Results 61 to 70 of about 12,071 (222)
Primitive neuroectodermal tumor of the kidney: an experience of three cases
African Journal of Urology, 2022 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
A Population‐Based Assessment of Cancer Risk in Children With VACTERL
American Journal of Medical Genetics Part A, Volume 200, Issue 5, Page 1004-1011, May 2026.ABSTRACT Cancer risk in children with VACTERL, a nonrandom co‐occurrence of ≥ 3 defects (vertebral, anal, cardiac, tracheoesophogeal fistula, renal, and limb), remains unclear. We evaluated this association in a population‐based study. We analyzed data from the Genetic Overlap Between Anomalies and Cancer in Kids (GOBACK) Study, a US registry linkage ...
Ji Yun Tark +15 more
wiley +1 more source
A Systematic Review on the Role of Postoperative Radiotherapy in Pelvic Ewing Sarcoma
Cancer Medicine, Volume 15, Issue 5, May 2026.ABSTRACT Ewing Sarcoma of the pelvis has poorer outcomes than other anatomical sites, with complex anatomy often precluding resection with wide margins. The role of postoperative radiotherapy (RT) in improving outcomes remains undefined. A systematic review using Medline, Embase and Cochrane databases (1972–April 2024) evaluated postoperative RT's ...
Angela Hong +16 more
wiley +1 more source
Conservative multimodal management of a primitive neuroectodermal tumor of the thyroid
Rare Tumors, 2013 Primitive neuroectodermal tumors (PNET) represent 1% of sarcomas. Head and neck peripheral PNETs have an intermediate prognosis between abdominopelvic disease and extremities.
Juliette Haudebourg +9 more
doaj +1 more source
Aggressive Desmoplastic Small Round Cell Tumor in an Adult: A Case Report and Literature Review
Clinical Case Reports, Volume 14, Issue 5, May 2026.ABSTRACT Desmoplastic small round cell tumor (DSRCT) is a rare and highly aggressive sarcoma that predominantly affects adolescents and young adults. It is defined by a characteristic chromosomal translocation, t(11;22) (p13;q12), resulting in the EWS–WT1 fusion gene.
Seyed Amir Aledavood +4 more
wiley +1 more source
Clinical Case Reports, 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.
Kazem Ghaemi +2 more
doaj +1 more source
Clinical and Translational Medicine, Volume 16, Issue 5, May 2026.Oncolytic adenoviruses synergise with chemotherapy, radiotherapy and immunotherapy to enhance anti‐tumour efficacy. Chemotherapy and radiotherapy increase tumour susceptibility and antigen release through DNA damage, while immunotherapy restores T‐cell activity.
Vlad Iova +4 more
wiley +1 more source
Extraneural Supratentorial Primitive Neuroectodermal Tumor Metastasis: An Adult Case Report
Indian Journal of Neurosurgery, 2017 Extraneural metastases of supratentorial primitive neuroectodermal tumors (PNET) are very rare and have been reported in only sporadic cases. We present a patient with supratentorial PNET metastasizing to the lung, diagnosed 4 months after cerebral ...
Nidhal Matar +4 more
doaj +1 more source
Pediatric Blood &Cancer, Volume 73, Issue 4, April 2026.ABSTRACT Surveillance imaging aims to detect tumour relapse before symptoms develop, but it's unclear whether earlier detection of relapse leads to better outcomes in children and young people (CYP) with medulloblastoma and ependymoma. This systematic review aims to identify relevant literature to determine the efficacy of surveillance magnetic ...
Lucy Shepherd +3 more
wiley +1 more source