Results 1 to 10 of about 8,418 (174)

Peripheral primitive neuroectodermal tumor: a case report [PDF]

open access: yesJournal of Medical Case Reports, 2022
Background Primitive neuroectodermal tumors are extremely rare and highly aggressive malignant small round cell tumors that arise from the primitive nerve cells of the nervous system or outside it.
Alije Keka-Sylaj   +5 more
doaj   +4 more sources

Peripheral Primitive Neuroectodermal Tumor of the Pelvis [PDF]

open access: yesIranian Journal of Medical Sciences, 2014
The primitive neuroectodermal tumor (PNET) belongs to a group of highly malignant tumors and is composed of small round cells of a neuroectodermal origin.
Zohreh Yousefi   +4 more
doaj   +3 more sources

Peripheral primitive neuroectodermal tumor of the urinary bladder in an Arab woman with history of squamous cell carcinoma: a case report [PDF]

open access: yesJournal of Medical Case Reports, 2009
Introduction Peripheral primitive neuroectodermal tumors of the urinary bladder are rare and tend to occur in an older age group than do their counterparts in bones and soft tissue.
Al Meshaan Mohd Khaled   +4 more
doaj   +2 more sources

Primitive neuroectodermal tumor of the cervix: a case report [PDF]

open access: yesJournal of Medical Case Reports, 2011
Introduction Peripheral primitive neuroectodermal tumor of the cervix uteri is extremely rare. Between 1987 and 2010, there were only nine cases reported in the English literature, with considerably different management policies.
Boroujeni Parisa   +3 more
doaj   +3 more sources

Scrotal Peripheral Primitive Neuroectodermal Tumor. [PDF]

open access: yesCurr Urol, 2018
The peripheral primitive neuroectodermal tumor (pPNET) is a rare malignant tumor originating from neuroectoderm that usually occurs in children or adolescent and is frequently located in the extremities, chest cavity, pelvic cavity and chest wall. We present a rare case of an 84-year-old man with a history of pPNET in the scrotal sac, to our knowledge ...
Baleato-González S   +3 more
europepmc   +3 more sources

Congenital Cutaneous Peripheral Primitive Neuroectodermal Tumor (pPNET) of Scalp: Youngest Case So Far

open access: yesJournal of Indian Association of Pediatric Surgeons, 2021
Congenital cutaneous peripheral primitive neuroectodermal tumor (pPNET) is very rare and also very rarely located in scalp. Only two cases of PNET as primary tumor in scalp are reported so far in the literature. Non mutilating surgical excision, combined
Parveen Kumar   +3 more
doaj   +2 more sources

Paravaginal peripheral primitive neuroectodermal tumor: A rare tumor

open access: yesIndian Journal of Medical and Paediatric Oncology, 2011
Peripheral primitive neuroectodermal tumor (PNET) of the female genital tract, particularly those in the vaginal and paravaginal region, are extremely rare.
Samrat Dutta   +2 more
doaj   +3 more sources

Primary pulmonary Ewing sarcoma/peripheral primitive neuroectodermal tumor. [PDF]

open access: yesProc (Bayl Univ Med Cent), 2020
Ewing sarcoma/peripheral primitive neuroectodermal tumor (ES/pPNET) is a malignant small round cell sarcoma commonly occurring among children, adolescents, and adults. We report a rare case of ES/pPNET arising from the lung in a 49-year-old woman. She was found to have a mass in the right lung on a screening imaging study for her BRCA2 mutation.
Sohn AJ, Lang B, McCarroll M, Agarwal A.
europepmc   +4 more sources

Primary ovarian peripheral primitive neuroectodermal tumor presented with breast metastasis; Case report [PDF]

open access: yesRare Tumors
Ewing sarcoma family tumors (ESFT) pose diagnostic challenges, which largely depend on the primary site of involvement and tumor stage. Despite advancements in treatment, metastatic ESFTs remain associated with poor outcomes.
Razan Rabi   +2 more
doaj   +2 more sources

Multimodal Treatment of a Peripheral Primitive Neuroectodermal Tumor Originating From the Thoracic Cavity in a Dog [PDF]

open access: yesJournal of Veterinary Internal Medicine
Peripheral primitive neuroectodermal tumor (pPNET) is a very rare, highly malignant tumor encountered in young dogs, with only four necropsy cases in the veterinary literature.
Leah H. Ackerman   +18 more
doaj   +2 more sources

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