Kaushansky: Williams Hematology 8th Edition with CD






The rate of growth in our understanding of diseases of blood cells and coagulation proteins provides a challenge for the editors of a comprehensive textbook of hematology. The sequencing of individual genomes and the acquisition of knowledge in proteomics, metabolomics, and all the other burgeoning "-omics" fields as applied to hematologic disorders have accelerated the understanding of the pathogenesis of the diseases of our interest. The rate at which basic knowledge in molecular and cell biology and molecular immunology has been translated into improved diagnostic and therapeutic methods is equally impressive. Specific molecular targets for therapy in a myriad of hematological disorders have become reality, and it is not hyperbole to state that hematology has become the poster child for the rational design of therapeutics throughout all of medicine. 

This edition of Williams Hematology includes many changes, for the better. Each chapter has been extensively revised or rewritten to provide the most current information available. Two new chapters have been added, Chapter 10 entitled Epigenetics and Genomics, to reflect the growing importance of this basic science in hematology, and Chapter 28 entitled Principles of Multipotential Cell Therapy for Tissue Replacement. In addition, several chapters have been divided, most notably the single chapter on non-Hodgkin lymphoma has been split into its constituent diseases, and the chapters on erythrocytosis and thrombocytosis have been divided into the myeloproliferative and reactive forms, to reflect our growing understanding of the pathophysiology of these disorders and more targeted approaches to their therapy. Recognizing that at the heart of hematology is blood and marrow cell morphology, the authors have incorporated most of the collection of 274 images that appeared in a separate section of color plates in the 7th edition (as well as additional images) into the relevant topics in each chapter, allowing far easier access to highly informative illustrations and cellular morphology.

Apropos the age of information, the new edition of Williams Hematology is also available online, as part of the popular www.accessmedicine.com website. With direct links to a comprehensive drug therapy database and to other important medical texts, including Harrison's Principles of Internal Medicine and Goodman and Gilman's The Pharmacological Basis of Therapeutics, Williams Hematology Online is part of a powerful resource covering all disciplines within medical education and practice. The online edition of Williams Hematology also includes PubMed links to journal articles cited in the references in our new edition.

For the first time, a CD accompanies the Williams Hematology book. The CD features a large selection of morphologies, illustrations, and drawings, from this new edition of Williams Hematology; these can be easily transported into PowerPoint™ format for use in lectures and presentations. 

Finally, the Williams Manual of Hematology will once again be revised. The convenient Manual features the most clinically salient content from the parent text, and is perfect for use in time-restricted clinical situations. The Manual will be available for iPhone™ and other mobile formats. 

The readers of the 8th edition of Williams Hematology will note the passing of a legend in hematology, Dr. Ernest Beutler. Ernie was a founding editor and the lead editor of Hematology for the 5th and 6th editions, continued to contribute as an editor for the 7th edition, and passed away in October 2008, while the 8th edition's revised and new chapters were being compiled. Ernie's thumbprint continues to permeate the 8th edition, including F1 and F2 generations of the Beutler pedigree, and it is to Ernie that dedicate this edition.

New to this Edition:
  • Full-color presentation conveniently integrates images of blood and tissue findings where they are cited in the text.
  • Two additional chapters, “Genomics and Epigenetics,” and “Regenerative Medicine: Principles of Multipotential Cell Therapy for Tissue Replacement,” offer insights into the application of genomic and monoclonal therapies to hematology and emphasize their role in improving diagnostic and therapeutic methods.
  • Expanded coverage of non-Hodgkin lymphoma includes separate chapters on its constituent diseases, providing an in-depth assessment of the diagnosis and management of these disorders.
  • A comprehensive discussion of erythrocytosis and thrombocytosis reviews reactive and malignant forms of myeloproliferation, encompassing new genetic advances in these disorders along with more targeted therapeutic approaches.
  • Companion CD includes a large selection of morphologies, illustrations, and drawings from the book, in a presentation-ready PowerPoint format. 

