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CLINICAL PATHOLOGY UPDATE on SURAMADE I
Surabaya, 15th Juliy 2011




                            YETTI HERNANINGSIH, dr., SpPK
                              Clinical Pathology Department
                             Dr. Soetomo Hospital Surabaya
(Gorczyca W, Emmons FM, 2008)
                                2
Flow cytometric immunophenotyping is
          important for the
          Distinction between ALL and AML,
        identification of B-cell or T-cell lineage


      Assessing response to treatment, including
                 the detection of MRD


            Detection aberrant expression


                                                     3
SAMPLE STAINING
         1.SURFACE
           ANTIGEN

         2.INTRACELLULAR
           ANTIGEN (TdT,
           cCD3, cCD22,
           MPO)

         3.DNA CONTENT
                           4
5
6
(Gorczyca W, Emmons FM, 2008)
Immunophenotyping of AML
(Campana & Behm,2000)




                           7
(Courtesy Sayed DM)
                  8
9
Figure 6.22 Schematic illustration of antigen expression during normal T-cell and NK-cell
maturation. Note that, although the common lymphoid stem cell presumably arises in the bone
  marrow, most T-cell maturation occurs in the thymus. As with the B cells (Fig. 6.12), T-cell
            activation occurs after exposure to antigen.(Courtesy Dr. Dan Sabath.)
                                                                                               10
                          (Tkachuk DC, Hirschmann JV, 2007)
(Concise Manual of Hematology and Oncology, 2008)




                                                    11
(Concise Manual of Hematology and Oncology, 2008)




                                                    12
Biphenotypic Acute Leukemia




 If > 2 points is scored for both myeloid and one of the
  lymphoid lineages the case is classified as biphenotypic   13
Undifferentiated Acute Leukemias

 Rare subgroup of acute leukemias which cannot be
  further classified using the above mentioned criteria.
 Usually CD34+, HLA-DR+, CD38+, and CD7+.




                                                           14
ABERRANT




Immature B cell   Abberant : co express an antigen of
                  different lineage e.g. CD 65 (myeloid
                  antigen) expressed on an immature
                  B cell (CD19+, CD34+, cyCD22+,
                  cyCD79a+, TdT+)                     15
How to store and send sample for
         Immunophenotyping
              • Bone marrow (BM) aspirate or
Specimen        Whole blood (WB) with EDTA
              • No blood clot or hemolysis


Storage and   • At room temperature (never be
 Transport      transported on dry ice)


              • 24 hours, send to lab as soon as
 Stability      possible

                                                   16
How to store and send sample for
       Immunophenotyping

Hemogram   • Should be accompanied
             (if present)


Schedule   • Every working day


 Report
           • 1 working days
 issues
                                     17
Panel of antibodies recommended by European Group for the
Immunoloogical Characterization of aleukemia (EGIL) for
diagnosis and classificatin of acute leukemia (1995)




                                           (Courtesy Sayed DM)   18
Application of Immunophenotyping
      at Dr. Soetomo Hospital
 CD7 FITC/CD33 PE/CD45 PerCP


HLA-DR FITC/CD13 PE/CD45 PerCP


 CD19 FITC/CD10 PE/CD45 PerCP


  CD3 FITC/CD34 PE/CD45 PerCP


  CD5 FITC/CD20 PE/CD45 PerCP

                                   19
20
21
Positive expression :
  membran > 20%
  cytoplasmic >10%




                        22
Dr. SOETOMO HOSPITAL
      EXPERIENCES




                       23
Mrs.Sh, 44 y.o.




                  24
CD13, CD33, Anti-HLA-DR, CD34  POSITIVE
               Conclusion:
             Myeloid Lineage




                                           25
Mrs.Sm, 30 y.o.




                  26
CD13, Anti-HLA-DR, CD33, CD10  POSITIVE
           CML Conclusion:
 Myeloid Lineage Aberrant Expression CD10




                                            27
Mrs.Sl, 27 y.o.




                  28
CD33, CD13, Anti-HLA-DR, CD34, CD3, CD10, CD19 
                     POSITIVE
                    Conclusion:
Suspected Biphenotypic (Myeloid + B-Lymphoid) Acute
       Leukemia with Aberrant expression CD3




