Results 51 to 60 of about 8,438 (194)

Case Report: Intracranial peripheral primitive neuroectodermal tumor - Ewing′s sarcoma of dura with transcalvarial-subgaleal extension: An unusual radiological presentation

open access: yesIndian Journal of Radiology and Imaging, 2009
The occurrence of the intracranial, peripheral, primitive, neuroectodermal tumor, Ewing′s sarcoma (pPNET-ES) of the dura, is very rare. Immunophenotypical as well as genetic analyses play key roles in its diagnosis and differentiation from central PNET ...
Shahina Bano   +2 more
doaj   +1 more source

Presacral medulloepithelioma with peritoneal carcinomatosis in an 11-year-old boy: An extremely rare association

open access: yesRadiology Case Reports, 2021
Medulloepithelioma is a rare and highly malignant tumor of infancy and early childhood, and classified as a primitive neuroectodermal tumor. Considering that most cases occur in the central nervous system, development in atypical sites associated with ...
Gabriel Soares Mendonça, MD   +3 more
doaj   +1 more source

Ewing Family Tumors: Potential Prognostic Value of Reverse-Transcriptase Polymerase Chain Reaction Detection of Minimal Residual Disease in Peripheral Blood Samples [PDF]

open access: yes, 1998
In more than 95% of patients, the Ewing family of tumors (ET) has chimeric transcripts caused by fusion of the EWS gene to either FLI1 or ERG. The presence of specific EWS-FLI1 or EWS-ERG transcripts in peripheral blood (PB) samples of
Alava, E. (Enrique) de   +4 more
core  

Perinatal findings and outcomes in a very rare congenital bulky retroperitoneal Ewing sarcoma: A case report

open access: yesPediatric Hematology Oncology Journal, 2021
Congenital Ewing Sarcoma is extremely rare, with a poor prognosis despite early detection and intensive treatment. The Ewing Sarcoma family of tumors (ESFT) is a group of undifferentiated small round cell sarcomas, that includes Ewing sarcoma (ES) and ...
Irene Aracil Moreno   +7 more
doaj   +1 more source

Contribution of multiparameter flow cytometry immunophenotyping to the diagnostic screening and classification of pediatric cancer [PDF]

open access: yes, 2016
This is an open-access article distributed under the terms of the Creative Commons Attribution License.-- et al.Pediatric cancer is a relatively rare and heterogeneous group of hematological and non-hematological malignancies which require multiple ...
Costa, Elaine S.   +2 more
core   +1 more source

Primitive neuroectodermal tumor of prostate

open access: yesIndian Journal of Pathology and Microbiology, 2008
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  

The impact of recent vincristine on human hematopoietic progenitor cell collection in pediatric patients with central nervous system tumors [PDF]

open access: yes, 2014
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/108370/1/trf12574 ...
Bombery, Melissa   +5 more
core   +1 more source

Extraskeletal Ewing’s sarcoma/peripheral primitive neuroectodermal tumor of the small bowel presenting with gastrointestinal perforation

open access: yesClinical and Experimental Gastroenterology, 2019
Vipul D Yagnik,1 Sushil Dawka21Department of Surgical Gastroenterology, Nishtha surgical hospital and research center, Patan, Gujarat, India; 2Department of surgery, SSR Medical College, Belle Rive, MauritiusAbstract: Extraskeletal Ewing’s sarcoma (
Yagnik VD, Dawka S
doaj  

Congenital extraskeletal Ewing′s sarcoma of chest wall - A rare case report

open access: yesIndian Journal of Pathology and Microbiology, 2011
Congenital extraskeletal Ewing′s sarcoma or peripheral primitive neuroectodermal tumor is an extremely uncommon and invariably fatal tumor. We report a case of extraskeletal congenital Ewing′s sarcoma in a female fetus delivered at 34 weeks of gestation ...
Bhagyalakshmi Atla   +3 more
doaj   +1 more source

Haplótipos de diferentes SNPs no interior do gene EWS em indivíduos afetados e não-afetados pelo sarcoma de Ewing [PDF]

open access: yes, 2012
Ewing’s sarcoma was first described by James Ewing in 1921 and it is the second most common bone tumor in children and young adults. Both chromosomal breakage and translocation occur in this sarcoma.
Silva, Déborah Soares Bispo Santos
core  

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