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Williams Manual of Hematology, Eighth Edition

Williams Manual of Hematology, Eighth Edition

9780071622424
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Description

A convenient full-color reference distilled from the worlds leading hematology text – perfect when you need answers in the office, clinic, or on hospital rounds.

Williams Manual of Hematology, 8e is a concise and easy-to-navigate compilation of the pathogenic, diagnostic, and therapeutic essentials of blood cell and coagulation protein disorders. Referenced to the classic Williams Hematology, 8e, this handy, easily transported reference has been carefully edited to deliver only the most clinical point-of-care facts.

Covering both common and uncommon blood disorders, this complete guide includes sections on::

  • Disorders of red cells
  • Disorders of granulocytes
  • Disorders of monocytes and macrophages
  • The clonal myeloid disorders
  • The polyclonal lymphoid diseases
  • The clonal lymphoid and plasma cell diseases
  • Disorders of platelets and hemostasis
  • Disorders of coagulation proteins
  • Transfusion and hemapheresis

Now in full color for the first time, Williams Manual of Hematology, 8e is the fastest and most convenient way to access the unmatched clinical authority of Williams Hematology, 8e.

Product Details
McGraw Hill / Medical
49178
9780071622424
9780071622424

Data sheet

Publication date
2011
Issue number
8
Cover
paperback
Pages count
756
Dimensions (mm)
125 x 208
Weight (g)
637
  • Preface
    PART I:: INITIAL CLINICAL EVALUATION
    1. Approach to the Patient
    PART II:: DISORDERS OF RED CELLS
    2. Classification of Anemias and Polycythemias
    3. Aplastic Anemia:: Acquired and Inherited
    4. Pure Red Cell Aplasia
    5. Anemia of Chronic Renal Disease
    6. Anemia of Endocrine Disorders
    7. Congenital Dyserythropoietic Anemias
    8. The Megaloblastic Anemias
    9. Iron-Deficiency Anemia and Iron Overload
    10. Anemia Resulting from Other Nutritional Deficiencies
    11. Hereditary and Acquired Sideroblastic Anemias
    12. Anemia Resulting from Marrow Infiltration
    13. Anemia of Chronic Inflammation
    14. Hereditary Spherocytosis, Elliptocytosis, and Related Disorders
    15. Hemolytic Anemia Related to Red Cell Enzyme Defects
    16. The Thalassemias
    17. The Sickle Cell Diseases and Related Disorders
    18. Hemoglobinopathies Associated with Unstable Hemoglobin
    19. Methemoglobinemia and Other Dyshemoglobinemias
    20. Traumatic Hemolytic Anemia, March and Sports-Related Hemoglobinuria, and Traumatic Cardiac Hemolytic Anemia
    21. Microangiopathic Hemolytic Anemia
    22. Hemolytic Anemia Resulting from a Chemical or Physical Agent
    23. Hemolytic Anemia Resulting from Infectious Agents
    24. Hemolytic Anemia Resulting from Warm-Reacting Antibodies
    25. Cryopathic Hemolytic Anemia
    26. Drug-Induced Hemolytic Anemia
    27. Alloimmune Hemolytic Disease of the Newborn
    28. Hypersplenism and Hyposplenism
    29. Polyclonal Polycythemias (Primary and Secondary)
    30. The Porphyrias
    PART III:: DISORDERS OF GRANULOCYTES
    31. Classification and Clinical Manifestations of Neutrophil Disorders
    32. Neutrophenia and Neutrophilia
    33. Disorders of Neutrophil Functions
    34. Eosinophils and Their Diseases
    35. Basophils and Mast Cells and Their Diseases
    PART IV:: DISORDERS OF MONOCYTES AND MACROPHAGES
    36. Monocytosis and Monocytopenia
    37. Inflammatory and Malignant Histiocytosis
    38. Lipid Storage Disease
    PART V:: PRINCIPLES OF THERAPY FOR NEOPLASTIC HEMATOLOGICAL DISORDERS
    39. Pharmacology and Toxicity for Antineoplastic Drugs
    40. Principles of Hematopoietic Stem Cell Transplantation
    PART VI:: THE CLONAL MYELOID DISORDERS
    41. Classification and Clinical Manifestations of the Clonal Myeloid Disorders
    42. Myelodysplastic Syndromes (Clonal Cytopenias and Oligoblastic Myelogenous Leukemia)
    43. Polycythemia Vera
    44. Primary and Familial Thombocythemia
    45. Paroxysmal Nocturnal Hemoglobinuria (PNH)
    46. The Acute Myelogenous Leukemias
    47. The Chronic Myelogenous Leukemias
    48. Primary Myelofibrosis
    PART VII:: THE POLYCLONAL LYMPHOID DISEASES
    49. Classification of the Polyclonal Lymphoid Disorders
    50. Lymphocytosis and Lymphocytopenia
    51. Primary Immunodeficiency Syndrome
    52. The Acquired Immunodeficiency Syndrome
    53. The Mononucleosis Syndromes
    PART VIII:: THE CLONAL LYMPHOID AND PLASMA CELL DISEASES
    54. Classification and Clinical Manifestations of the Malignant Lymphoid Disorders
    55. The Acute Lymphocytic Leukemias
    56. The Chronic Lymphocytic Leukemias
    57. Hairy Cell Leukemias
    58. Large Granular Lymphocytic Leukemia
    59. Hodgkin Lymphoma
    60. General Considerations of Lymphoma:: Epidemiology, Etiology, Heterogeneity, and Primary Extranodal Disease
    61. Diffuse Large B-Cell Lymphoma
    62. Follicular Lymphomas
    63. Mantle Cell Lymphoma
    64. Marginal Zone-B-Cell Lymphoma
    65. Burkitt Lymphoma
    66. Cutaneous T-Cell Lymphoma (Mycosis Fungoides and Sezary Syndrome)
    67. Mature T-Cell and Natural Killer Cell Lymphomas
    68. Essential Monoclonal Gammopathy
    69. Myeloma
    70. Macroglobulinemia
    71. Heavy-Chain Diseases
    72. Amyloidosis
    PART IX:: DISORDERS OF PLATELETS AND HEMOSTATIS74. Thrombocytopenia
    75. Reactive (Secondary) Thrombocytosis
    76. Hereditary Platelet Disorders
    77. Acquired Platelet Disorders
    78. The Vascular Purpuras
    PART X:: DISORDERS OF COAGULATION PROTEINS
    79. Hemophilia A and B
    80. von Willebrand Disease
    81. Hereditary Disorders of Fibrinogen
    82. Inherited Deficiencies of Coagulation Factors II, V, VII, X, XI, and XIII and the Combined Deficiencies of Factors V and VIII and of the Vitamin K-Dependent Factors
    83. Antibody-Mediated Coagulation Factor Deficiencies
    84. Hemostatic Dysfunction Related to Liver Diseases
    85. The Antiphospholipid Syndrome (Lupus Anticoagulant and Related Disorders)
    86. Disseminated Intravascular Coagulation
    87. Fibrinolysis and Thrombolysis
    PART XI:: THROMBOSIS AND ANTITHROMBOTIC THERAPY
    88. Principles of Antithrombotic Therapy
    89. Hereditary Thrombophilia
    90. Venous Thromboembolism
    91. Antibody-Mediated Thrombotic Disorders:: Thrombotic Thrombocytopenic Purpura and Heparin-Induced Thrombocytopenia
    PART XII:: TRANSFUSION AND HEMAPHERESIS
    92. Red Cell Transfusion
    93. Transfusion of Platelets
    94. Therapeutic Hemapheresis
    Table of Normal Values
    Index
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