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Libros sobre el tema "Acute Leukaemia"

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Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 31 de enero de 2023

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1

Olwill, Shane. Annexin II expression in acute myeloid leukaemia. [S.l: The author], 2003.

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2

Barge, A. Acute myeloid leukaemia: The role of haematopoietic growth factors. Macclesfield: Gardner-Caldwell Communications, 1998.

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3

National Institute for Clinical Excellence. Guidance on the use of imatinib for chronic myeloid leukaemia. London: National Institute for Clinical Excellence, 2003.

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4

National Institute for Clinical Excellence. Guidance on the use of imatinib for chronic myeloid leukaemia. London: National Institute for Clinical Excellence, 2002.

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5

Raybould, Simon. Spatial analysis of acute lymphoblastic leukaemia in Tyne and Wear. Newcastle upon Tyne: University of Newcastle upon Tyne Centre for Urban and Regional Development Studies, 1987.

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6

Raybould, Simon. Spatial analysis of acute lymphoblastic leukaemia in Tyne and Wear. Newcastle upon Tyne: University of Newcastle upon Tyne Centre for Urban and Regional Development Studies, 1987.

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7

Coyne, Rose Mary. A study of erythropoietin levels in children with common acute lymphoblastic leukaemia. [s.1: The Author], 1989.

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8

Marwah, Sukhjinder Singh. Role of non-transferrin bound iron in acute leukaemia and sickle cell disease. Wolverhampton: University of Wolverhampton, 2001.

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9

Menasce, Lia Patricia. Deletions of the long arm of chromosome 6 in acute lymphoblastic leukaemia and non-Hodgkin's lymphoma. Manchester: University of Manchester, 1994.

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10

Fitzmaurice, Richard John. Methods for the detection of haemopoietic cells and the assessment of residula haemopoiesis in acute leukaemia. Manchester: University of Manchester, 1993.

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11

1988), Bergamo Spring Conferences on Haematology (2nd. Infections and haemorrhage in acute leukaemia: Proceedings of the conference held in Bergamo on June 13-14, 1988. London: Libbey Eurotext, 1989.

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12

Stankovic, Tatjana. Progress towards the isolation of the gene for ataxia telangiectasia and analysis of clonality in acute leukaemia in children. Birmingham: University of Birmingham, 1995.

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13

Hyde, K. The development of a CFU-GM Bioassay and its relationship to the French American British classification of acute Myeloid Leukaemia. Salford: University of Salford, 1991.

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14

Wood, Alan Christopher. The role of the C-MYC oncogene during drug-induced apoptosis of the acute lymphoblastic leukaemia cell line CCRF C7A. Manchester: University of Manchester, 1994.

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15

Rooney, Maria Anne. An evaluation of the immune competence of children with common Acute Lymphoblastic Leukaemia, both during and post-treatment, by an investigation of the Lymphocyte sub-populations using monoclonal antibodies and the Alkaline Phosphatase Anti-Alkaline Phosphatase technique. [s.1: The Author], 1989.

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16

Collins, Graham y Chris Bunch. Acute leukaemia. Editado por Patrick Davey y David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0286.

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Acute leukaemias are rapidly progressive, clonal haematopoietic stem cell disorders resulting in the accumulation of immature blood cell precursors (known as blasts) in the bone marrow. There are two main types, defined by the presence of myeloid lineage or lymphoid markers on the blast cells: acute myeloid leukaemia and acute lymphoblastic leukaemia. This chapter addresses the causes, diagnosis, and management of the acute leukaemias.
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17

D, Hoelzer y Gökbuget Nicola, eds. Acute lymphocytic leukaemia. London: Baillière Tindall, 2002.

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18

S, Tallman Martin, ed. Acute promyelocytic leukaemia. London: Baillière Tindall, 2003.

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19

K, Burnett Alan, ed. Acute myeloid leukaemia. London: Baillière Tindall, 2001.

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20

D, Hoelzer, ed. Acute lymphoblastic leukaemia. London: Baillière Tindall, 1994.

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21

Acute myeloid leukaemia. London: Baillière Tindall, 2001.

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22

Understanding Acute Myeloblastic Leukaemia. CancerBACUP (British Association of Cancer United, 1990.

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23

CancerBACUP. Understanding Acute Myeloblastic Leukaemia. CancerBACUP (British Association of Cancer United, 1998.

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24

Understanding Acute Lymphoblastic Leukaemia. CancerBACUP (British Association of Cancer United, 1991.

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25

Understanding Acute Lymphoblastic Leukaemia. CancerBACUP (British Association of Cancer United, 2000.

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26

B, Löwenberg, ed. Acute myelogenous leukaemia and myelodysplasia. London: Baillière Tindall, 1996.

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27

Creutzig, Ursula. Acute Myelogenous Leukaemia in Childhood. Springer-Verlag Berlin and Heidelberg GmbH & Co. K, 1990.

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28

Dekker, A. W. Dekker : acute nonlymphocytic leukaemia pb Crs 1: Acute nonlymphocytic leukaemia pb Crs 1. De Gruyter, Inc., 2019.

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29

Provan, Drew, Trevor Baglin, Inderjeet Dokal y Johannes de Vos. Leukaemia. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199683307.003.0004.

