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Haematology at a Glance, 4ed

Following the familiar, easy-to-use at a Glance format, Haematology at a Glance, Fourth Edition is a broad and accessible introduction to the study of blood. Fully revised and updated to reflect advances in the field and in clinical practice, this new edition covers essential knowledge, from basic hematological physiology to blood disorders and their diagnosis and treatment.

This new edition of Haematology at a Glance:

• Features expanded sections on the underlying mechanisms, diagnostic techniques and management of the malignant haematological diseases. Also incorporates recent advances in knowledge of thrombosis and the newer oral anticoagulants
• Contains the very latest clinical treatments
• Includes updated illustrations and clinical photographs to illustrate concepts and aid understanding
• Features extensive online self-assessment at www.ataglanceseries.com/haematology

This book is an invaluable resource for medical students and health professionals wanting to consolidate and expand their knowledge of haematology.

Review

Contents

۱. Haemopoiesis. physiology and pathology
۲. Normal blood cellsI. red cells
۳. Normal blood cells II. granulocytesr monocytes and the reticuloendothelial system
۴. Normal blood cells III. lymphocytes
۵. Lymph nodes, the lymphatic system and the spleen
۶. Clinical assessment
۷. Laboratory assessment
۸. General aspects of anaemia
۹. IronI. physiology and deficiency
۱۰. Iron II. overload and sideroblastic anaemia
۱۱. Megaloblastic anaemiaI. vitamin B12 (B12) and folate deficiency- biochemical basis, causes
۱۲. Megaloblastic anaemia II. clinical features, treatment and other macrocytic anaemias
۱۳. Haemolytic anaemiasI. general
۱۴. Haemolytic anaemias II. inherited membrane and enzyme defects
۱۵. Haemolytic anaemias III. acquired
۱۴. Red cell disorders
۱۶. Haemolytic anaemias IV. genetic defects of haemoglobin- thalassaemia
۱۷. Haemolytic anaemias V. genetic defects of haemoglobin – sickle cell disease
۱۸. Benign disorders of white cellsI. granulocytes, monocytesr macrophages
۱۹. Benign disorders of white cells II. lymphocytesr lymph nodes, spleen, HIV
۲۰. Introduction to haematological malignancy. basic mechanisms
۲۱. General aspects of treatment
۲۲. Acute leukaemiaI. classification and diagnosis
۲۳. Acute leukaemia II. treatment and prognosis
۲۴. Chronic myeloid leukaemia (BCR-ABL1 positive]
۲۵. Myelodysplasia (myelodysplastic syndromes)
۲۶. Myeloproliferative disordersI. introduction
۲۷. Myeloproliferative disorders II. polycythaemia rubra vera
۲۸. Myeloproliferative disorders III. essential thrombocythaemia, primary myelofibrosis and systemic mastocytosis
۲۹. Chronic lymphocytic leukaemia
۳۰. Multiple myeloma and plasma cell disorders
۳۱. LymphomaI. introduction
۳۲. Lymphoma II. Hodgkin lymphoma
۳۳. Lymphoma III. non-Hodgkin lymphoma – aetiology and classification
۳۴. Lymphoma IV. clinical and laboratory features of more common subtypes
۳۵. Lymphoma V. treatment and prognosis
۳۶. Bone marrow failure
۳۷. Haematological effects of drugs
۳۸. Stem cell transplantation
۳۹. Normal haemostasisI. vessel wall and platelets
۴۰. Normal haemostasis II. coagulation factors and fibrinolysis
۴۱. Disorders of haemostasisI. vessel ‘wall and platelets
۴۲. Disorders of haemostasis II. inherited disorders of coagulation
۴۳. Disorders of haemostasis III. acquired disorders of coagulation
۴۴. Thrombosis and antithrombotic therapy
۴۵. Anticoagulation
۴۶. Haematological aspects of tropical diseases
۴۷. Haematology of pregnancy and infancy
۴۸. Blood transfusionI
۴۹. Blood transfusion II