, in a review of the the clinical neuro-oncology database and 1986-1995 files of the Division of ...
J Gordon Millichap
doaj +1 more source
Anticancer Molecular Mechanisms of Curcuminoids: An Updated Review of Clinical Trials
Curcuminoids remain one of the most studied dietary polyphenols as a cancer prevention and treatment agent. Inflammation and tumor progression are related to the NF‐κB signaling pathway, which is also suppressed by curcuminoids. Curcuminoids prevent the activation of a variety of signaling pathways, including the MAPK, PI3K/Akt, and NF‐kB pathways ...
Ushna Momal +14 more
wiley +1 more source
Primitive Neuroectodermal Tumor Prognosis
Biological factors of prognostic significance in primitive neuroectodermal tumors (PNETs) were evaluated in tumor specimens of 86 children examined at the Children’s Hospital of Philadelphia and University of Pennsylvania.
J Gordon Millichap
doaj +1 more source
Systemic treatment of malignant gastrointestinal neuroectodermal tumour after childhood neuroblastoma: chemotherapy in malignant gastrointestinal neuroectodermal tumour [PDF]
Malignant gastrointestinal neuroectodermal tumour is an extremely rare neoplasm that arises in the wall of the small bowel, stomach or large bowel in youngaged and middle-aged adults.
D'Alessandro, V. +12 more
core +1 more source
We present a case of a 42‐year‐old woman presenting with pleural effusion, a rare manifestation of Ewing sarcoma. ABSTRACT Extraskeletal Ewing sarcoma (EES) is a rare malignant tumour within the “Ewing family of tumours,” first described by Tefft et al. in 1969.
Hamza Khan Khattak +6 more
wiley +1 more source
Chemotherapy For Medulloblastoma
The efficacy of adjuvant chemotherapy for patients with poor-risk medulloblastoma/primitive neuroectodermal tumors (MB/PNET) has been studied at the Children’s Hospital of Philadelphia, University of Pennsylvania, PA.
J Gordon Millichap
doaj +1 more source
Primitive neuroectodermal tumor of the kidney: an experience of three cases
Background Primitive neuroectodermal tumors (PNET) are highly aggressive tumors belonging to the Ewing’s sarcoma family. Primitive neuroectodermal tumor is a group of bone and soft tissue tumor arising from neuroectodermal tissues. They are characterized
Ankitkumar Sharma +4 more
doaj +1 more source
Diffusion, Perfusion, and Histopathologic Characteristics of Desmoplastic Infantile Ganglioglioma. [PDF]
We present a case series of a rare tumor, the desmoplastic infantile ganglioglioma (DIG) with MRI diffusion and perfusion imaging quantification as well as histopathologic characterization. Four cases with pathologically-proven DIG had diffusion weighted
Bonnin, Jose +3 more
core +1 more source
Scrotal Peripheral Primitive Neuroectodermal Tumor
The peripheral primitive neuroectodermal tumor (pPNET) is a rare malignant tumor originating from neuroectoderm that usually occurs in children or adolescent and is frequently located in the extremities, chest cavity, pelvic cavity and chest wall. We present a rare case of an 84-year-old man with a history of pPNET in the scrotal sac, to our knowledge ...
Sandra, Baleato-González +3 more
openaire +2 more sources
Neuroectodermal tumor cells, like neural crest (NC) cells, are pluripotent, proliferative, and migratory. We tested the hypothesis that genetic programs essential to NC development are activated in neuroectodermal tumors.
Timothy R. Gershon +3 more
doaj +1 more source

