Recurrent Genomic Alterations in Pediatric and Adult Central Nervous System Tumors Detected by Chromosomal Microarray: Difference between revisions
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Created page with "==Recurrent Genomic Alterations in AML Detected by Chromosomal Microarray (Literature Review)== Table 1 - A comprehensive list of CNAs and CN-LOH detectable by CMA testing wi..." |
Adding CNS Tumor information |
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==Recurrent Genomic Alterations in | ==Recurrent Genomic Alterations in Pediatric and Adult CNS Detected by Chromosomal Microarray (Literature Review)== | ||
Table 1 - | Table 1 - Pediatric Central Nervous System Tumors. Table derived from Ligon et al., 2018 [ ] with permission from Cancer Genetics. | ||
{| class="wikitable" | {| class="wikitable" | ||
|- | |- | ||
! | ! TUMOR | ||
! | ! SUBTYPES | ||
! | ! BROAD ABERRATIONS (>10Mb) | ||
! | ! FOCAL ABERRATIONS (>10Mb) | ||
! | ! CLINICAL FEATURES | ||
! REFERENCES | |||
|- | |||
! GLIOMAS | |||
|- | |||
| Low grade glioma, WHO grade I | |||
| Pilocytic astrocytoma/pilomyxoid astrocytoma | |||
| Some tumors show polysomy 7; other polysomies more common in adult PA | |||
| '''Fusions:''' KIAA1549-BRAF fusion (via 3'BRAF duplication), other BRAF partners reported; NTRK fusions (rare); FGFR1 fusions (rare); '''Mutations:''' BRAF V600E (particularly extra-cerebellar tumors); FGFR1 (midline PA); NF1 (esp. germline), other MAPK pathway mutations '''Loss:''' NF1 in optic pathway PA | |||
| Classic PA are cerebellar (most commonly associated with BRAF duplication); PA in patients with germline NF1 alterations often develop as optic gliomas;Surgical resection can be curative; PMA generally more aggressive than PA; BRAF fusions and BRAF mutations generally are mutually exclusive | |||
| PMID:19016743; PMCID:2761618; PMID:18716556 PMID:25461780 PMID:25664944; PMID:26378811 PMCID:3429698; PMID:23817572; PMID:23583981 PMID:18974108; PMID:23278243; PMID:21274720 | |||
|- | |- | ||
| AML including NK-AML | | AML including NK-AML | ||
| CN-LOH | | CN-LOH | ||