Results 31 to 40 of about 5,323 (178)
Primary extraosseous intracranial Ewing′s sarcoma: Case report and literature review
Ewing′s sarcoma / peripheral primitive neuroectodermal tumors occur most often in bone and soft tissues of children and young adults. The intracranial manifestation of the disease is rare, and when present, this is often misdiagnosed with other varieties
Krishnangshu Bhanja Choudhury +3 more
doaj +1 more source
Rare Renal Incidentaloma in Pregnancy: An Unusual Primitive Neuroectodermal Tumor Presentation
Peripheral Primitive Neuroectodermal Tumors (PNETs) are rare lesions that arise from outside the central nervous system and normally do not affect the genitourinary system.
Gonzalo Torga, Willis Barrow, Misop Han
doaj +1 more source
Peripheric primitive neuroectodermal tumor (Askin)
The case of preoperative diagnosis of peripheric primitive neuroectodermal tumor (pPNET) of the chest with damage of body sternum in 21-year-old patient is presented in Native literature for the first time. CT and echography data as well as serum tumor-markers level are given.
A. N. Makhson +4 more
openaire +1 more source
Ewing Sarcoma of the Kidney: A Rare Entity
Ewing sarcoma and primitive peripheral neuroectodermal tumor (PNET) are high-grade malignant tumors typically found in children and adolescents. These tumors belong to the family of small round cell tumors and are of neuroectodermal origin. Primary Ewing
Maria Fernanda Arruda Almeida +4 more
doaj +1 more source
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
Ewing's sarcoma (EWS) and peripheral primitive neuroectodermal tumor (pPNET) are small round cell malignancies that develop in soft tissue and bone. They very rarely affect newborns.
Shu-Guang Jin +2 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
Persistent Erythrocytosis in a Dog With a Spinal Sclerosing Paraganglioma
ABSTRACT A 7‐year‐old, male, castrated, mixed‐breed dog presented with right pelvic limb lameness and pain on posturing to defecate that began 1.5 years prior to presentation. Radiographs taken 8 months prior to presentation showed a small lytic lesion of the L6 vertebral body, and CBCs showed a persistently increased hematocrit (HCT) for at least 2 ...
Samuel V. Neal +11 more
wiley +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

