Williams Manual of Hematology, Eighth Edition

by Lichtman, Marshall A.

• ISBN13: 9780071622424
• ISBN10: 007162242X
• Edition: 8th
• Format: Paperback
• Copyright: 2011-05-31
• Publisher: McGraw-Hill Education / Medical

Summary

A quick reference distilled from the world's leading hematology text -- perfect when you need on-the-spot answers on rounds or in the clinic New full-color presentation! Edited by the leading figures in global hematology and distilled from the classic Williams Hematology, 8e, this is the fasted and most convenient way for students, residents, fellows, and clincians to access authoritative information on more than 100 hematologic diseases and their management. Features: NEW full-color design includes images of blood and clinical specimans conveniently appearing near the descriptive text EXANDED COVERAGE of all the lymphomas, genetics and genomics, NEW coverage of frontline therapies, EXPANDED coverage of targeted and monocional therapies for hematological disease Carefully edited to present only the most clinical, point-of-care facts

Table of Contents

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