AML (Acute Myelogenous Leukemia without maturation) (M1)From $1Table of contents
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EpidemiologyAML-M1 comprises approximately 10% of AMLs. It may occur at any age but the majority of patients are adults. The median age is 46 years of age. MorphologyIn some cases the immature cells have abundant, frequently basophilic cytoplasm, with variable numbers of often indistinct, sometimes coalescent granules. If such immature cells are < 10% the diagnosis is M1, but if > 10% the diagnosis becomes M2.
ImmunophenotypingUsing a CD45 vs SSC gating dot plot, blasts can be identified (green population below). Myeloblasts M1 have moderate CD45 expression and low to moderate SSC. Note these blasts have a slightly higher SSC than the lymphocytes (red population below).
Below are selected example histograms from a case of AML M1.
The M1 blasts express at least two of the following myeloid antigens: CD13, CD33, CD117, MPO and/or HLA-DR. CD34 is often positive. There is generally no expression of the monocytoid markers CD11b or CD14. Lymphoid antigens CD3, CD20, CD79a are absent. CD7 may be expressed. Other relevant testsCytochemistry: Relatively few blasts (5-10%) are MPO (myeloperoxidase) positive. A minimum of 3% MPO positive blasts are required for diagnosis. NSE and PAS are generally negative. Genetics: Chromosome Abnormalities: t(9;22) Philadelphia chromosome, 8+, -5, and -7. Flow DiagnosisAML-M1 and AML-M2 are initially stratified by morphology (see above). M1 blasts must express at least two of the following myeloid antigens: CD13, CD33, CD117, MPO and/or HLA-DR. MPO must be expressed on > 3% on blasts.
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Page last modified 06:44, 21 Jun 2008 by Teri
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