HAEM5:Myelodysplastic neoplasm with biallelic TP53 inactivation: Difference between revisions

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{{DISPLAYTITLE:Myelodysplastic neoplasm with biallelic TP53 inactivation}}
{{DISPLAYTITLE:Myelodysplastic neoplasm with biallelic TP53 inactivation}}
[[HAEM5:Table_of_Contents|Haematolymphoid Tumours (5th ed.)]]
[[HAEM5:Table_of_Contents|Haematolymphoid Tumours (WHO Classification, 5th ed.)]]


==Primary Author(s)*==
==Primary Author(s)*==
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|'''Notes'''
|'''Notes'''
|-
|-
|EXAMPLE t(9;22)(q34;q11.2)
|<span class="blue-text">EXAMPLE:</span> t(9;22)(q34;q11.2)
|EXAMPLE 3'ABL1 / 5'BCR
|<span class="blue-text">EXAMPLE:</span> 3'ABL1 / 5'BCR
|EXAMPLE der(22)
|<span class="blue-text">EXAMPLE:</span> der(22)
|EXAMPLE 20% (COSMIC)
|<span class="blue-text">EXAMPLE:</span> 20% (COSMIC)


EXAMPLE 30% (add reference)
<span class="blue-text">EXAMPLE:</span> 30% (add reference)
|Yes
|Yes
|No
|No
|Yes
|Yes
|EXAMPLE
|<span class="blue-text">EXAMPLE:</span>


The t(9;22) is diagnostic of CML in the appropriate morphology and  clinical context (add reference). This fusion is responsive to targeted  therapy such as Imatinib (Gleevec) (add reference).
The t(9;22) is diagnostic of CML in the appropriate morphology and  clinical context (add reference). This fusion is responsive to targeted  therapy such as Imatinib (Gleevec) (add reference).