Primitive neuroectodermal tumor
<templatestyles src="Module:Hatnote/styles.css"></templatestyles>
| Primitive neuroectodermal tumor | |
|---|---|
| File:PNET Histopathology HE 200x.jpg
Micrograph of an H&E stained section of a peripheral PNET.
|
|
| Classification and external resources | |
| Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
| ICD-O | M9473/3 |
| DiseasesDB | 31470 |
| eMedicine | ped/2589 neuro/326 |
| Patient UK | Primitive neuroectodermal tumor |
| MeSH | D018242 |
Primitive neuroectodermal tumor (PNET) 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%.[2]
It gets its name because the majority of the cells in the tumor are derived from neuroectoderm, but have not developed and differentiated in the way a normal neuron would, and so the cells appear "primitive".
PNET belongs to the Ewing family of tumors.
Classification
It is classified into two types, based on location in the body: peripheral PNET and CNS PNET.
Peripheral PNET
The peripheral PNET (pPNET) is now thought to be virtually identical to Ewing sarcoma:
"Current evidence indicates that both Ewing's sarcoma and PNET have a similar neural phenotype and, because they share an identical chromosome translocation, they should be viewed as the same tumor, differing only in their degree of neural differentiation. Tumors that demonstrate neural differentiation by light microscopy, immunohistochemistry, or electron microscopy have been traditionally labeled PNETs, and those that are undifferentiated by these analyses have been diagnosed as Ewing's sarcoma."[3]
PNET of the CNS
PNET of the CNS generally refer to supratentorial PNETs.
- In the past medulloblastomas were considered PNETs; however, they are genetically, transcriptionally and clinically distinct. As such, "infratentorial" PNETs are now referred to as medulloblastoma[citation needed].
- Pineoblastomas are embryonal tumours originating in the pineal gland and are likely distinct from supratentorial PNETs.
Model
Using gene transfer of SV40 large T-antigen in neuronal precursor cells of rats, a brain tumor model was established. The PNETs were histologically indistinguishable from the human counterparts and have been used to identify new genes involved in human brain tumor carcinogenesis.[4] The model was used to confirm p53 as one of the genes involved in human medulloblastomas, but since only about 10% of the human tumors showed mutations in that gene, the model can be used to identify the other binding partners of SV40 Large T- antigen, other than p53.[5]
See also
References
- ↑ "primitive neuroectodermal tumor" at Dorland's Medical Dictionary
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ Kumar, Vinay; Fausto, Nelso; Abbas, Abul (2004) Robbins & Cotran Pathologic Basis of Disease (7th ed.). Saunders. Page 1301. ISBN 0-7216-0187-1.
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
