Glad you have received some positive news Jeanie.  Are you waiting for
more results, or do these results allow you to relax a bit?  God
bless, Kathy

On Feb 4, 3:30 pm, [EMAIL PROTECTED] wrote:
> Thanks,
> I thought it sounded good but my platelets are still a little high; 509 on  
> this test; WBC 7.9.
> I can't understand why on some test there are no abnormal cells and on  other
> test there are.
> It's confusing.
> Thanks again,
> Jeanie<3
> In a message dated 2/4/2008 11:00:20 A.M. Pacific Standard Time,  
>
> [EMAIL PROTECTED] writes:
>
> No  abnormal cells is good.
>
> Polyclonal is good.  It means a diverse  population of lymphocytes
> instead of an expansion of a single clone  (leukemia).  Most
> Lymphocytic leukemias are B-cell in  origin
>
> Granulocytic cells are your Neutrophils, Eosinophils, and  Basophils.
> No problems there.  Immature granulocytic (aka myeloid)  cells which
> can be indicative of other leukemias can be detected by  flow
> cytometry.
>
> In cytometry, your cells are divided among a bunch  of tubes and test
> reagents are added that have fluroescent dyes  attached.  Each tube is
> labeled with the names of the tests and about  6 can be added to each
> tube.  Then the cells are sucked up into the  cytometer and passed thru
> a laser beam.  Cells are measured by the way  they bend the laser light
> and also what type of flurescence light they  emit.
>
> Gating is just the way the results are sorted out on the  computer.
> Each cell that is analyzed on the cytometer (it can read about  10,000
> a second) are stored in a computer file and its one file per  test
> tube.  The technician then goes back in the computer and puts  gates
> (boxes) around the cell populations and asks the computer to show  the
> results just for the cells in the gate.  On a cytometer, the  cell
> populations form kind of an arc on the screen with the lymphocytes  in
> the lower left, the monocytes mid right, and the granulocytes in  the
> upper middle to upper right.  The idea with gating is just to look  at
> what is of interest depending on the test reagents that were put  into
> that tube.  If the tube had no lympocyte-specific reagents in it,  then
> there is no need to even count the lymphocytes in the  analysis.
>
> A common test for clonal B-cell expansion is to test CD5 and  CD19
> (CD20) in the same tube. CD5 is usually only on T-cells.  CD19 is  on
> all B-cells and CD20 is only on mature B-cells.  Every person  with
> Chronic Lymphocytic Leukemia will have leukemia cells that  exhibit
> both CD5 and CD19 (or CD20) on the same cell.  That is not  normal.  If
> each reagent was done separately, one might be able to  infer that
> something was wrong since the % of B-cells in the blood was way  too
> high but this simple combination confirms the diagnosis  immediately.
> Cytometry can be quite useful as a screening tool of the  blood.
>
> This report looks great.
>
> On Feb 4, 1:01 pm, [EMAIL PROTECTED] wrote:
>
>
>
>
>
>
>
> > Hi all,
> > Here is the results of the  FLOW CYTOMETRY REPORT done on my Peripheral  
> blood.
> >  IMMUNOPHENOTYPE REPORT
> > SPECIMEN : Peripheral blood
>
> >  INTERPRETATION
> > There is no immunophenotypic evidence of an abnormal  population of  cells.
> > IMMUNOPHENOTYPE (of relevant population);  Polyclonal B-lymphocytes, normal
> > T-lymphocytes and granulocytic  cells are identified.
> > ANALYTICAL GATING:
> > Gating was performed  on the granulocytic, blast, monocytic and
> lymephocytic  
> >  region
> > MORPHOLOGY:
> > Review of the peripheral blood smear  demonstrates no evidence of  
> circulating
> > abnormal cells
> >  CLINICAL DATA:
> > The patient is a 69 year old female with history of  thrombocytosis and  
> > leukocytosis
> > Can someone explain  this to me.
> > Thanks,
> > Jeanie<3
>
> **************Biggest Grammy Award surprises of all time on AOL Music.    
> (http://music.aol.com/grammys/pictures/never-won-a-grammy?NCID=aolcmp0...
> 48)- Hide quoted text -
>
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