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The World Health Organization has classified the central nervous system primitive neuroectodermal tumors into five subtypes: neuroblastoma, ganglioneuroblastoma, medulloepithelioma, ependymoblastoma, and not otherwise specified PNET. [1] The last one encompasses the PNETs with varying characteristics that hasn't been well defined yet. [1]
Other names. PNET. Micrograph of an H&E stained section of a peripheral PNET. Specialty. Oncology. Primitive neuroectodermal tumor is a malignant (cancerous) neural crest tumor. [ 1] It is a rare tumor, usually occurring in children and young adults under 25 years of age. The overall 5 year survival rate is about 53%.
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Pancreatic neuroendocrine tumours ( PanNETs, PETs, or PNETs ), often referred to as "islet cell tumours", [ 1][ 2] or "pancreatic endocrine tumours" [ 3][ 4] are neuroendocrine neoplasms that arise from cells of the endocrine ( hormonal) and nervous system within the pancreas . PanNETs are a type of neuroendocrine tumor, representing about one ...
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