Results 41 to 50 of about 30,215 (266)

A Peripheral Primitive Neuro-ectodermal Tumor (pPNET) of Larynx

open access: yesBengal Journal of Otolaryngology and Head Neck Surgery, 2020
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   +1 more source

Primitive neuroectodermal adrenal gland tumour [PDF]

open access: yes, 2014
Ewing's sarcoma, also called primitive neuroectodermal tumour of the adrenal gland, is extremely rare. Only a few cases have been reported in the literature.
Brian HH Lang   +4 more
core   +1 more source

Primitive neuroectodermal tumor (PNET) of the lung in an adult woman [PDF]

open access: yes, 2014
Primary primitive neuroectodermal tumors (PNETs) are extremely rare in the lung and especially in adult women. We describe a case of PNET of the lung with aggressive behavior in 31-year-old woman.
Jiří Ehrmann   +8 more
core   +2 more sources

Adipocyte-Like Differentiation in a Posttreatment Embryonal Rhabdomyosarcoma. [PDF]

open access: yes, 2015
We describe a 16-year-old boy with rhabdomyosarcoma, consistent with embryonal subtype, of the lower extremity who received systemic neoadjuvant chemotherapy and subsequent excision.
Balitzer, Dana   +2 more
core   +9 more sources

A molecular biology and phase II trial of lapatinib in children with refractory CNS malignancies: a pediatric brain tumor consortium study. [PDF]

open access: yes, 2013
High expression of ERBB2 has been reported in medulloblastoma and ependymoma; EGFR is amplified and over-expressed in brainstem glioma suggesting these proteins as potential therapeutic targets. We conducted a molecular biology (MB) and phase II study to
Blaney, Susan M.   +11 more
core   +1 more source

Tumor classification: molecular analysis meets Aristotle [PDF]

open access: yes, 2004
Background Traditionally, tumors have been classified by their morphologic appearances. Unfortunately, tumors with similar histologic features often follow different clinical courses or respond differently to chemotherapy.
Jules J Berman   +29 more
core   +2 more sources

Comparison of Auto‐Contouring Tools for Delineation of Normal Organs at Risk in Paediatric Patients Undergoing Radiotherapy

open access: yesJournal of Medical Radiation Sciences, EarlyView.
Contouring organs at risk (OARs) manually in paediatric patients undergoing cranial‐spinal radiation therapy (CSI) is a time‐consuming, labour‐intensive task. This study aims to assess the accuracy and clinical acceptability of auto‐contours produced by the Siemens DirectORGANS auto‐contouring software on paediatric patients receiving CSI treatment ...
Isabel Cant   +6 more
wiley   +1 more source

Embryonic Tumor with Abundant Neuroepithelium and True Rosettes (ETANTR): Case Report and Literature Review

open access: yesBrazilian Neurosurgery, 2017
The embryonal tumor with abundant neuropil and true rosettes (ETANTR) is an extremely rare variant of the primitive neuroectodermal tumor (PNET). About 80 cases have been reported since its first description in the literature, in 2000.
Cleciton Braga Tavares   +4 more
doaj   +1 more source

Primitive neuroectodermal tumor of maxilla in a 4-year-old child: A rare case report with update on molecular pathogenesis

open access: yesIndian Journal of Dental Sciences, 2022
Primitive neuroectodermal tumor (PNET) belongs to the class of malignant round cell tumor. PNETs show varying degree of neuroectodermal differentiation.
Pavan Patil   +3 more
doaj   +1 more source

Molecular dissection of the mechanism by which EWS/FLI expression compromises actin cytoskeletal integrity and cell adhesion in Ewing sarcoma. [PDF]

open access: yes, 2014
Ewing sarcoma is the second-most-common bone cancer in children. Driven by an oncogenic chromosomal translocation that results in the expression of an aberrant transcription factor, EWS/FLI, the disease is typically aggressive and micrometastatic upon ...
Beckerle, Mary C   +8 more
core   +1 more source

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