Williams manual of hematology

著者

書誌事項

Williams manual of hematology

McGraw-Hill Medical, c2011

8th ed. / [edited by] Marshall A. Lichtman ... [et al.]

  • : pbk

タイトル別名

Manual of hematology

大学図書館所蔵 件 / 全3件

この図書・雑誌をさがす

注記

Other editors: Kenneth Kaushansky, Thomas J. Kipps, Josef T. Prchal, Marcel M. Levi

Includes bibliographical references and index

内容説明・目次

内容説明

A convenient full-color reference distilled from the world's 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 cellsDisorders of granulocytesDisorders of monocytes and macrophagesThe clonal myeloid disordersThe polyclonal lymphoid diseasesThe clonal lymphoid and plasma cell diseasesDisorders of platelets and hemostasisDisorders of coagulation proteinsTransfusion 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.

目次

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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