Results 21 to 30 of about 14,338 (204)

Pre-B-cell acute lymphoblastic leukemia with bulk extramedullary disease and chromosome 22 (EWSR1) rearrangement masquerading as Ewing sarcoma [PDF]

open access: yes, 2010
We report a 2-year-old female with a subcutaneous tumor who was initially misdiagnosed as suffering from Ewing sarcoma with a positive EWSR1 rearrangement and EWS/FLI1 transcript.
Jakovljević, Gordana   +6 more
core   +1 more source

A rare case of a peripheral Ewing sarcoma primitive neuroectodermal tumor of pelvic origin

open access: yesRadiology Case Reports, 2023
Primitive neuroectodermal tumors (PNET) represent malignant neuroectodermal tumors composed of small round cells. They can be differentiated between originating from the peripheral nervous system or the central nervous system. Peripheral PNET (pPNET) can
Erinie Mekheal, MD   +5 more
doaj   +1 more source

Therapeutic approach in glioblastoma multiforme with primitive neuroectodermal tumor components: case report and review of the literature [PDF]

open access: yes, 2018
Glioblastoma multiforme (GBM) is the most common and aggressive malignant glioma that is treated with first-line therapy, using surgical resection followed by local radiotherapy and concomitant/adjuvant temozolomide (TMZ) treatment.
Berrios J. R. G.   +12 more
core   +1 more source

Uterine primitive neuroectodermal tumor with adenosarcoma: a case report

open access: yesJournal of Medical Case Reports, 2010
Introduction Primitive neuroectodermal tumor of the uterus is extremely rare. They occur as either pure primitive neuroectodermal tumors or admixed with neoplasms of mullerian origin.
Chawla Indu   +3 more
doaj   +1 more source

Cervical Primitive Neuroectodermal Tumor in an Adult: Case Report and Literature Review*

open access: yesBrazilian Neurosurgery, 2022
Introduction Primitive neuroectodermal tumors are rare neoplasms of the central nervous system that occur in children, with few reports in adults. These tumors are found most often in the cerebral hemispheres, with spinal cord disorders being rare.
Guilherme dos Santos de Alencar   +7 more
doaj   +1 more source

Peripheral primitive neuroectodermal tumour - A rare cause of a popliteal fossa mass: A case report and review of the literature [PDF]

open access: yes, 2014
A literature review of peripheral primitive neuroectodermal tumours, illustrated with an index case report describing an 80-year-old woman who presented with a mass in the left popliteal fossa, is reported.
Choong, Andrew M. T. L.   +5 more
core   +1 more source

Primitive neuroectodermal tumor of the kidney in a young male: Case report and review of literature

open access: yesUrology Annals, 2015
Primitive neuroectodermal tumor of the kidney is a rare tumor. A total of approximately 79 primary renal cases have been reported to date. Primitive neuroectodermal tumors occur preferentially in the soft-tissues of the paravertebral region and chest ...
Nivedita Patnaik   +3 more
doaj   +1 more source

Supratentorial primitive neuroectodermal tumor in an adult: a case report and review of the literature

open access: yesJournal of Medical Case Reports, 2012
Introduction Supratentorial primitive neuroectodermal tumors predominantly occur in children, and are rare in the adult population. Less than 100 cases of supratentorial primitive neuroectodermal tumor have been reported in adults internationally.
Lawandy Shokry   +6 more
doaj   +1 more source

Surgical treatment of retrosternal extraosseous Ewing Sarcoma in a 6-years old female: a clamshell approach with hemysternectomy and application of a non-crosslinked extracellular matrix [PDF]

open access: yes, 2017
Background Ewing Sarcoma (ES) and Neuroblastoma (NB) belong to a family of tumours of primitive neuroectodermal origin (PNET) that occurs in both bone and soft tissue. Notwithstanding ES and NB are two distinct malignant tumours, sometimes there could be
Angotti, Rossella   +9 more
core   +3 more sources

Molecular features in a biphenotypic small cell sarcoma with neuroectodermal and muscle differentiation [PDF]

open access: yes, 1998
We report a case of a 13-year-old girl with soft tissue sarcoma of the hand, which showed muscle and neuroectodermal immunophenotypes. Molecular studies were performed on RNA collected from fine-needle aspiration (FNA) cytology and ...
Alava, E. (Enrique) de   +8 more
core   +1 more source

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