Atnaujinkite slapukų nuostatas

Color Atlas of Clinical Hematology 3rd Revised edition [Kietas viršelis]

  • Formatas: Hardback, 352 pages, aukštis x plotis x storis: 189x246x38 mm, weight: 1935 g, 1600 ills.
  • Išleidimo metai: 22-May-2000
  • Leidėjas: Mosby
  • ISBN-10: 0723431159
  • ISBN-13: 9780723431152
Kitos knygos pagal šią temą:
  • Formatas: Hardback, 352 pages, aukštis x plotis x storis: 189x246x38 mm, weight: 1935 g, 1600 ills.
  • Išleidimo metai: 22-May-2000
  • Leidėjas: Mosby
  • ISBN-10: 0723431159
  • ISBN-13: 9780723431152
Kitos knygos pagal šią temą:
New edition of a classic reference in the field of hematology. This highly illustrated, color visual diagnostic aid brings together the clinical, morphological and investigational aspects of the whole range of blood disorders encountered by the clinician in everyday practice. The reproduction of photomicrographs are supported by succint, clinically-directed text and explanatory artworks and tables. In addition, this edition provides coverage on newly discovered cytokines, research into the mechanisms of action of thrombopoeitin, increase in the use of stem cell transplantation and cord blood transfusion, new leukemia types and classifications of lymphomas, and state-of-the-art blood transfusion techniques, including screening for newly discovered hepatitis viruses. Oversize: 10x12.5<"> Annotation c. Book News, Inc., Portland, OR (booknews.com)

This highly revised and updated atlas is the third edition of an essential reference in the field of hematology. Highly illustrated, this colorful visual diagnostic aid condenses the pathogenesis, clinical, morphological, and investigative aspects of the whole range of blood disorders into one, comprehensive resource. The detailed reproduction of photomicrographs, along with concise, clinically-directed text facilitates the recognition of morphological abnormalities in blood and bone marrow cells. The highly accessible format of this text enables quick and easy reference for anyone using it.
Preface iii
Normal Hemopoiesis and Blood Cells
1(40)
Hemopoietic stem and progenitor cells
1(1)
Adhesion molecules
2(1)
Hemopoietic growth factors
3(4)
Erythropoietin
6(1)
Thrombopoietin
6(1)
Lymbphokines and monokines
7(1)
Interleukin-1
7(1)
Interleukin-2
8(1)
Interleukin-4
8(1)
Interleukin-6
8(1)
Interleukin 7--15
8(1)
Apoptosis
8(1)
Interferons
9(1)
Tumor necrosis factor (α) and lymphotoxin (tumor necrosis factor β)
9(1)
Migration inhibition factor
9(1)
Membrane-growth factor interactions
9(4)
Growth factor receptors
9(1)
Signal transduction
10(2)
Transcription factors
12(1)
Cell cycle
12(1)
Oncogenes and tumor suppressor genes
13(1)
Chromosomes
14(1)
Telomeres
14(1)
Bone marrow examination
14(6)
Erythropoiesis
17(1)
Granulopoiesis and monocyte production
18(1)
Megakaryocyte and platelet production
19(1)
Lymphocytes and plasma cells
19(1)
Assessment of iron status
20(1)
Osteoblasts and osteoclasts
20(1)
Cells in mitosis
20(1)
Peripheral blood cells
20(4)
Red cells
24(1)
Granulocytes
25(1)
Neutrophils (polymorphs)
25(1)
Eosinophils
25(1)
Basophils
26(1)
Mononuclear phagocytic system
26(4)
Monocytes
26(1)
Reticuloendothelial system: phagocytes and dendritic cells
26(4)
Lymphocytes
30(9)
T cells
30(1)
B cells
31(3)
Natural killer cells
34(1)
Lymphocyte proliferation and differentiation
35(2)
Somatic hypermutation in normal B cells
37(1)
Lymphocyte circulation
37(2)
Mesenchymal cells
39(2)
Hypochromic anemias and Iron Overload
41(16)
Iron metabolism
41(1)
Iron-deficiency anemia
41(6)
