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The second edition of this volume reflects the recent advances in the FCM analysis of hematopoietic disorders. The chapters have been revised to incorporate new text and figures. The volume is aimed at hematopathologists, hematologists, pathologists, and laboratory technicians.

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Produktbeschreibung
The second edition of this volume reflects the recent advances in the FCM analysis of hematopoietic disorders. The chapters have been revised to incorporate new text and figures. The volume is aimed at hematopathologists, hematologists, pathologists, and laboratory technicians.

Dieser Download kann aus rechtlichen Gründen nur mit Rechnungsadresse in A, B, BG, CY, CZ, D, DK, EW, E, FIN, F, GR, HR, H, IRL, I, LT, L, LR, M, NL, PL, P, R, S, SLO, SK ausgeliefert werden.

  • Produktdetails
  • Verlag: Springer-Verlag GmbH
  • Erscheinungstermin: 4. März 2008
  • Englisch
  • ISBN-13: 9781597451628
  • Artikelnr.: 37341224
Autorenporträt
Raul C. Braylan, University of Florida College of Medicine, Gainesville, FL, USA
Inhaltsangabe
Table of Contents

Preface to second edition
Preface to first edition
Acknowledgements
List of Abbreviations
List of Case Studies
Color Plates

Chapter 1 Approach to Flow Cytometry - General Considerations

1.1 Reasons for the necessity of proper data analysis
1.1.1 The pitfalls of the FCM data format of 'percent positive' per
antibody tested
1.2 General aspects of FCM data analysis and interpretation
1.3 Other applications of FCM in hematopathology
1.4 Maturation and differentiation of hematopoietic elements, an
overview based on the immunologic markers currently in use in the FCM
laboratory

Chapter 2 FCM immunophenotyping and DNA analysis - Practical aspects
that can affect data analysis and interpretation

2.1 Sample selection
2.1.1 Liquid specimens
2.1.2 Solid tissue specimens
2.2 Preparing nucleated cell suspensions
2.3 Cell yield and viability
2.4 Sample staining.
2.4.1 Surface antigens
2.4.2 Intracellular antigens
2.4.3 DNA content
2.5 Data acquisition
2.5.1 Calibration
2.5.2 Color compensation
2.5.3 List mode data collection
2.5.4 Exclusion of nonviable cells
2.6 Antibody panel design
2.6.1 Antibody selection
2.6.1.1 Anti-light chain antibodies
2.6.2 Fluorochrome conjugation
2.7 Comprehensive antibody panels
2.7.1 Disease-oriented antibody panels
2.7.2 Antibody panels oriented by specimen type
2.8 Tailored panels and add-on testing
2.8.1 Minimal residual disease
2.9 FCM immunophenotyping data representation
2.9.1 Analysis panels
2.9.2 Color display
2.10 Approach to DNA data analysis
2.10.1 DNA ploidy
2.10.2 S-phase

Chapter 3 FCM data analysis on nearly homogeneous samples

3.1 FCM parameters
3.1.1 Forward scatter
3.1.2 Side scatter
3.1.3 Fluorescence
3.1.3.1 Heterogeneous fluorescence intensity (bimodal, variable)
3.2 Fluorescence dynamic range
3.3 Strategy to the visual review of FCM immunophenotyping data
3.4 Common SSC/CD45 patterns
3.4.1 Assessment of the blast population
3.4.2 Immature neoplastic cells with downregulated CD45
3.4.3 SSC/CD45 in mature lymphoid disorders
3.5 Other dot plot patterns useful in acute leukemia diagnosis
3.5.1 Useful antigenic features in AML
3.5.1.1 Myeloid phenotypic abnormalities and MRD detection
3.5.2 Precursor B-ALL vs bone marrow B-cell progenitors
3.5.3 Useful antigenic features in precursor T-lymphoma/leukemia
3.6 Evaluation of mature lymphoid malignancies
3.6.1 Assessment of surface light chain expression
3.6.2 Assessment of pan B-cell antigens
3.6.3 Useful antigenic features in mature B-cell malignancies
3.6.3.1 CD10 expression: Follicular center cell lymphomas
3.6.3.2 Pattern of CD20 and CD11c coexpression
3.6.3.3 CD5 expression
3.6.3.4 Aberrant B-cell profile
3.6.4 Identification of abnormal mature T-cells
3.6.5 Useful antigenic features in mature T-cell malignancies
3.7 Assessing the biological behavior of mature lymphoid neoplasms
3.8 Dot plot patterns in histiocytic proliferations and
nonhematopoietic malignancies

Chapter 4 FCM data analysis on heterogeneous specimens

4.1 Identifying normal FCM samples
4.1.1 Benign/reactive solid lymphoid tissue (e.g., lymph nodes,
tonsils)
4.1.1.1 Pattern of CD10/CD20 coexpression. Distinction between FRFH
and FCC lymphoma
4.1.2 Normal peripheral blood and normal bone marrow
4.1.2.1 Blast region
4.1.2.2 Bone marrow B-cell precursors
4.1.2.3 Lymphocytes
4.1.2.4 Monocytes
4.1.2.5 Plasma cells
4.1.2.6 Erythroid precursors
4.1.2.7 Maturing myeloid cells
4.2 Abnormal heterogeneous samples with a detectable immature
neoplastic population
4.2.1 Blasts of lymphoid lineage
4.2.2 Blasts of myeloid lineage
4.2.2.1 AML
4.2.2.2 High-grade MDS and MPD with increased blasts
4.3 Minimal residual disease
4.4 Abnormal heterogeneou
Rezensionen
"The first edition of this book was wonderful, and this updated edition continues the tradition of excellence. You need this book for ready access if you do hematopathology." -Doody's Book Review, Weighted Numerical Score:96 - 4 Stars

From the reviews of the second edition:

"The book is nicely illustrated and contains numerous colour figures illustrating the broad variety of flow cytometry applications in various haematological conditions. ... The book is very well suited for clinical pathologists, assistants in training in the field of laboratory medicine and clinical pathology, medical technicians and researchers working in clinical haematology laboratories, as well as clinical haematologists who want to get familiar with the recent evolutions in ... diagnostic laboratory medicine." (Joris Delanghe, Acta Clinica Belgica, Vol. 63 (2), 2008)