                                                      29
Mrs.M, 60 y.o.




                 30
AML-M5b
CD33, CD13, Anti-HLA-DR  POSITIVE
            Conclusion:
         Myeloid Lineage




                                     31
Mr.Ms, 24 y.o.




                 32
Anti-HLA-DR, CD10, CD19, CD34, CD3, CD20
                  POSITIVE
                  Conclusion:
B-Lymphoid Lineage with Aberrant Expression CD3

                                            CD13:
                                            13.9%




                                                    33
Mr.My, 51 y.o.




                 34
CD33, CD7, CD13, Anti-HLA-DR, CD34  POSITIVE
                  Conclusion:
 Myeloid Lineage with Aberrant Expression CD7




                                                35
WBC : 10.00 (90.8% Lymphocyte)
HGB : 7.2 23 y.o.
   Mr.Y,
PLT : 7




                                 36
Anti-HLA-DR, CD10, CD19, CD34, CD20
             POSITIVE
            Conclusion:
        B-Lymphoid Lineage




                                      37
Mr.I, 24 y.o.




                38
CD33, CD13, Anti-HLA-DR, CD10, CD19, CD34
                  POSITIVE
                 Conclusion:
Suspected Biphenotypic (Myeloid + B-Lymphoid)
               Acute Leukemia




                                                39
References
 Nguyen D, Diamond L.W, Braylan R.C. 2007. Flow
  Cytometry in Hematopathology. 2nd ed. Humara Press.
  New Jersey.
 Gorczyca W, Emmons F.N. 2008. Atlas of Differential
  Diagnostic in Neoplastic Hematopathology. 2nd ed.
  Genzyme Genetics. New York.
 Tkachuk D.C, Hirschmann J.V. 2007. Wintrobe Atlas of
  Clinical Hematology. 1st ed. Lippincott Williams & Wilkins.
 Berger DP, Engelhand m, Henβ H, Mertlesmann
  (eds.).2008. Concise Manual Hematology and Oncology.
  Springer. Heidelberg.
                                                                40
THANK
 YOU

