Results 91 to 100 of about 7,674 (209)
Rare childhood tumors in a Turkish pediatric oncology center
Background: It has been estimated that rare tumor rate is about 15% of all childhood cancer in United States. According to Turkish Pediatric Oncology Group (TPOG) datas, 8889 children were diagnosed between 2002 and 2008 in our country and 3.7% of them ...
Nurdan Tacyildiz +9 more
doaj +1 more source
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
Significance of immunohistochemistry in accurate characterization of malignant tumors [PDF]
Background: To determine in a large series of surgical biopsies the role and significance of immunohistochemistry in the adequate and accurate characterization of malignant tumors.
Ahmed, Rashida +6 more
core +1 more source
Primary Ewing’s sarcoma of the intestine: case report and literature review
Ewing sarcoma (ES)/peripheral primitive neuroectodermal tumor is a highly aggressive malignant tumor that typically presents in bone and soft tissue. Primary ES of the intestine is relatively rare, which poses a challenge in distinguishing it from other ...
Baofa Luo +4 more
doaj +1 more source
No improvement of survival with reduced- versus high-intensity conditioning for allogeneic stem cell transplants in Ewing tumor patients [PDF]
Background: Outcomes of Ewing tumor (ET) patients treated with allogeneic stem cell transplantation (allo-SCT) were compared regarding the use of reduced-intensity conditioning (RIC) and high-intensity conditioning (HIC) regimens as well as human ...
Abdel-Rahman, F. +60 more
core
Background Intracranial primitive neuroectodermal tumors (PNETs) are characterized by poorly differentiated, highly malignant, aggressive small round tumor cells originating from the central and peripheral nervous systems. Case presentation A 25-year-old
Dejing Cheng +3 more
doaj +1 more source
Association of EWS-FLI1 Type 1 Fusion with Lower Proliferative Rate in Ewing’s Sarcoma [PDF]
The Ewing's sarcoma (ES) family of tumors, including peripheral neuroectodermal tumor (PNET), is defined genetically by specific chromosomal translocations resulting in fusion of the EWS gene with a member of the ETS family of ...
Alava, E. (Enrique) de +6 more
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Intracranial peripheral-type primitive neuroectodermal tumor.
A 15-year-old man presented with headache. Magnetic resonance (MR) imaging revealed a large extraaxial tumor with cyst at the right frontotemporal region. The solid part of the tumor was homogeneously enhanced on T(1)-weighted MR imaging after injection of gadolinium.
Yuichi, Furuno +6 more
openaire +1 more source
Peripheral Primitive Neuroectodermal Tumor of Breast.
Peripheral primitive neuroectodermal tumor (PNET) is a malignant tumor of the young, usually found in bony structures. It is extremely rare to find it in the breast. Only 9 cases have been reported in the medical literature. A35-year lady had a painless lump in upper left outer quadrant of her left breast which appeared as a BIRADS III lesion on ...
Khalid Hamid, Changal +3 more
openaire +1 more source
Molecular and immunohistochemical characterisation of matched primary and metastatic Ewing sarcomas
Die Diagnostik von Ewing-Sarkomen (ES) basiert auf molekularpathologischen und immunhistochemischen Analysen. In einer früheren Arbeit wurde ein Patient mit zwei separaten ES beschrieben, in denen unterschiedliche EWSR1-Translokationen nachgewiesen ...
Wentker, D. (Dennis)
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