Blood and bone marrow appearances
42(3)
Causes of iron deficiency
45(2)
Sideroblastic anemia
47(4)
Alcohol
51(1)
Lead poisoning
52(1)
Differential diagnosis of hypochromic microcytic anemias
52(1)
The porphyria
52(2)
Congenital erythropoietic porphyria
52(2)
Congenital erythropoietic protoporphyria
54(1)
Iron overload: primary (genetic) hemochromatosis
54(2)
Other causes of iron overload
56(1)
Hereditary hyperferritinemia with autosomal dominant congenital cataract syndrome
56(1)
Megaloblastic Anemias
57(14)
Clinical features
59(6)
Blood count and blood film appearances
61(1)
Bone marrow appearances
62(3)
Causes of megaloblastic anemia
65(5)
Vitamin B12 deficiency
65(2)
Folate deficiency
67(1)
Abnormalities of vitamin B12 or folate metabolism
67(2)
Other causes
69(1)
Treatment of megaloblastic anemia
70(1)
Causes of macrocytosis other than megaloblastic anemia
70(1)
Hemolytic Anemia
71(14)
Hereditary hemolytic anemia
73(6)
Normal red cell membrane
73(1)
Red cell blood group antigens
73(1)
Hereditary spherocytosis
74(1)
Hereditary elliptocytosis
74(1)
South-east Asian ovalocytosis (stomatocytic hereditary elliptocytosis)
74(2)
Other rare inherited defects of the red cell membrane
76(1)
Normal red cell metabolism
77(1)
Glucose 6-phosphate dehydrogenase deficiency
77(1)
Pyruvate kinase deficiency
78(1)
Pyrimidine 5-nucleotidase deficiency
78(1)
Acquired hemolytic anemia
79(6)
Autoimmune hemolytic anemias
79(2)
Drug-induced immune hemolytic anemia
81(1)
Isoimmune hemolytic anemia
81(1)
Red cell fragmentation syndromes
81(1)
Secondary hemolytic anemias
82(1)
Paroxysmal nocturnal hemoglobinuria
82(2)
Other hemolytic anemias
84(1)
Genetic Disorders of Hemoglobin
85(22)
Thalassemia
85(15)
β-Thalassemia major
87(7)
β-Thalassemia intermedia
94(2)
β-Thalassemia trait
96(1)
β-Thalassemia with a dominant phenotype
96(1)
Antenatal diagnosis
97(1)
α-Thalassemia
98(1)
X-Linked α-thalassemia and mental retardation syndrome
99(1)
The structural hemoglobin variants
100(7)
Sickle cell anemia
100(5)
Other structural hemoglobin defects
105(1)
F-cells
105(2)
Aplastic, Dyserythropoietic and Secondary Anemias
107(10)
Aplastic anemia
107(4)
Congenital aplastic anemia
107(1)
Bone marrow appearances
108(2)
Ferrokinetics
110(1)
Treatment
111(1)
Red cell aplasia
111(1)
Congenital dyserythropoietic anemias
112(2)
Secondary anemias
114(3)
Benign Disorders of Leukocytes
117(22)
Hereditary variation in white cell morphology
117(1)
Pelger-Huet anomaly
117(1)
May-Hegglin anomaly
117(1)
Chediak-Higashi syndrome
117(1)
Alder's (Alder--Reilly) anomaly
118(1)
Mucopolysaccharidoses VI and VII
118(1)
Other cause of lymphocyte vacuolation
118(1)
Disorders of phagocytic function
118(1)
Leucocytosis
118(2)
Neutrophil leucocytosis (neutrophilia)
118(2)
Eosinophil leucocytosis (eosinophilia)
120(1)
Monocytosis and basophil leucocytosis
120(1)
Leukemoid reaction
120(1)
Leucoerythroblastic reaction
121(1)
Neutropenia
121(3)
Kostmann's syndrome
122(1)
Shwachman-Diamond syndrome
122(1)
Clinical and bone marrow findings
122(1)
Felty's syndrome
123(1)
Histiocytic proliferations
124(2)
Lengerhan cell histiocytosis
124(1)
Hemophagocytic lymphohistiocytosis
125(1)
Sinus histiocytosis with massive lymphadenopathy
126(1)
Lymphocytosis
126(5)
Infectious mononucleosis
126(4)
Kikuchi's disease
130(1)
Primary immunodeficiency disorders
131(2)
Acquired immune deficiency syndrome
133(5)
Autoimmune lymphoproliferative syndrome
138(1)
Acute Leukemias
139(28)
Clinical features
140(5)
Microscopical appearances
145(7)
Acute myeloid leukemia
145(5)
Acute lymphoblastic leukemia
