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**Infantile, p53 wildtype: Usu. desmoplastic/nodular, 10q loss. | **Infantile, p53 wildtype: Usu. desmoplastic/nodular, 10q loss. | ||
**SHH-p53 mutant: Usu. large cell/anaplastic, 17q loss. | **SHH-p53 mutant: Usu. large cell/anaplastic, 17q loss. | ||
*Group 3 (approx. 20%). | *Non WNT/Non SHH: | ||
**Classic and large cell/anaplastic, MYC amplification, isochromosome 17q. | **Group 3 (approx. 20%). | ||
*Group 4 (approx. 40%). | ***Classic and large cell/anaplastic, MYC amplification, isochromosome 17q. | ||
**Classic phenotype, MYCN amplification, isodicentric 17q. | **Group 4 (approx. 40%). | ||
***Classic phenotype, MYCN amplification, isodicentric 17q. | |||
Note: Within Group 3+4 two or more of chromosome 7 gain, chromosome 8 loss, and chromosome 11 loss separates standard risk medulloblastoma samples into favorable and classifies the remaining i17q diploid cases as high-risk. | |||
==Prognosis== | ==Prognosis== |