Table of frequent aberrant markers in AML: Difference between revisions
From haematologyetc.co.uk
No edit summary |
No edit summary |
||
Line 8: | Line 8: | ||
---- | ---- | ||
The key point is that AML will frequently express immunological markers not typically associated with myeloid lineage. Broadly, the abberant expression may include: | |||
Markers of primitive phenotype that are more frequently associated with lymphoid disorders, most | Markers of primitive phenotype that are more frequently associated with lymphoid disorders, This is aknowledged in diagnostic criteria and providing diagnostic criteria are applied they do not require a changed diagnosis. | ||
The most frequent "abberencies" observed in AML are:</br> | |||
</br>(1) The expression of CD7 by nearly half of cases | |||
</br>(2) The expression of CD19, often associated with particular AML subtypes | |||
----- | |||
CD19 BCRABL TdT 7% | |||
Markers associated with lymphoid maturation that may also be expressed by the lineage maturation, particularly monocytic lineage | Markers associated with lymphoid maturation that may also be expressed by the lineage maturation, particularly monocytic lineage |
Revision as of 17:21, 12 January 2024
The key point is that AML will frequently express immunological markers not typically associated with myeloid lineage. Broadly, the abberant expression may include:
Markers of primitive phenotype that are more frequently associated with lymphoid disorders, This is aknowledged in diagnostic criteria and providing diagnostic criteria are applied they do not require a changed diagnosis.
The most frequent "abberencies" observed in AML are:
(1) The expression of CD7 by nearly half of cases
(2) The expression of CD19, often associated with particular AML subtypes
CD19 BCRABL TdT 7%
Markers associated with lymphoid maturation that may also be expressed by the lineage maturation, particularly monocytic lineage CD2 CD4, 36 38 MONOCYTIC 5%
BASOPHILIC 123, 203, 11B 22
Frequent abberant markers in AML that are often associated with genetic/cytogenetic subtype: CD19 30% CBF RUNX1, BCRABL CD56 CBF RUNX1 NPM1 OFTEN LACK CD34