Contents
Part I. Clinical Evaluation of the Patient
  • Chapter 1 Initial Approach to the Patient: History and Physical Examination
  • Chapter 2 Examination of Blood Cells
  • Chapter 3 Examination of the Marrow
Part II. The Organization of the Lymphohematopoietic Tissues
  • Chapter 4 Structure of the Marrow and the Hematopoietic Microenvironment
  • Chapter 5 The Organization and Structure of Lymphoid Tissues
Part III. Epochal Hematology
  • Chapter 6 Hematology of the Fetus and Newborn
  • Chapter 7 Hematology during Pregnancy
  • Chapter 8 Hematology in Older Persons
Part IV. Molecular and Cellular Hematology
  • Chapter 9 Genetic Principles and Molecular Biology
  • Chapter 10 Genomics and Epigenetics
  • Chapter 11 Cytogenetics and Molecular Abnormalities
  • Chapter 12 Apoptosis
  • Chapter 13 Cell-Cycle Regulation and Hematologic Disorders
  • Chapter 14 Signal Transduction Pathways
  • Chapter 15 The Cluster of Differentiation Antigens
  • Chapter 16 Hematopoietic Stem Cells, Progenitors, and Cytokines
  • Chapter 17 The Inflammatory Response
  • Chapter 18 Innate Immunity
  • Chapter 19 Dendritic Cells and the Control of Innate and Adaptive Immunity
Part V. Therapeutic Principles
  • Chapter 20 Pharmacology and Toxicity of Antineoplastic Drugs
  • Chapter 21 Principles of Hematopoietic Cell Transplantation
  • Chapter 22 Treatment of Infections in the Immunocompromised Host
  • Chapter 23 Principles of Antithrombotic Therapy
  • Chapter 24 Principles of Immune Cell Therapy
  • Chapter 25 Principles of Vaccine Therapy
  • Chapter 26 Principles of Therapeutic Apheresis: Indications, Efficacy, and Complications
  • Chapter 27 Principles of Gene Transfer for Therapy
  • Chapter 28 Regenerative Medicine: Principles of Multipotential Cell Therapy for Tissue Replacement
Part VI. The Erythrocyte
  • Chapter 29 Morphology of the Erythron
  • Chapter 30 Composition of the Erythrocyte
  • Chapter 31 Production of Erythrocytes
  • Chapter 32 Destruction of Erythrocytes
  • Chapter 33 Clinical Manifestations and Classification of Erythrocyte Disorders
  • Chapter 34 Aplastic Anemia: Acquired and Inherited
  • Chapter 35 Pure Red Cell Aplasia
  • Chapter 36 Anemia of Chronic Renal Disease
  • Chapter 37 Anemia of Chronic Disease
  • Chapter 38 Anemia of Endocrine Disorders
  • Chapter 39 The Congenital Dyserythropoietic Anemias
  • Chapter 40 Paroxysmal Nocturnal Hemoglobinuria
  • Chapter 41 Folate, Cobalamin, and Megaloblastic Anemias
  • Chapter 42 Disorders of Iron Metabolism
  • Chapter 43 Anemia Resulting from Other Nutritional Deficiencies
  • Chapter 44 Anemia Associated with Marrow Infiltration
  • Chapter 45 The Red Blood Cell Membrane and Its Disorders: Hereditary Spherocytosis, Elliptocytosis, and Related Diseases
  • Chapter 46 Disorders of Red Cells Resulting from Enzyme Abnormalities
  • Chapter 47 The Thalassemias: Disorders of Globin Synthesis
  • Chapter 48 Disorders of Hemoglobin Structure: Sickle Cell Anemia and Related Abnormalities
  • Chapter 49 Methemoglobinemia and Other Dyshemoglobinemias
  • Chapter 50 Hemolytic Anemia Resulting from Physical Injury to Red Cells
  • Chapter 51 Hemolytic Anemia Resulting from Chemical and Physical Agents
  • Chapter 52 Hemolytic Anemia Resulting from Infections with Microorganisms
  • Chapter 53 Hemolytic Anemia Resulting from Immune Injury
  • Chapter 54 Alloimmune Hemolytic Disease of the Fetus and Newborn
  • Chapter 55 Hypersplenism and Hyposplenism
  • Chapter 56 Primary and Secondary Polycythemias (Erythrocytosis)
  • Chapter 57 The Porphyrias
  • Chapter 58 Hereditary and Acquired Sideroblastic Anemias
Part VII. Neutrophils, Eosinophils, Basophils and Mast Cells
  • Chapter 59 Morphology of Neutrophils, Eosinophils, and Basophils
  • Chapter 60 Composition of Neutrophils
  • Chapter 61 Production, Distribution, and Fate of Neutrophils
  • Chapter 62 Eosinophils and Their Disorders
  • Chapter 63 Basophils and Mast Cells and Their Disorders
  • Chapter 64 Classification and Clinical Manifestations of Neutrophil Disorders
  • Chapter 65 Neutropenia and Neutrophilia
  • Chapter 66 Disorders of Neutrophil Function
Part VIII. Monocytes and Macrophages
  • Chapter 67 Morphology of Monocytes and Macrophages
  • Chapter 68 Biochemistry and Functions of Monocytes and Macrophages
  • Chapter 69 Production, Distribution, and Fate of Monocytes and Macrophages
  • Chapter 70 Classification and Clinical Manifestations of Disorders of Monocytes and Macrophages
  • Chapter 71 Monocytosis and Monocytopenia
