Williams Manual of Hematology, Tenth Edition

Cover
Title Page
Copyright Page
Contents
Preface
Part I. Initial Clinical Evaluation
	1. Approach to the Patient
Part II. Disorders of Red Cells
	2. Classification of Anemias and Erythrocytoses
	3. Aplastic Anemia: Acquired and Inherited
	4. Pure Red Cell Aplasia
	5. Anemia of Chronic (Inflammatory, Neoplastic, and Renal) Disease
	6. Erythropoietic Effects of Endocrine Disorders
	7. Congenital Dyserythropoietic Anemias
	8. Folate, Cobalamin, and Megaloblastic Anemias
	9. Iron Deficiency and Iron Overload
	10. Anemia Resulting from Other Nutritional Deficiencies
	11. Hereditary and Acquired Sideroblastic Anemias
	12. Anemia Resulting from Marrow Infiltration
	13. Erythrocyte Membrane Disorders
	14. Hemolytic Anemia Related to Red Cell Enzyme Defects
	15. The Thalassemias
	16. The Sickle Cell Diseases and Other Hemoglobinopathies
	17. Unstable Hemoglobins and Hemoglobins with Altered Oxygen Affinity
	18. Methemoglobinemia and Other Dyshemoglobinemias
	19. Fragmentation Hemolytic Anemia
	20. Hemolytic Anemia Resulting from a Chemical or Physical Agent
	21. Hemolytic Anemia Resulting from Infectious Agents
	22. Hemolytic Anemia Resulting from Warm-Reacting Antibodies
	23. Cryopathic Hemolytic Anemia
	24. Drug-Induced Hemolytic Anemia
	25. Alloimmune Hemolytic Disease of the Newborn
	26. Hypersplenism and Hyposplenism
	27. Polyclonal Erythrocytoses (Primary and Secondary)
	28. The Porphyrias
Part III. Disorders of Granulocytes
	29. Classification and Clinical Manifestations of Neutrophil Disorders
	30. Neutropenia and Neutrophilia
	31. Disorders of Neutrophil Function
	32. Eosinophils and Their Disorders
	33. Basophils, Mast Cells and Their Disorders
Part IV. Disorders of Monocytes and Macrophages
	34. Classification and Clinical Manifestations of Monocyte and Macrophage Disorders
	35. Monocytosis and Monocytopenia
	36. Inflammatory and Malignant Histiocytosis
	37. Gaucher Disease and Related Lysosomal Storage Diseases
Part V. Principles of Therapy for Neoplastic Hematologic Disorders
	38. Pharmacology and Toxicity of Antineoplastic Drugs
	39. Principles of Hematopoietic Cell Transplantation
	40. Immune Cell Therapy: Genetically Engineered T Cells
Part VI. The Clonal Myeloid Disorders
	41. Classification and Clinical Manifestations of the Clonal Myeloid Disorders
	42. Polycythemia Vera
	43. Essential Thrombocythemia
	44. Paroxysmal Nocturnal Hemoglobinuria
	45. Myelodysplastic Syndromes
	46. The Acute Myelogenous Leukemias
	47. The Chronic Myelogenous Leukemias
	48. Primary Myelofibrosis
Part VII. The Polyclonal Lymphoid Diseases
	49. Classification and Clinical Manifestations of Polyclonal Lymphocyte and Plasma Cell Disorders
	50. Lymphocytosis and Lymphocytopenia
	51. Primary Immunodeficiency Syndrome
	52. Hematologic Manifestations of the Acquired Immunodeficiency Syndrome
	53. The Mononucleosis Syndromes
Part VIII. The Clonal Lymphoid and Plasma Cell Diseases
	54. Classification and Clinical Manifestations of the Neoplastic Lymphocytic Disorders
	55. The Acute Lymphoblastic Leukemias
	56. The Chronic Lymphocytic Leukemias
	57. Hairy Cell Leukemia
	58. Large Granular Lymphocytic Leukemia
	59. General Considerations of Lymphoma: Epidemiology, Etiology, Heterogeneity, and Primary Extranodal Disease
	60. Hodgkin Lymphoma
	61. Diffuse Large B-Cell Lymphoma and Related Diseases
	62. Follicular Lymphoma
	63. Mantle Cell Lymphoma
	64. Marginal Zone B-Cell Lymphoma
	65. Burkitt Lymphoma
	66. Cutaneous T-Cell Lymphoma
	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 Hemostasis
	73. Clinical Manifestations, Evaluation and Classification of Disorders of Hemostasis
	74. Thrombocytopenia
	75. Hereditary and 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 Combined Deficiencies of Factor V and VIII and of Vitamin K–Dependent Factors
	83. Antibody-Mediated Coagulation Factor Deficiencies
	84. Hemostatic Dysfunction Related to Liver Diseases
	85. The Antiphospholipid Syndrome
	86. Disseminated Intravascular Coagulation
	87. Fibrinolysis and Thrombolysis
Part XI. Thrombosis and Antithrombotic Therapy
	88. Principles of Antithrombotic and Antifibrinolytic 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. Plasma and Plasma Component Therapy
	95. Therapeutic Hemapheresis
Table of Normal Values
Index