View source for Atypical patterns of primitive marker expression in acute myeloid leukaemia

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| colspan="1"''|[[The flow cytometric diagnosis of AML|Return to previous page]]''
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Atypical marker patterns associated with specific AML subtypes

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|colspan="1" style = "font-size:90%; color:black; background:#ddeee1"|While blast cells typically cause low side scatter of light and have an expression of CD45 that is lower than normal lymphocytes or monocytes, atypical pattterns may cause difficulty. These are often associated with particular AML subtypes. 
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|colspan="1" style = "font-size:90%;"|'''AML with monocytic differentiation'''</br>In AML with monocytic maturation those primitive cells with more mature monocytic features may show higher side scatter (consistent with their size and cytological features) and some or all of the blast cells may also have high expression of CD45 (comparable with normal or CMML monocytes). In such cases the neoplastic cells may lie in the typical monocyte area, and so are difficult to distinguish from reactive monocytes, or from typical or transforming CMML. It is important to compare with clinical and morphological features to ensure appropriate classification ([[Recognition of blast cells with monocytic differentiation|click for further detail]]).
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|colspan="1" style = "font-size:90%;|'''Acute promyelocytic leukaemia'''</br>Cells of APL can vary in size and granularity an will often express a range of side scatter features may resemble those of maturing granulocytic cells, similarly CD45 expression may be similar to maturing granulocytic cells. The distribution of cells will be abnormal however and may variably include cells with wide range light scatter features that differ from those of typical blast cells. It is important to distinguish APL blasts from reactive myeloid cells or (in some cases) from cells of MDS. Morphological examination is essential, but consider also the pattern of additional markers ([[Recognition of APL differentiation|click for further detail]]).
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|colspan="1" style = "font-size:90%;"|'''Other patterns'''</br> While most frequently blast cells with myeloid differentiation form a relatively homogenous group with moderately weak CD45 expression, in some cases very weak expression may be seen, or CD45 may have a broad width of expression. These patterns may more closely resemble the appearances of ALL or even of non-haematopoietic tumours. Stronger CD45 expression may also occasionally be seen.
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<div id="AML_MonoPic">'''Recognition of blast cells with monocytic differentiation'''</div>

[[Image:AMLM5A.jpg|130px|caption]] '''A''' monoblastic AML
[[Image:AMLM5B.jpg|130px|caption]] '''B''' monocytic AML 

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*'''Panel A''': Where cells have a monoblastic differentiation (generally large blast cells with primitive chromatin and nucleoli that lack ''monocytic shape'' often with basophilic cytoplasm) the monoblasts tend to express markers of primitive phenotype, while typical antigens of monocytic differentiation may be variable or weakly expressed.
*'''Panel B''': Where cells undergo more appreciable monocytic differentiation (note the more condensed chromatin, lack of nucleolus, and ''monocytic shape'' of there nucleus) these cells tend to have stronger CD45 expression and often express typical monocyte antigens, primitive markers may be variably expressed or absent. 
*Mixed patterns of monoblastic monocytic and myeloid differentiation within the same case are also frequently found. 

:''Correlation of immunophenotype with morphology and clinical features may be necessary to accurately identify such cells as blasts.''
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<div id="AML_AplPic">'''Recognition of acute promyelocytic leukaemia'''</div>

[[Image:AML M1.png|130px]]  

<span style="font-size:90%">Typical APL has cells that are hypergranular (A) or may be the microgranular variant (B) generally the cells will have a range of granulation or nuclear appearance. While CD45 expression tends to be weak, in almost all cases the variable morphological features cause a wide range of side-scatter with the abnormal cells often forming a "cloud" extending toward the neutrophil area. This can make the cells (particular hypergranular forms) difficult to distinguish from reactive myeloid populations (or occasionally from MDS). Absent HLA-DR on APL cells can help distinguish from reactive cells (expressing HLA-DR), but correlation with morphology and clinical features and other confirmatory tests are essential to the recognition of APL.''</span>

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