Haematology and the Asian Patient: 51 Clinical Cases
Autor Anskar Y.H. Leung, Edmond S K Maen Limba Engleză Paperback – 27 iun 2024
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Specificații
ISBN-13: 9781032351254
ISBN-10: 103235125X
Pagini: 248
Ilustrații: 110
Dimensiuni: 178 x 254 x 16 mm
Greutate: 0.46 kg
Ediția:1
Editura: CRC Press
Colecția CRC Press
Locul publicării:Boca Raton, United States
ISBN-10: 103235125X
Pagini: 248
Ilustrații: 110
Dimensiuni: 178 x 254 x 16 mm
Greutate: 0.46 kg
Ediția:1
Editura: CRC Press
Colecția CRC Press
Locul publicării:Boca Raton, United States
Public țintă
ProfessionalCuprins
About the editors
Haemostasis and Thrombosis
1 Von Willebrand Disease. 2 Severe Haemophilia. 3 Factor VII Deficiency. 4 Acquired haemophilia. 5 Acquired Factor V Inhibitor. 6 Disseminated Intravascular Coagulopathy. 7 Cancer-related Thrombosis.
Myeloid Malignancy
8 Acute Myeloid Leukaemia I. 9 Acute Myeloid Leukaemia II. 10 Myelodysplastic Syndrome. 11 Chronic Myeloid Leukaemia. 12 Essential Thrombocytosis. 13 Polycythemia Vera. 14 Primary Myelofibrosis. 15 Myeloid Neoplasm with Germline Predisposition. 16 Langerhans Cell Histiocytosis.
Lymphoid Malignancy
17 Diffuse Large B-Cell Lymphoma. 18 Waldenström Macroglobulinaemia. 19 Chronic Lymphocytic Leukaemia. 20 Hairy Cell Leukaemia. 21 Philadelphia Chromosome-Positive Acute Lymphoblastic Leukaemia. 22 Natural Killer Cell Lymphoma. 23 Mycosis Fungoides. 24 T-cell Prolymphocytic Leukaemia. 25 Hodgkin Lymphoma.
Plasma Cell Neoplasms
26 Amyloidosis. 27 Multiple Myeloma. 28 POEMS Syndrome.
Thalassaemia and Haemoglobin Disorders
29 β-Thalassaemia Major. 30 Haemoglobin H Disease. 31 Sickle Cell Disease. 32 Methaemogloblinaemia.
Nutritional and Aplastic Anaemia
33 Aplastic Anaemia. 34 Iron Deficiency Anaemia. 35 Vitamin B12-Deficiency Anaemia.
Haemolytic Anaemia
36 Warm-type Autoimmune Haemolytic Anaemia. 37 Cold Agglutinin Disease. 38 G6PD Deficiency. 39 Hereditary Spherocytosis. 40 Paravalvular Leak. 41 Paroxysmal Nocturnal Haemoglobinuria. 42 Thrombotic Thrombocytopenic Purpura. 43 Atypical Haemolytic Uraemic Syndrome.
Thrombocytopenia
44 Immune Thrombocytopenia. 45 Hereditary Macrothrombocytopenia
Miscellaneous Conditions
46 Castleman Disease. 47 Haemophagocytic Lymphohistiocytosis. 48 Hypereosinophilia. 49 IgG4-related Disease. 50 Lymphadenopathy and Hypergammaglobulinaemia. 51 Paraneoplastic Pemphigus.
Index
Haemostasis and Thrombosis
1 Von Willebrand Disease. 2 Severe Haemophilia. 3 Factor VII Deficiency. 4 Acquired haemophilia. 5 Acquired Factor V Inhibitor. 6 Disseminated Intravascular Coagulopathy. 7 Cancer-related Thrombosis.
Myeloid Malignancy
8 Acute Myeloid Leukaemia I. 9 Acute Myeloid Leukaemia II. 10 Myelodysplastic Syndrome. 11 Chronic Myeloid Leukaemia. 12 Essential Thrombocytosis. 13 Polycythemia Vera. 14 Primary Myelofibrosis. 15 Myeloid Neoplasm with Germline Predisposition. 16 Langerhans Cell Histiocytosis.
