Haematology : from the image to the diagnosis / Mike Leach, Barbara J. Bain.
By: Leach, Richard M. (Haematologist) [author.]
Contributor(s): Bain, Barbara J [author.]
Language: English Publisher: Hoboken, NJ : Wiley-Blackwell, 2022Description: 1 online resourceContent type: text Media type: computer Carrier type: online resourceISBN: 9781119777502; 9781119777526; 9781119777519Subject(s): Hematologic Diseases -- diagnosis | Blood Physiological PhenomenaGenre/Form: Examination Questions | Electronic books. | Case ReportsDDC classification: 616.1/5 LOC classification: RC636Online resources: Full text is available at Wiley Online Library Click here to view| Item type | Current location | Home library | Call number | Status | Date due | Barcode | Item holds |
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COLLEGE LIBRARY | COLLEGE LIBRARY | 616.15 L468 2022 (Browse shelf) | Available | CL-53014 |
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| 616.132 Se54 2003 An illustrated pocketbook of hypertension / | 616.132061 K1462 2022 Essential manual of 24-hour blood pressure management : from morning to nocturnal hypertension / | 616.15 Ab294 2023 ABC of clinical haematology / | 616.15 L468 2022 Haematology : from the image to the diagnosis / | 616.15 M7321 2020 Molecular hematology / | 616.150758 H6751 2019 Color atlas of clinical hematology : molecular and cellular basis of disease / | 616.2/414 The COVID-19 pandemic : a tribute to the corona whistleblowers / |
ABOUT THE AUTHOR
About the Authors
Mike Leach, MB ChB, FRCP, FRCPath, is Consultant Haematologist and Honorary Senior Lecturer at the Haematology Laboratories and West of Scotland Cancer Centre in Gartnavel General Hospital, Glasgow, UK.
Barbara J. Bain, MB BS, FRACP, FRCPath, is Professor of Diagnostic Haematology at St Mary’s Hospital Campus, Imperial College London, and Consultant Haematologist at St Mary’s Hospital, London, UK.
Includes bibliographical references and index.
TABLE OF CONTENTS
Preface
Abbreviations
1. Haemophagocytic syndrome secondary to anaplastic large cell lymphoma
2. Bone marrow AL amyloidosis
3. Cup-like blast morphology in acute myeloid leukaemia
4. Neutrophil morphology
5. Primary myelofibrosis
6. Sarcoidosis
7. Leishmaniasis
8. Gelatinous transformation of the bone marrow
9. Acanthocytic red cell disorders
10. Large granular lymphocytic leukaemia
11. Pure erythroid leukaemia
12. Reactive mesothelial cells
13. Plasmablastic myeloma
14. Septicaemia
15. Unstable haemoglobin (haemoglobin Köln) and a myeloproliferative neoplasm
16. Sickle cell anaemia in crisis
17. Acute myeloid leukaemia with t(8;21)(q22;q22.1)
18. Chronic neutrophilic leukaemia
19. Essential thrombocythaemia
20. Hairy cell leukaemia
21. Mantle cell lymphoma in leukaemic phase
22. Infantile osteopetrosis
23. Reactive eosinophilia
24. Stomatocytic red cell disorders
25. Reactive lymphocytosis due to viral infection
26. Therapy-related acute myeloid leukaemia with eosinophilia
27. Red cell fragmentation syndromes
28. NK/T-cell lymphoma in leukaemic phase
29. Myelodysplastic syndrome with del(5q)
30. Classical Hodgkin lymphoma
31. Cryoglobulinaemia
32. Congenital dyserythropoietic anaemia
33. Acute monoblastic leukaemia with t(9;11)(p21.3;q23.3)
34. Chronic myeloid leukaemia presenting with myeloid sarcoma and extreme thrombocytosis
35. Glucose-6-phosphate dehydrogenase deficiency
36. Leukaemic presentation of hepatosplenic gamma-delta T-cell lymphoma
37. Myelodysplastic syndromes
38. Pelger–Huët anomaly
39. Russell bodies in lymphoplasmacytic lymphoma
40. T-cell prolymphocytic leukaemia
41. Myeloid maturation arrest
42. MDS/MPN with ring sideroblasts and thrombocytosis
43. Acute myeloid leukaemia with inv(16)(p13.1q22)
44. Babesiosis
45. Haemoglobin E disorders
46. Juvenile myelomonocytic leukaemia
47. Non-haemopoietic tumours