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Ss9

  • 1. CLINICAL PATHOLOGY UPDATE on SURAMADE I Surabaya, 15th Juliy 2011 YETTI HERNANINGSIH, dr., SpPK Clinical Pathology Department Dr. Soetomo Hospital Surabaya
  • 2. (Gorczyca W, Emmons FM, 2008) 2
  • 3. Flow cytometric immunophenotyping is important for the Distinction between ALL and AML, identification of B-cell or T-cell lineage Assessing response to treatment, including the detection of MRD Detection aberrant expression 3
  • 4. SAMPLE STAINING 1.SURFACE ANTIGEN 2.INTRACELLULAR ANTIGEN (TdT, cCD3, cCD22, MPO) 3.DNA CONTENT 4
  • 5. 5
  • 9. 9
  • 10. Figure 6.22 Schematic illustration of antigen expression during normal T-cell and NK-cell maturation. Note that, although the common lymphoid stem cell presumably arises in the bone marrow, most T-cell maturation occurs in the thymus. As with the B cells (Fig. 6.12), T-cell activation occurs after exposure to antigen.(Courtesy Dr. Dan Sabath.) 10 (Tkachuk DC, Hirschmann JV, 2007)
  • 11. (Concise Manual of Hematology and Oncology, 2008) 11
  • 12. (Concise Manual of Hematology and Oncology, 2008) 12
  • 13. Biphenotypic Acute Leukemia  If > 2 points is scored for both myeloid and one of the lymphoid lineages the case is classified as biphenotypic 13
  • 14. Undifferentiated Acute Leukemias  Rare subgroup of acute leukemias which cannot be further classified using the above mentioned criteria.  Usually CD34+, HLA-DR+, CD38+, and CD7+. 14
  • 15. ABERRANT Immature B cell Abberant : co express an antigen of different lineage e.g. CD 65 (myeloid antigen) expressed on an immature B cell (CD19+, CD34+, cyCD22+, cyCD79a+, TdT+) 15
  • 16. How to store and send sample for Immunophenotyping • Bone marrow (BM) aspirate or Specimen Whole blood (WB) with EDTA • No blood clot or hemolysis Storage and • At room temperature (never be Transport transported on dry ice) • 24 hours, send to lab as soon as Stability possible 16
  • 17. How to store and send sample for Immunophenotyping Hemogram • Should be accompanied (if present) Schedule • Every working day Report • 1 working days issues 17
  • 18. Panel of antibodies recommended by European Group for the Immunoloogical Characterization of aleukemia (EGIL) for diagnosis and classificatin of acute leukemia (1995) (Courtesy Sayed DM) 18
  • 19. Application of Immunophenotyping at Dr. Soetomo Hospital CD7 FITC/CD33 PE/CD45 PerCP HLA-DR FITC/CD13 PE/CD45 PerCP CD19 FITC/CD10 PE/CD45 PerCP CD3 FITC/CD34 PE/CD45 PerCP CD5 FITC/CD20 PE/CD45 PerCP 19
  • 20. 20
  • 21. 21
  • 22. Positive expression : membran > 20% cytoplasmic >10% 22
  • 23. Dr. SOETOMO HOSPITAL EXPERIENCES 23
  • 25. CD13, CD33, Anti-HLA-DR, CD34  POSITIVE Conclusion: Myeloid Lineage 25
  • 27. CD13, Anti-HLA-DR, CD33, CD10  POSITIVE CML Conclusion: Myeloid Lineage Aberrant Expression CD10 27
  • 29. CD33, CD13, Anti-HLA-DR, CD34, CD3, CD10, CD19  POSITIVE Conclusion: Suspected Biphenotypic (Myeloid + B-Lymphoid) Acute Leukemia with Aberrant expression CD3 29
  • 31. AML-M5b CD33, CD13, Anti-HLA-DR  POSITIVE Conclusion: Myeloid Lineage 31
  • 33. Anti-HLA-DR, CD10, CD19, CD34, CD3, CD20  POSITIVE Conclusion: B-Lymphoid Lineage with Aberrant Expression CD3 CD13: 13.9% 33
  • 35. CD33, CD7, CD13, Anti-HLA-DR, CD34  POSITIVE Conclusion: Myeloid Lineage with Aberrant Expression CD7 35
  • 36. WBC : 10.00 (90.8% Lymphocyte) HGB : 7.2 23 y.o. Mr.Y, PLT : 7 36
  • 37. Anti-HLA-DR, CD10, CD19, CD34, CD20  POSITIVE Conclusion: B-Lymphoid Lineage 37
  • 39. CD33, CD13, Anti-HLA-DR, CD10, CD19, CD34  POSITIVE Conclusion: Suspected Biphenotypic (Myeloid + B-Lymphoid) Acute Leukemia 39
  • 40. References  Nguyen D, Diamond L.W, Braylan R.C. 2007. Flow Cytometry in Hematopathology. 2nd ed. Humara Press. New Jersey.  Gorczyca W, Emmons F.N. 2008. Atlas of Differential Diagnostic in Neoplastic Hematopathology. 2nd ed. Genzyme Genetics. New York.  Tkachuk D.C, Hirschmann J.V. 2007. Wintrobe Atlas of Clinical Hematology. 1st ed. Lippincott Williams & Wilkins.  Berger DP, Engelhand m, Henβ H, Mertlesmann (eds.).2008. Concise Manual Hematology and Oncology. Springer. Heidelberg. 40