Difference between revisions of "Chromosomal translocations"
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| t(11;22) | | t(11;22) | ||
| FLI1-EWS | | FLI1-EWS | ||
| <ref name=Ref_PBoD8_1249>{{Ref PBoD8|1249}}</ref> | | <ref name=Ref_PBoD8_1249>{{Ref PBoD8|1249}}</ref><ref name=OMIM133450>{{OMIM|133450}}</ref> | ||
|- | |- | ||
| Myxoid liposarcoma, round-cell type liposarcoma | | Myxoid liposarcoma, round-cell type liposarcoma | ||
| t(12;16) | | t(12;16) | ||
| CHOP-TLS | | CHOP-TLS | ||
| <ref name=Ref_PBoD8_1249>{{Ref PBoD8|1249}}</ref><ref>{{cite journal |author=Antonescu CR, Tschernyavsky SJ, Decuseara R, ''et al.'' |title=Prognostic impact of P53 status, TLS-CHOP fusion transcript structure, and histological grade in myxoid liposarcoma: a molecular and clinicopathologic study of 82 cases |journal=Clin. Cancer Res. |volume=7 |issue=12 |pages=3977–87 |year=2001 |month=December |pmid=11751490 |doi= |url=}}</ref> | | <ref name=Ref_PBoD8_1249>{{Ref PBoD8|1249}}</ref><ref>{{cite journal |author=Antonescu CR, Tschernyavsky SJ, Decuseara R, ''et al.'' |title=Prognostic impact of P53 status, TLS-CHOP fusion transcript structure, and histological grade in myxoid liposarcoma: a molecular and clinicopathologic study of 82 cases |journal=Clin. Cancer Res. |volume=7 |issue=12 |pages=3977–87 |year=2001 |month=December |pmid=11751490 |doi= |url=}}</ref><ref name=OMIM613488>{{OMIM|613488}}</ref> | ||
|- | |- | ||
| [[Synovial sarcoma]] | | [[Synovial sarcoma]] | ||
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| ETV6-NTRK3 | | ETV6-NTRK3 | ||
| <ref name=Ref_PBoD8_1249>{{Ref PBoD8|1249}}</ref> | | <ref name=Ref_PBoD8_1249>{{Ref PBoD8|1249}}</ref> | ||
|} | |||
===EWS associated=== | |||
{| class="wikitable sortable" style="margin-left:auto;margin-right:auto" | |||
| '''Tumour''' | |||
| '''Translocation(s)''' | |||
| '''Genes''' | |||
| '''Reference(s)''' | |||
|- | |||
| [[Ewing sarcoma]]/PNET | |||
| t(11;22) | |||
| FLI1-EWS | |||
| <ref name=Ref_PBoD8_1249>{{Ref PBoD8|1249}}</ref><ref name=OMIM133450>{{OMIM|133450}}</ref> | |||
|- | |||
| Extraskeletal myxoid [[chondrosarcoma]] | |||
| t(9;22) | |||
| CHN-EWS | |||
| <ref name=Ref_PBoD8_1249>{{Ref PBoD8|1249}}</ref> | |||
|- | |||
| [[Desmoplastic small round cell tumour]] | |||
| t(11;22) | |||
| EWS-WT1 | |||
| <ref name=Ref_PBoD8_1249>{{Ref PBoD8|1249}}</ref> | |||
|- | |||
| [[Clear cell sarcoma]] | |||
| t(12;22) | |||
| EWS-ATF1 | |||
| <ref name=Ref_PBoD8_1249>{{Ref PBoD8|1249}}</ref> | |||
|- | |||
|} | |} | ||
Revision as of 06:05, 30 April 2011
Chromosomal translocations, also translocations, may be characteristic of a tumour or simply narrow down the diagnosis to a set of tumours.
Key point
The key point is:
- One should be aware of the existence of specific (i.e. diagnostic/near diagnostic) translocations and translocations which significantly narrow down the diagnosis -- which are available to (clinical) pathologists.
Unfortunate reality of residency
Translocations are often a subject of pimping and show-up on examinations.
List of translocations
Soft tissue table
Tumour | Translocation(s) | Genes | Reference(s) |
Ewing sarcoma/PNET | t(11;22) | FLI1-EWS | [1][2] |
Myxoid liposarcoma, round-cell type liposarcoma | t(12;16) | CHOP-TLS | [1][3][4] |
Synovial sarcoma | t(X;18) | SYT-SSX | [1] |
Alveolar rhabdomyosarcoma | t(1;13) t(2,13) |
PAX7-FKHR PAX3-FKHR |
[1] |
Extraskeletal myxoid chondrosarcoma | t(9;22) | CHN-EWS | [1] |
Desmoplastic small round cell tumour | t(11;22) | EWS-WT1 | [1] |
Clear cell sarcoma | t(12;22) | EWS-ATF1 | [1] |
Dermatofibrosarcoma protuberans | t(17;22) | COLA1-PDGFB | [1] |
Alveolar soft part sarcoma | t(X;17) | TFE3-ASPL | [1] |
Congenital fibrosarcoma | t(12;15) | ETV6-NTRK3 | [1] |
EWS associated
Tumour | Translocation(s) | Genes | Reference(s) |
Ewing sarcoma/PNET | t(11;22) | FLI1-EWS | [1][2] |
Extraskeletal myxoid chondrosarcoma | t(9;22) | CHN-EWS | [1] |
Desmoplastic small round cell tumour | t(11;22) | EWS-WT1 | [1] |
Clear cell sarcoma | t(12;22) | EWS-ATF1 | [1] |
Paediatric table
Translocation | Genes | Tumour(s) | Reference |
t(12;16) | FUS/ATF1 | angiomatoid fibrous histiocytoma | [5] |
t(12;22) | EWS/ATF1 | angiomatoid fibrous histiocytoma | [5] |
t(12;16) | EWS/CHOP | myxoid liposarcoma | [5] |
t(16;22) | EWS/ATF1 | myxoid liposarcoma | [5] |
t(12;22) | EWS/ATF1 | clear cell sarcoma | [5] |
t(21;22) | EWS/ATF1 | Ewing sarcoma | [5] |
t(12;21) | FUS/ERG | Ewing sarcoma | [5] |
t(12;21) | FUS/ERG | acute myeloid leukemia | [5] |
See also
References
- ↑ 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 1.13 Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson; Aster, Jon (2009). Robbins and Cotran pathologic basis of disease (8th ed.). Elsevier Saunders. pp. 1249. ISBN 978-1416031215.
- ↑ 2.0 2.1 Online 'Mendelian Inheritance in Man' (OMIM) 133450
- ↑ Antonescu CR, Tschernyavsky SJ, Decuseara R, et al. (December 2001). "Prognostic impact of P53 status, TLS-CHOP fusion transcript structure, and histological grade in myxoid liposarcoma: a molecular and clinicopathologic study of 82 cases". Clin. Cancer Res. 7 (12): 3977–87. PMID 11751490.
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) 613488
- ↑ 5.0 5.1 5.2 5.3 5.4 5.5 5.6 5.7 PST. 14 February 2011.