150(2)
Cytochemistry
152(2)
Immunological markers
154(4)
Electron microscopy
158(1)
Congenital acute leukemia
158(1)
Acute leukemia and Down syndrome
158(1)
Cytogenetics
158(4)
Minimal residual disease
162(2)
Management
164(2)
Acute myeloid leukemia
164(1)
Acute lymphoblastic leukemia
164(2)
Drug resistance
166(1)
Chronic Myeloid Leukemias and Myelodysplasia
167(10)
Chronic myeloid leukemia
167(5)
Clinical features
168(1)
Treatment
169(2)
Philadelphia-negative-chronic myeloid leukemia
171(1)
Myelodysplastic syndromes
172(4)
Monosomy 7 syndrome of childhood
176(1)
Myelokathexis
176(1)
Chronic lymphoid Leukemias
177(14)
Chronic B-cell leukemias
177(1)
Chronic Lymphocytic Leukemia
177(5)
Cytogenetics
180(1)
Apoptosis
180(1)
Membrane markers
180(1)
VH gene status
180(1)
Staging and treatment
180(1)
Chronic lymphocytic leukemia: mixed cell types
181(1)
Richter's syndrome (immunoblastic transformation)
182(1)
Prolymphocytic leukemia
182(1)
Hairy cell leukemia
183(2)
Hairy cell leukemia variant
185(1)
Plasma cell leukemia
185(1)
Leukemia--lymphoma syndromes
185(2)
Splenic lymphoma with villous lymphocytes
185(1)
Lymphoplasmacytic lymphoma
186(1)
Follicular lymphoma in leukemia phase
186(1)
Mantle cell lymphoma
186(1)
Large cell lymphoma
187(1)
Large granular lymphocytic leukemia (chronic T-cell lymphocytosis)
187(1)
T-Cell prolymphocytic leukemia
187(1)
Adult T-cell leukemia--lymphoma
188(2)
Sezary syndrome
190(1)
Malignant Lymphomas
191(56)
Non-Hodgkin Lymphomas
191(17)
Introduction
191(1)
Georgraphic variation, viruses, chromosomes and oncogenes
191(1)
Clinical features and diagnosis
192(4)
Morphological diagnosis
196(9)
Classification of lymphoma
205(1)
The Revised European--American Lymphoma (REAL) and World Health Organization [ WHO] schemes
205(3)
The World Health Organization classification
208(1)
B Cell non-Hodgkin lymphoma
208(7)
Precursor B cell acute lymphoblastic lymphoma/leukemia
208(1)
Small lymphocytic lymphoma and chronic lymphocytic leukemia
208(1)
Lymphoplasmacytic lymphoma (immunocytoma)
208(2)
Follicular lymphoma
210(1)
Mantle cell lymphoma
210(2)
Marginal zone lymphomas
212(1)
Hairy cell leukemia
213(1)
Burkitt's lymphoma
213(1)
Diffuse large B cell lymphoma
213(1)
Plasmacytoma and multiple myeloma
214(1)
Rare and provisional B cell entities
214(1)
T and NK cell neoplasms
215(6)
Precursor T cell acute lymphoblastic lymphoma and/or leukemia
215(1)
Chronic T cell chronic lymphocytic leukemia
215(1)
Large granular lymphocytic leukemia
215(1)
Mycosis fungoides and Sezary syndrome
215(1)
Peripheral T cell lymphoma, unspecified
216(2)
T/NK nasal-type (angiocentric) lymphoma
218(1)
Intestinal- and/or enteropathy-associated T cell lymphoma
218(2)
Other peripheral T cell lymphomas
220(1)
Angioimmunoblastic lymphadenopathy
220(1)
Adult T cell leukemia/lymphoma
220(1)
Anaplastic large cell lymphoma
220(1)
Treatment of non-Hodgkin lymphoma
221(2)
Low-grade tumors
222(1)
High-grade neoplasms
222(1)
Burkitt's lymphoma and lymphoblastic lymphoma
222(1)
Histological grading and prognostic markers
222(1)
Unclassified and reactive lymphoproliferative disorders
222(1)
True histiocytic lymphomas and other histiocytic proliferations
223(1)
Monocytic leukemia
223(1)
Hodgkin lymphoma (Hodgkin's disease)
223(10)
Presentation and evolution
223(4)
Classification of Hodgkin lymphoma
227(2)
Staging techniques
229(3)
Treatment
232(1)
Myeloma and Related Conditions
233(7)
Multiple myeloma
233(5)
Plasma cell leukemia
238(1)
Treatment
238(2)
Primary amyloidosis
240(1)
Other plasma cell tumors
240(2)
