Results 31 to 40 of about 5,409 (178)
Outcome of multidisciplinary treatment of peripheral primitive neuroectodermal tumor [PDF]
AbstractPeripheral primitive neuroectodermal tumors (PNETs) constitute very rare and aggressive malignancies. To date, there are no standard guidelines for management of peripheral PNETs due to the paucity of cases arising in various body sites. Therapeutic approach is derived from Ewing sarcoma family, which currently remains multimodal.
Yidi Liu +10 more
openaire +2 more sources
Ewing′s sarcomas and peripheral primitive neuroectodermal tumors (ES/PNETs) are high grade malignant neoplasms. These malignancies are characterized by a chromosome 22 rearrangement, arise from bone or soft tissue, predominantly affect children and young
Alessia Reali +6 more
doaj +1 more source
Radiological and pathological diagnosis of an incidental Askin tumor
A 53-year-old male with no significant past medical history presented with an acute traumatic fracture of his thumb. Preoperative chest radiograph before K-wire fixation demonstrated an incidental 9 cm opacity of the left lung.
Brian Covello, MD +3 more
doaj +1 more source
ABSTRACT Pediatric cancer is a significant cause of morbidity and mortality in children. The etiologies of pediatric cancer are largely unknown, but environmental pesticide exposures are likely to contribute. Chronic low‐dose exposure to pesticide mixtures through drinking water is a growing concern in agricultural communities.
Grace N. VanDeSteeg +4 more
wiley +1 more source
Peripheral primitive neuroectodermal tumor of the cervical spine
Primitive neuroectodermal tumor (PNET) is a malignant neoplasm that generally arises from bone and soft tissues, with predilection for young adults. This neural crest origin tumors share biologic and histologic features with Ewing's sarcoma (ES).We present a case of a 22-year-old woman with history of severe progressive neck pain, without radiation ...
Cabral, Gustavo A. P. S. +10 more
openaire +3 more sources
ABSTRACT Ewing sarcoma and primitive neuroectodermal tumors share histological and genetic characteristics, yet differ in management, with EWSR1 rearrangement being the key distinguishing factor. Such intracranial tumors lacking this rearrangement are rare in adults.
Shubham Dokania +7 more
wiley +1 more source
Peripheral primitive neuroectodermal tumors (PNET) are rare malignant tumors, affecting mostly children and adolescents and have been described in breast in eight case reports only.
N. Majid +7 more
doaj +1 more source
Primitive neuroectodermal tumors (PNET) are highly malignant, yet relatively uncommon neoplasms of the central nervous system. Although a host of different parts of the nervous system can be affected, intramedullary location of PNET is extremely rare ...
Pradeep Sharma +9 more
doaj +1 more source
Skull Base Surgery in the Pediatric Population—The 2nd International Collaborative Study (1995–2015)
ABSTRACT Background The current study presents the efforts of a global collaborative group to review the management and outcomes of malignant tumors of the skull base in the pediatric population worldwide. Patients and Methods A total of 28 institutions contributed data on 3061 patients. From this, there were 64 pediatric patients (2.1%).
Dan M. Fliss +50 more
wiley +1 more source
The Role of N6‐Methyladenosine Modification in Health and Disease
N6‐methyladenosine (m6A) is the most prevalent internal RNA modification in eukaryotes, acting as a pivotal epitranscriptomic regulator of RNA metabolism. This modification plays a dual role: it maintains physiological homeostasis under normal conditions but drives disease progression when dysregulated.
Linghuan Li +6 more
wiley +1 more source

