Autor: Mike Leach, Mark Drummond, Allyson Doig, Pam McKay, Bob Jackson, Barbara J. Bain
Wydawca: Wiley
Dostępność: 3-6 tygodni
Cena: 549,15 zł
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ISBN13: |
9781118747032 |
ISBN10: |
1118747038 |
Autor: |
Mike Leach, Mark Drummond, Allyson Doig, Pam McKay, Bob Jackson, Barbara J. Bain |
Oprawa: |
Hardback |
Rok Wydania: |
2015-07-10 |
Ilość stron: |
414 |
Wymiary: |
246x189 |
Tematy: |
MJ |
The analysis of blood, bone marrow and tissue fluid specimens requires a multi–faceted approach with the integration of scientific data from a number of disciplines. No single discipline can operate in isolation or errors will occur. Flow cytometry is in a privileged position in that it can provide rapid analysis of specimens and it is often the first definitive investigation to produce results and help formulate a working diagnosis.
This companion text to Practical Flow Cytometry in Haematology Diagnosiscontains 100 worked examples drawn from real clinical cases presenting to the authors institution. Cases are illustrated with peripheral blood and bone marrow cytology, tissue pathology and cytogenetic and molecular data, which are integrated to generate, where appropriate, a diagnosis based on the WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. The spectrum of clinical cases includes adult and paediatric patients, and both neoplastic and reactive disorders. The cases appear in no particular order to challenge the reader to make their own diagnosis.
The reader will review May Grünwald Giemsa (MGG)–stained films of peripheral blood and bone marrow aspirates presented alongside flow cytometric data and haematoxylin and eosin (H&E)–stained bone marrow and other tissue biopsy sections. Immunohistochemistry is used to further clarify the tissue lineage and cell differentiation. Cytogenetic studies using metaphase preparations are used to identify translocations and chromosome gains and losses whilst interphase fluorescence in situ hybridisation (FISH) studies and polymerase chain reaction (PCR) are used to identify gene fusions, gene rearrangements and deletions. Each case concludes with a discussion of the features that are important to making a diagnosis. The cases are also listed according to disease classification in the appendix so that the text can also be used as a reference.
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