  • Chapter 72 Inflammatory and Malignant Histiocytosis
  • Chapter 73 Lipid Storage Diseases
Part IX. Lymphocytes and Plasma Cells
  • Chapter 74 Morphology of Lymphocytes and Plasma Cells
  • Chapter 75 Composition and Biochemistry of Lymphocytes and Plasma Cells
  • Chapter 76 Lymphopoiesis
  • Chapter 77 Functions of B Lymphocytes and Plasma Cells in Immunoglobulin Production
  • Chapter 78 Functions of T Lymphocytes: T-Cell Receptors for Antigen
  • Chapter 79 Functions of Natural Killer Cells
  • Chapter 80 Classification and Clinical Manifestations of Lymphocyte and Plasma Cell Disorders
  • Chapter 81 Lymphocytosis and Lymphocytopenia
  • Chapter 82 Immunodeficiency Diseases
  • Chapter 83 Hematologic Manifestations of Acquired Immunodeficiency Syndrome
  • Chapter 84 Mononucleosis Syndromes
Part X. Neoplastic Myeloid Diseases
  • Chapter 85 Classification and Clinical Manifestations of the Clonal Myeloid Disorders
  • Chapter 86 Polycythemia Vera
  • Chapter 87 Essential Thrombocythemia
  • Chapter 88 Myelodysplastic Syndromes (Clonal Cytopenias and Oligoblastic Myelogenous Leukemia)
  • Chapter 89 Acute Myelogenous Leukemia
  • Chapter 90 Chronic Myelogenous Leukemia and Related Disorders
  • Chapter 91 Primary Myelofibrosis
Part XI. Neoplastic Lymphoid Diseases
  • Chapter 92 Classification of Malignant Lymphoid Disorders
  • Chapter 93 Acute Lymphoblastic Leukemia
  • Chapter 94 Chronic Lymphocytic Leukemia and Related Diseases
  • Chapter 95 Hairy Cell Leukemia
  • Chapter 96 Large Granular Lymphocytic Leukemia
  • Chapter 97 General Considerations of Lymphoma: Epidemiology, Etiology, Heterogeneity, and Primary Extranodal Disease
  • Chapter 98 Pathology of Malignant Lymphomas
  • Chapter 99 Hodgkin Lymphoma
  • Chapter 100 Diffuse Large B-Cell Lymphoma
  • Chapter 101 Follicular Lymphoma
  • Chapter 102 Mantle Cell Lymphoma
  • Chapter 103 Marginal Zone B-Cell Lymphomas
  • Chapter 104 Burkitt Lymphoma
  • Chapter 105 Cutaneous T-Cell Lymphoma (Mycosis Fungoides and Sézary Syndrome)
  • Chapter 106 Mature T-Cell and Natural Killer Cell Lymphomas
  • Chapter 107 Plasma Cell Neoplasms: General Considerations
  • Chapter 108 Essential Monoclonal Gammopathy
  • Chapter 109 Myeloma
  • Chapter 110 The Amyloidoses
  • Chapter 111 Macroglobulinemia
  • Chapter 112 Heavy-Chain Disease
Part XII. Hemostasis and Thrombosis
  • Chapter 113 Megakaryopoiesis and Thrombopoiesis
  • Chapter 114 Platelet Morphology, Biochemistry, and Function
  • Chapter 115 Molecular Biology and Biochemistry of the Coagulation Factors and Pathways of Hemostasis
  • Chapter 116 Control of Coagulation Reactions
  • Chapter 117 Vascular Function in Hemostasis
  • Chapter 118 Classification, Clinical Manifestations, and Evaluation of Disorders of Hemostasis
  • Chapter 119 Thrombocytopenia
  • Chapter 120 Reactive Thrombocytosis
  • Chapter 121 Hereditary Qualitative Platelet Disorders
  • Chapter 122 Acquired Qualitative Platelet Disorders
  • Chapter 123 The Vascular Purpuras
  • Chapter 124 Hemophilia A and Hemophilia B
  • Chapter 125 Inherited Deficiencies of Coagulation Factors II, V, VII, X, XI, and XIII and Combined Deficiencies of Factors V and VIII and of the Vitamin K-Dependent Factors
  • Chapter 126 Hereditary Fibrinogen Abnormalities
  • Chapter 127 von Willebrand Disease
  • Chapter 128 Antibody-Mediated Coagulation Factor Deficiencies
  • Chapter 129 Hemostatic Dysfunction Related to Liver Diseases and Liver Transplantation
  • Chapter 130 Disseminated Intravascular Coagulation
  • Chapter 131 Hereditary Thrombophilia
  • Chapter 132 The Antiphospholipid Syndrome
  • Chapter 133 Antibody-Mediated Thrombotic Disorders: Thrombotic Thrombocytopenic Purpura and Heparin-Induced Thrombocytopenia
  • Chapter 134 Venous Thrombosis
  • Chapter 135 Atherothrombosis: Disease Initiation, Progression, and Treatment
  • Chapter 136 Fibrinolysis and Thrombolysis
Part XIII. Transfusion Medicine
  • Chapter 137 Erythrocyte Antigens and Antibodies
  • Chapter 138 Human Leukocyte and Platelet Antigens
  • Chapter 139 Blood Procurement and Screening
  • Chapter 140 Red Cell Transfusion
  • Chapter 141 Preservation and Clinical Use of Platelets

    Book Details

    • Hardcover: 2460 pages
    • Publisher: McGraw-Hill Professional; 8 edition (July 9, 2010)
    • Language: English
    • ISBN-10: 0071621512
    • ISBN-13: 978-0071621519
    • Product Dimensions: 11 x 9 x 3 inches
    List Price: $275.00
     

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