Williams血液学（第9版）(英文版）

　　简  目
　　Contributors
　　Preface
　　PART IClinical Evaluation of the Patient
　　PARTII  TheOrganization of the LymphohematopoieticTissues
　　PARTIII  EpochalHematology
　　PARTIV  Molecular and CellularHematology
　　PARTV  TherapeuticPrinciples
　　PARTVI  The Erythrocyte
　　PARTVII  Neutrophils,Eosinophils,Basophils, and Mast Cells
　　PARTVIII  Monocytes and Macrophages
　　PARTIX  Lymphocytes and Plasma Cells
　　PARTX  MalignantMyeloid Diseases
　　PARTXI  MalignantLymphoid Diseases
　　PARTXII  Hemostasis andThrombosis
　　PARTXIII  Transfusion Medicine
　　Index
　　 
　　 
　　 
　　v 
　　 
　　 
　　目  录
　　Contributors. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .ix
　　Preface. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .xxi
　　 
　　PART I
　　ClinicalEvaluation of the Patient
　　1.InitialApproachto the Patient:HistoryandPhysicalExamination
　　2.Examinationof Blood Cells
　　3.ExaminationofTheMarrow
　　4.ConsultativeHematology
　　PART II
　　TheOrganization of the LymphohematopoieticTissues
　　5.Structureof the Marrowand the HematopoieticMicroenvironment
　　6.The Organization and StructureofLymphoid Tissues
　　PART III
　　Epochal Hematology
　　7.Hematologyof the FetusandNewborn
　　8.HematologyduringPregnancy
　　9.Hematology in OlderPersons
　　 
　　PART IV
　　Molecular and CellularHematology
　　10.Genetic PrinciplesandMolecular Biology
　　11.Genomics
　　12.Epigenetics
　　13.Cytogeneticsand Genetic Abnormalities
　　14.MetabolismofHematologicNeoplastic Cells
　　15.ApoptosisMechanisms:Relevanceto the HematopoieticSystem
　　16.Cell-CycleRegulationandHematologicDisorders
　　17.SignalTransductionPathways
　　18.HematopoieticStem Cells, Progenitors,andCytokines
　　19.TheInflammatory Response
　　20.InnateImmunity
　　21.Dendritic Cells andAdaptiveImmunity
　　PARTV
　　TherapeuticPrinciples
　　22.PharmacologyandToxicityofAntineoplastic Drugs
　　23.Hematopoietic Cell Transplantation
　　24.Treatment of InfectionsinTheImmunocompromisedHost
　　25.AntithromboticTherapy
　　26.Immune Cell Therapy
　　27.VaccineTherapy
　　28.TherapeuticApheresis:Indications,Efficacy,andComplications
　　29.Gene TherapyforHematologicDiseases
　　30.RegenerativeMedicine:MultipotentialCellTherapy for
　　TissueRepair
　　PARTVI
　　The Erythrocyte
　　31.StructureandCompositionof the Erythrocyte
　　32.Erythropoiesis
　　33.Erythrocyte Turnover
　　34.ClinicalManifestations and Classification ofErythrocyteDisorders
　　35.AplasticAnemia:Acquiredand Inherited.
　　36. Pure Red Cell Aplasia
　　37.  Anemia of ChronicDisease
　　38.  The Congenital DyserythropoieticAnemias
　　39.  Paroxysmal Nocturnal Hemoglobinuria
　　40.  ParoxysmalNocturnalHemoglobinuria
　　41.  Folate,Cobalamin,andMegaloblasticAnemias
　　42.IronMetabolism
　　43.Iron Deficiency andOverload
　　44.  Anemia Resulting fromOtherNutritionalDeficiencies
　　45.  Anemia AssociatedwithMarrowInfiltration
　　46.  Erythrocyte MembraneDisorders
　　47.  Erythrocyte Enzyme Disorders
　　48.  TheThalassemias: Disorders of GlobinSynthesis
　　49.  DisordersofHemoglobinStructure:Sickle CellAnemiaandRelatedAbnormalities
　　50.  Methemoglobinemiaand Other Dyshemoglobinemias
　　51.  FragmentationHemolyticAnemia
　　52.  Erythrocyte Disordersas a ResultofChemicalandPhysicalAgents
　　53.  HemolyticAnemiaResultingfromInfectionswithMicroorganisms
　　54.  HemolyticAnemiaResultingfromImmuneInjury
　　55.  AlloimmuneHemolytic Disease of the FetusandNewborn
　　56.  HypersplenismandHyposplenism
　　57.  Primary and Secondary Erythrocytoses
　　58.ThePorphyrias
　　59.PolyclonalandHereditarySideroblasticAnemias
　　PARTVII
　　Neutrophils,Eosinophils,Basophils, and Mast Cells
　　60. StructureandCompositionofNeutrophils,Eosinophils,andBasophils
　　61. Production,Distribution,andFateofNeutrophils
　　62. EosinophilsandRelatedDisorders
　　63. Basophils,Mast Cells, andRelatedDisorders
　　64. Classificationand Clinical ManifestationsofNeutrophilDisorders
　　65. NeutropeniaandNeutrophilia