Solitary plasmacytoma of bone
241(1)
Soft tissue plasmacytoma
241(1)
Waldenstrom's macroglobulinemia
242(2)
Other causes of serum M-proteins
244(3)
Benign monoclonal gammopathy
244(1)
Cryoglobulinemia
244(1)
Heavy chain diseases
245(2)
Non-Leukemic Myeloproliferative Disorders
247(12)
Polycythemia vera
247(3)
Myelofibrosis
250(4)
Essential thrombocythemia
254(3)
Leukemic transformation of polycythemia vera and myelofibrosis
257(1)
Acute myelofibrosis
258(1)
Stem Cell Transplantation
259(8)
Steam cell transplantation
259(2)
Low intensity conditioning (LIC)-transplants
261(1)
Donor leucocytes
261(1)
Complications of stem cell transplants
261(6)
Graft-versus-host disease
264(3)
Vascular and Platelet Bleeding Disorders
267(12)
Hemostasis and bleeding disorders
267(1)
Vascular bleeding disorders
268(4)
Hereditary hemorrhagic telangiectasia
269(1)
Ehlers--Danlos syndrome
269(1)
Senile purpura
269(1)
Scurvy
269(1)
Purpura associated with abnormal proteins
270(1)
Allergic purpuras
270(1)
Pupura associated with infection
270(2)
Platelet bleeding disorders
272(7)
Thrombocytopenia
272(4)
Disorders of platelet function
276(3)
Coagulation Disorders
279(18)
The coagulation pathway
279(1)
Hereditary coagulation disorders
279(8)
Hemophilia
279(5)
Carrier detection and diagnosis
284(1)
Von Willebrand's disease
284(3)
Other hereditary coagulation disorders
287(1)
Acquired coagulation disorders
287(3)
Liver disease
287(1)
Overdosage with anticoagulants
287(1)
Disseminated intravascular coagulation
288(1)
Acquired coagulation factor inhibitor
288(2)
Thrombophilia
290(2)
Inherited thrombotic disorders
290(2)
Acquired thrombotic risk factors
292(1)
Diagnosis of venous thrombosis
292(2)
Antithrombotic therapy
294(3)
Heparin
294(1)
Oral anticoagulants
294(1)
Thrombin inhibitors
294(2)
Fibrinolytic agents
296(1)
Bone Marrow in Non-Hemopoietic Diseases
297(16)
Metastatic bone tumors
297(3)
Mast cell disease
300(1)
Granulomatous disease
300(2)
Sarcoidosis
300(2)
Tuberculosis
302(1)
Other granulomas
302(1)
Kala-azar (visceral leishmaniasis)
302(1)
Other infections
303(1)
Lysosomal storage diseases
303(4)
Gaucher's disease
303(3)
Niemann--Pick disease
306(1)
Sea-blue histiocyte syndrome
306(1)
Cystinosis
307(1)
Primary oxaluria
307(1)
Osteopetrosis (Albers--Schonberg or marble bone disease)
307(1)
Amyloidosis
308(2)
Renal asteodystrophy and osteomalacia
310(1)
Paget's disease of bone (osteitis deformans)
310(1)
Anorexia nervosa
311(1)
Systemic lupus erythematosus
312(1)
Magnetic resonance imaging of bone marrow
312(1)
Parasitic Infections Diagnosed in Blood
313(8)
Malaria
313(4)
Effect of malaria on various organs
315(1)
Comparative methods for malaria diagnosis
316(1)
Toxoplasmosis
317(1)
Babesiosis
317(1)
Trypanosomiasis
318(1)
Bancroftian filariasis
318(1)
Loiasis
318(1)
Bartonellosis
319(1)
Relapsing fever
320(1)
Blood Transfusion
321(14)
Blood transfusion
321(5)
Red cell antigens
321(1)
Red cell antibodies
322(1)
ABO system
322(1)
Rh system
322(1)
Blood grouping and cross-matching
323(1)
Red cell components
324(1)
Clinical blood transfusion
324(2)
Complications of blood transfusions
326(2)
Infections
326(1)
Prion disease
326(2)
Iron overload
328(1)
Transfusion-related acute lung injury
328(1)
Graft-versus-host disease
328(1)
Other blood components
328(2)
Platelet concentrates
329(1)
Leucocytes
329(1)
Plasma components
329(1)
Human leucocyte antigen system
330(2)
Human leucocyte antigen nomenclature
330(2)
Typing of human leucocyte antigens
332(1)
Other human leucocyte antigens
332(3)
Appendix 1 335(4)
Appendix 2 339(1)
Index 340