48. Richter transformation of chronic lymphocytic leukaemia
49. Sickle cell-haemoglobin C disease
50. T cell/histiocyte-rich B-cell lymphoma
51. Miliary tuberculosis
52. Pure red cell aplasia
53. Lymphoblastic transformation of follicular lymphoma
54. Primary hyperparathyroidism
55. Gamma heavy chain disease
56. Acute promyelocytic leukaemia with t(15;17)(q24.1;q21.2)
57. AA amyloidosis
58. Acquired sideroblastic anaemia
59. Diffuse large B-cell lymphoma
60. Hickman line infection
61. Monocytes and their precursors
62. Paroxysmal cold haemoglobinuria
63. Transient abnormal myelopoiesis
64. Systemic lupus erythematosus
65. Granular blast cells in acute lymphoblastic leukaemia
66. Chronic myelomonocytic leukaemia
67. Burkitt lymphoma/leukaemia
68. Gaucher’s disease
69. Myelodysplastic syndrome with haemophagocytosis
70. Primary oxalosis
71. Acute myeloid leukaemia with inv(3)(q21.3q26.2)
72. Autoimmune haemolytic anaemia
73. Chronic eosinophilic leukaemia due to FIP1L1-PDGFRA fusion gene
74. Leukaemic phase of follicular lymphoma
75. Megaloblastic anaemia
76. Reactive bone marrow and an abnormal PET scan
77. Acute megakaryoblastic leukaemia
78. Erythrophagocytosis and haemophagocytosis
79. Hyposplenism
80. Acquired haemoglobin H disease
81. Cystinosis
82. Familial platelet disorder with a predisposition to AML
83. Nodular lymphocyte predominant Hodgkin lymphoma
84. Acute monocytic leukaemia with NPM1 mutation
85. Adult T-cell leukaemia/lymphoma
86. Hereditary elliptocytosis and pyropoikilocytosis
87. Sézary syndrome
88. Spherocytic red cell disorders
89. Acute myeloid leukaemia and metastatic carcinoma
90. Chédiak-Higashi syndrome
91. Cortical T-lymphoblastic leukaemia/lymphoma
92. Trypanosomiasis
93. Acute myeloid leukaemia with myelodysplasia-related changes
94. Blastic plasmacytoid dendritic cell neoplasm
95. Inherited macrothrombocytopenias
96. Persistent polyclonal B-cell lymphocytosis
97. Acute myeloid leukaemia with t(6;9)(p23;q34.1)
98. B-cell prolymphocytic leukaemia
99. Various red cell enzyme disorders
100. Sea blue histiocytosis in multiple myeloma
101. Enteropathy-associated T-cell lymphoma
Answers to multiple choice questions and further reflections on the theme
Index
"Despite the tremendous advances that have occurred in diagnostic haematopathology in recent decades haematology remains firmly based on a clinical assessment of the patient, on basic laboratory tests and on a critical assessment of peripheral blood and bone marrow films. In this book we seek to show how an appreciation of blood and bone marrow morphology, assessed with knowledge of the clinical context, can lead to a provisional or, sometimes, a definitive diagnosis that guides further investigation and management. Each of the 101 themes is followed by a related multiple choice question with the preferred answers and further discussion being found in the second part of the book. The themes are sometimes single cases and sometimes a composite of related cases. The book is directed at consultants and trainees in haematology and haematopathology and at clinical and biomedical scientists in these disciplines. We hope that readers will share our enjoyment of the constant sense of discovery that accompanies haematological morphology. All magnifications are stated in terms of the objective used. Common abbreviations that may be used without definition are given on pages xy. Other abbreviations are defined on first use in a theme. All images are of films stained with a May-Grünwald-Giemsa stain unless stated otherwise. The cases are not arranged thematically, since a more random arrangement better approximates to real life. We wish to thank our clinical and laboratory colleagues with whom we have collaborated over many years"-- Provided by publisher.
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