Haematology : from the image to the diagnosis

書誌事項

Haematology : from the image to the diagnosis

Mike Leach, Barbara J. Bain

Wiley-Blackwell, 2022

大学図書館所蔵 件 / 1

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注記

Includes bibliographical references and index

内容説明・目次

内容説明

Haematology Diagnostic haematology requires the assessment of clinical and laboratory data together with a careful morphological assessment of cells in blood, bone marrow and tissue fluids. Subsequent investigations including flow cytometry, immunohistochemistry, cytogenetics and molecular studies are guided by the original morphological findings. These targeted investigations help generate a prompt unifying diagnosis. Haematology: From the Image to the Diagnosis presents a series of cases illustrating how skills in morphology can guide the investigative process. In this book, the authors capture a series of images to illustrate key features to recognize when undertaking a morphological review and show how they can be integrated with supplementary information to reach a final diagnosis. Using a novel format of visual case studies, this text mimics 'real life' for the practising diagnostic haematologist - using brief clinical details and initial microscopic morphological triage to formulate a differential diagnosis and a plan for efficient and economical confirmatory investigation to deduce the correct final diagnosis. The carefully selected, high-quality photomicrographs and the clear, succinct descriptions of key features, investigations and results will help haematologists, clinical scientists, haematology trainees and haematopathologists to make accurate diagnoses in their day-to-day work. Covering a wide range of topics, and including paediatric as well as adult cases, Haematology: From the Image to the Diagnosis is a succinct visual guide which will be welcomed by consultants, trainees and scientists alike.

目次

  • 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 Koeln) 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-Huet 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. Sezary syndrome 88. Spherocytic red cell disorders 89. Acute myeloid leukaemia and metastatic carcinoma 90. Chediak-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

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