Results 61 to 70 of about 14,338 (204)
Diffuse intrinsic pontine glioma biopsy: A single institution experience [PDF]
, 2014 Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/109626/1/pbc25224 ...
Altinok, Deniz +6 more
core +1 more source
Clinical Case Reports, Volume 14, Issue 1, January 2026.ABSTRACT Chest‐wall Ewing sarcoma (CWES) is uncommon in adults and often abuts vital thoracic structures, making R0 resection challenging despite gains with multimodal therapy. A 46‐year‐old Arab male presented with year‐long right‐sided chest pain, weight loss, and a firm mass over the lower right ribs.
Mohammad Alaa Aldakak +5 more
wiley +1 more source
Chemotherapy For Medulloblastoma
Pediatric Neurology Briefs, 1988 The efficacy of adjuvant chemotherapy for patients with poor-risk medulloblastoma/primitive neuroectodermal tumors (MB/PNET) has been studied at the Children’s Hospital of Philadelphia, University of Pennsylvania, PA.
J Gordon Millichap
doaj +1 more source
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
Primitive neuroectodermal tumor of the central nervous system: report of four cases [PDF]
, 1994 The clinicopathological and immunohistochemical features of four cases of primitive neuroectodermal tumors of the central nervous system were investigated. Three patients died.
Minett, Thaís Soares Cianciarullo +2 more
core +2 more sources
Scrotal Peripheral Primitive Neuroectodermal Tumor
Current Urology, 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 ...
Sandra, Baleato-González +3 more
openaire +2 more sources
Histopathology, Volume 88, Issue 2, Page 503-514, January 2026.Our results support that low grade glial tumours of germ cell origin (LGGTs) represent a phenomenon of maturation (either spontaneous or induced by therapy) of embryonic‐type neuroectoderm, being possibly equivalent to teratoma from a biological perspective.
João Lobo +10 more
wiley +1 more source
Neoplasia: An International Journal for Oncology Research, 2005 Neuroectodermal tumor cells, like neural crest (NC) cells, are pluripotent, proliferative, and migratory. We tested the hypothesis that genetic programs essential to NC development are activated in neuroectodermal tumors.
Timothy R. Gershon +3 more
doaj +1 more source
Diffusion, Perfusion, and Histopathologic Characteristics of Desmoplastic Infantile Ganglioglioma. [PDF]
, 2016 We present a case series of a rare tumor, the desmoplastic infantile ganglioglioma (DIG) with MRI diffusion and perfusion imaging quantification as well as histopathologic characterization. Four cases with pathologically-proven DIG had diffusion weighted
Bonnin, Jose +3 more
core +1 more source
Molecular pathology of testicular germ cell tumours: an update for practicing pathologists
Histopathology, Volume 88, Issue 1, Page 214-229, January 2026.Molecular testing for isochromosome 12p is usually only necessary in difficult cases that encompass metastases or recurrent diseases including somatic‐type malignancies. So far, no breaking progress has been made in the field of targeted therapy as TGCTs only rarely show targetable molecular alterations.
Alexander Fichtner +3 more
wiley +1 more source