　　66. DisordersofNeutrophilFunction
　　PARTVIII
　　Monocytes and Macrophages
　　67. Structure,Receptors,andFunctionsofMonocytesandMacrophages
　　68. Production,Distribution,andActivationofMonocytesandMacrophages
　　69. Classificationand ClinicalManifestationsof DisordersofMonocytesandMacrophages
　　70. MonocytosisandMonocytopenia
　　71. Inflammatory andMalignantHistiocytosis
　　72.  Gaucher Disease andRelatedLysosomalStorageDiseases
　　73.  PART IX
　　Lymphocytes and Plasma Cells
　　73.The StructureofLymphocytes andPlasma Cells
　　74.LymphopoiesisFunctionsof B LymphocytesandPlasma Cells inImmunoglobulinProduction
　　75.  Functionsof T Lymphocytes:T-CellReceptorsforAntigen
　　76.  FunctionsofNaturalKiller Cells
　　77.  Classificationand Clinical ManifestationsofLymphocyteandPlasma Cell Disorders
　　79.LymphocytosisandLymphocytopenia
　　80.Immunodeficiency Diseases
　　81.HematologicManifestationsofAcquiredImmunodeficiencySyndrome
　　82.MononucleosisSyndromes
　　PART X
　　MalignantMyeloid Diseases
　　83.Classification and ClinicalManifestationsoftheClonalMyeloidDisorders
　　84.PolycythemiaVera
　　85.EssentialThrombocythemia
　　86.Primary Myelofibrosis
　　87.MyelodysplasticSyndromes
　　88.AcuteMyelogenousLeukemia
　　89.ChronicMyelogenousLeukemiaandRelatedDisorders
　　PART XI
　　MalignantLymphoid Diseases
　　90.ClassificationofMalignantLymphoid Disorders
　　91.AcuteLymphoblasticLeukemia
　　92.ChronicLymphocyticLeukemia
　　93.Hairy Cell Leukemia
　　94.LargeGranularLymphocyticLeukemia
　　95.General ConsiderationsforLymphomas:Epidemiology,Etiology,Heterogeneity,and Primary Extranodal Disease
　　96.PathologyofLymphomas.
　　97.HodgkinLymphoma
　　98.Diffuse Large B-Cell Lymphoma andRelated Diseases
　　99.FollicularLymphoma
　　100.Mantle Cell Lymphoma
　　101.MarginalZone B-Cell Lymphomas
　　102.BurkittLymphoma
　　103.CutaneousT-CellLymphoma(MycosisFungoidesandSézarySyndrome)
　　104.MatureT-CellandNaturalKiller Cell Lymphomas
　　105.Plasma Cell Neoplasms: General Considerations
　　106.EssentialMonoclonalGammopathy
　　107.Myeloma.
　　108.ImmunoglobulinLight-ChainAmyloidosis
　　109.Macroglobulinemia.
　　110.Heavy-Chain Disease
　　PART XII
　　Hemostasis andThrombosis
　　111.Megakaryopoiesis andThrombopoiesis
　　112.PlateletMorphology,Biochemistry,and Function
　　113.Molecular Biology andBiochemistryof theCoagulationFactorsandPathwaysofHemostasis
　　114.ControlofCoagulationReactions
　　115.VascularFunction in Hemostasis
　　116.Classification, Clinical Manifestations, andEvaluationofDisordersofHemostasis
　　117.Thrombocytopenia
　　118.Heparin-Induced Thrombocytopenia
　　119.ReactiveThrombocytosis
　　120.HereditaryQualitativePlateletDisorders
　　121.AcquiredQualitativePlateletDisorders
　　122.TheVascularPurpuras
　　123. Hemophilia A andHemophilia B
　　124. InheritedDeficiencies of Coagulation FactorsII,V,V VIII, VII, X, XI, and XII
　　125. Hereditary Fibrinogen Abnormalities
　　126. von Willebrand Disease
　　127. Antibody-Mediated Coagulation FactorDeficiencies
　　128. HemostaticAlterations in Liver Disease andLiverTransplantation
　　129. DisseminatedIntravascularCoagulation
　　130.HereditaryThrombophilia
　　131. The AntiphospholipidSyndrome
　　132. Thrombotic Microangiopathies
　　133.VenousThrombosis
　　134. Atherothrombosis: Disease Initiation,Progression,andTreatment
　　135. Fibrinolysis andThrombolysis
　　PART XIII
　　Transfusion Medicine
　　136. Erythrocyte AntigensandAntibodies
　　137. Human Leukocyte andPlateletAntigens
　　138. Blood Procurementand Red Cell Transfusion
　　139. Preservationand Clinical UseofPlatelets
　　Index

　　考杉斯基(Kaushansky)博士是纽约州立大学石溪分校健康科学院的高级副总裁，同时担任该校医学院院长的职务。考杉斯基(Kaushansky)博士是全球知名的血液学专家，发表过多篇有影响力的著作。担任《Willians血液学》第8版、第9版的主编。

　　《Williams血液学》是血液学领域的经典之作，涵盖了血液学的所有方面，介绍了患者临床评估、血液病的分子学和细胞学基础，并具体阐述了红细胞疾病、粒细胞和单核细胞疾病、淋巴细胞和浆细胞疾病、髓系肿瘤性疾病、淋巴组织疾病、止血和血栓、输血医学等内容。第9版在第8版的基础上做了大篇幅的修改和更新，以反映血液学领域的*进展。新增加了表观遗传学和基因组学、血液肿瘤细胞的新陈代谢和肝素诱导性血小板减少症等内容。本书是血液科临床医生、实习生、血液学研究人员必不可少的案头佳作，也是学习血液学专业英语的工具书。