Lymphoid Malignancy
17 Diffuse Large B-Cell Lymphoma. 18 Waldenström Macroglobulinaemia. 19 Chronic Lymphocytic Leukaemia. 20 Hairy Cell Leukaemia. 21 Philadelphia Chromosome-Positive Acute Lymphoblastic Leukaemia. 22 Natural Killer Cell Lymphoma. 23 Mycosis Fungoides. 24 T-cell Prolymphocytic Leukaemia. 25 Hodgkin Lymphoma.
Plasma Cell Neoplasms
26 Amyloidosis. 27 Multiple Myeloma. 28 POEMS Syndrome.
Thalassaemia and Haemoglobin Disorders
29 β-Thalassaemia Major. 30 Haemoglobin H Disease. 31 Sickle Cell Disease. 32 Methaemogloblinaemia.
Nutritional and Aplastic Anaemia
33 Aplastic Anaemia. 34 Iron Deficiency Anaemia. 35 Vitamin B12-Deficiency Anaemia.
Haemolytic Anaemia
36 Warm-type Autoimmune Haemolytic Anaemia. 37 Cold Agglutinin Disease. 38 G6PD Deficiency. 39 Hereditary Spherocytosis. 40 Paravalvular Leak. 41 Paroxysmal Nocturnal Haemoglobinuria. 42 Thrombotic Thrombocytopenic Purpura. 43 Atypical Haemolytic Uraemic Syndrome.
Thrombocytopenia
44 Immune Thrombocytopenia. 45 Hereditary Macrothrombocytopenia
Miscellaneous Conditions
46 Castleman Disease. 47 Haemophagocytic Lymphohistiocytosis. 48 Hypereosinophilia. 49 IgG4-related Disease. 50 Lymphadenopathy and Hypergammaglobulinaemia. 51 Paraneoplastic Pemphigus.
Index
Notă biografică
Professor Anskar Leung is currently Chair Professor of Haematology and Deputy Chairperson in the Department of Medicine at the University of Hong Kong (HKU). He graduated with MBChB (Hons) and PhD from the Chinese University of Hong Kong (CUHK) in 1996 and joined HKU as Clinical Assistant Professor in 1999. He obtained his specialist qualification in Haematology and Haematological Oncology in 2003 and was promoted to Clinical Associate Professor and Clinical Professor in 2007 and 2012 respectively.
Dr Edmond Ma obtained MBBS and MD degrees from HKU in 1987 and 2004. He is currently the Director of Clinical and Molecular Pathology at the Hong Kong Sanatorium & Hospital, Honorary Clinical Associate Professor at the Department of Pathology HKU, and Clinical Associate Professor (Honorary) at the Department of Anatomical & Cellular Pathology CUHK. He was previously Vice-President and Chief Examiner in Haematology of the Hong Kong College of Pathologists, and past chairman of the Hong Kong Society for the Study of Thalassaemia and Hong Kong Association of Blood Transfusion & Haematology. He is currently Chairman of the Children's Thalassaemia Foundation.
Dr Edmond Ma obtained MBBS and MD degrees from HKU in 1987 and 2004. He is currently the Director of Clinical and Molecular Pathology at the Hong Kong Sanatorium & Hospital, Honorary Clinical Associate Professor at the Department of Pathology HKU, and Clinical Associate Professor (Honorary) at the Department of Anatomical & Cellular Pathology CUHK. He was previously Vice-President and Chief Examiner in Haematology of the Hong Kong College of Pathologists, and past chairman of the Hong Kong Society for the Study of Thalassaemia and Hong Kong Association of Blood Transfusion & Haematology. He is currently Chairman of the Children's Thalassaemia Foundation.
Descriere
It aims to highlight the pathophysiology, clinical presentations and basic principles in the investigations and managements of haematological diseases prevalent in Asia. Each chapter begins with a real-case clinical scenario, followed by a set of questions and is complemented by photomicrographs, data charts and illustrations.