Williams Manual of Hematology
(Sprache: Englisch)
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...
Williams Manual of Hematology, 8e is a concise and easy-to-navigate compilation of the...
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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 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 thefastest and most convenient way to access the unmatched clinical authority of Williams Hematology, 8e.
Inhaltsverzeichnis zu „Williams Manual of Hematology “
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
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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 HEMOSTATIS 73. Clinical Manifestations, Evaluation, and Classification of Disorders of Hemostatis 74. 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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Autoren-Porträt von Marshall A. Lichtman
Marshall A. Lichtman, MDProfessor of Medicine and of Biochemistry and Biophysics
University of Rochester Medical Center
Rochester, NY
Kenneth Kaushansky, MD
Senior Vice President, Health Sciences
Dean, School of Medicine
Stony Brook University
Stony Brook, NY
Thomas J. Kipps, MD, PhD
Evelyn and Edwin Tasch Chair in Cancer Research
Professor of Medicine
Division of Hematology/Oncology
Deputy Director for Research Operations
Moores UCSD Cancer Center
University of California, San Diego
La Jolla, CA
Josef T. Prchal, MD
Professor of Medicine, Pathology, and Genetics
Hematology Division
University of Utah
Salt Lake City, UT
Department of Pathophysiology
First Faculty of Medicine
Charles University of Prague
Czech Republic
Marcel M. Levi, MD, PhD
Chairman, Department of Medicine
Academic Medical Center
University of Amsterdam
The Netherlands
Bibliographische Angaben
- Autor: Marshall A. Lichtman
- 2011, 8th ed., 756 Seiten, Maße: 16,9 x 21,1 cm, Kartoniert (TB), Englisch
- With Marshall A. Lichtman, Kenneth Kaushansky, Thomas J. Kipps et al.
- Verlag: McGraw-Hill Professional
- ISBN-10: 007162242X
- ISBN-13: 9780071622424
Sprache:
Englisch
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