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Acute myeloblastic leukaemia (AML) - Acute lymphoblastic leukaemia (ALL) - Chronic myeloid leukaemia (CML) - Chronic lymphocytic leukaemia (B-CLL) - Prolymphocytic leukaemia (PLL) - Hairy cell leukaemia and variant - Large granular lymphocyte leukaemia (LGLL) - Adult T-cell leukaemia-lymphoma (ATLL)
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30

Provan, Drew, Trevor Baglin, Inderjeet Dokal, Johannes de Vos y Hassan Al-Sader. Leukaemia. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199683307.003.0004_update_001.

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Acute myeloblastic leukaemia (AML) - Acute lymphoblastic leukaemia (ALL) - Chronic myeloid leukaemia (CML) - Chronic lymphocytic leukaemia (B-CLL) - Prolymphocytic leukaemia (PLL) - Hairy cell leukaemia and variant - Large granular lymphocyte leukaemia (LGLL) - Adult T-cell leukaemia-lymphoma (ATLL)
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31

Hoelzer, D. Acute Lymphoblastic Leukaemia (Bailliere's Clinical Haematology). Elsevier, 1994.

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32

(Editor), T. Barbui, A. Falanga (Editor), B. Minetti (Editor), S. Gorini (Editor), G. Tognoni (Editor) y M. B. Donati (Editor), eds. Infections and Haemorrhage in Acute Leukaemia. John Libbey & Co Ltd, 1989.

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33

Mendez, Irvin. Acute Myeloid Leukaemia: Symptoms, Diagnosis and Treatment. Nova Science Publishers, Incorporated, 2018.

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34

McCann, Shaun R. Leukaemia. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198717607.003.0007.

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The word leukaemia still is associated with foreboding and a fear of premature death. Steady advances have been made in the treatment of childhood leukaemia but, with notable exceptions, the same is not true in adults. The so-called genetic/molecular revolution has extended the understanding of the pathogenesis of many forms of leukaemia but, as yet, has rarely facilitated cure. With the introduction of tyrosine kinase inhibitor therapy, chronic myeloid leukaemia is the obvious exception but it still needs to be seen as to whether the cytogenetic/molecular revolution can provide cures for many elderly patients with leukaemia, as such patients respond poorly to chemotherapy. Haematopoietic stem cell transplantation, although toxic, expensive, and difficult, still provides a cure for many patients. In spite of all these advances, however, most adults with acute leukaemia or myelodysplastic syndrome are destined to die from their disease, and the causes of these fatal illnesses continue to elude researchers.
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35

Acute leukaemia in childhood with report of a case. [S.l: s.n., 1985.

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36

(Editor), Robert Peter Gale y Dieter Hoelzer (Editor), eds. Acute Lymphoblastic Leukaemia (UCLA symposia on molecular and cellular biology). John Wiley & Sons Inc, 1990.

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37

Gale, Robert Peter. Acute Myelogenous Leukaemia (UCLA Symposia on Molecular and Cellular Biology). John Wiley & Sons Inc, 1990.

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38

Lovat, Penelope Emma. T lymphocyte subpopulations in children receiving chemotherapy for acute lymphoblastic leukaemia. 1991.

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39

M, Carella Angelo, ed. Chronic myeloid leukaemia: Biology and treatment. London: Martin Dunitz, 2001.

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40

Goldman, John M., Angelo M. Carella, George Q. Daley, Connie J. Eaves y Hehlmann Rudiger. Chronic Myeloid Leukaemia: Biology and Treatment. Taylor & Francis Group, 2003.

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41

Carton, James. Haematopathology. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198759584.003.0015.

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This chapter discusses haematopathology, including iron deficiency anaemia, anaemia of chronic disease, megaloblastic anaemias, hereditary spherocytosis, glucose-6-phosphate dehydrogenase deficiency, thalassaemias, sickle-cell disorders, idiopathic thrombocytopenic purpura (ITP), thrombotic thrombocytopenic purpura (TTP), von Willebrand disease, haemophilia, thrombophilia, acute B-lymphoblastic leukaemia, acute myeloid leukaemias, chronic lymphocytic leukaemia (CLL), chronic myelogenous leukaemia, polycythaemia vera (PV), essential thrombocythaemia (ET), primary myelofibrosis (PMF), myelodysplastic syndromes (MDS), follicular lymphoma, diffuse large B-cell lymphoma, Burkitt’s lymphoma (BL), extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma), mantle cell lymphoma, classical Hodgkin’s lymphoma (cHL), lymphoplasmacytic lymphoma (LPL), plasma cell myeloma, primary amyloidosis, and mature T-cell non-Hodgkin’s lymphomas.
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42

Cassidy, Jim, Donald Bissett, Roy A. J. Spence OBE, Miranda Payne y Gareth Morris-Stiff. Bone and soft tissue malignancies. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199689842.003.0025.

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Haematological malignancies examines the epidemiology, genetics, clinical presentation and classification of these diseases, and presents current treatment approaches for each. First are the acute leukaemias, and the management of acute lymphoblastic leukaemia (ALL) and acute myeloid leukaemia (AML). Chronic myeloid leukaemia, its genetics and sensitivity to tyrosine kinase inhibitors, is described. Myelodysplastic syndromes and their management, are followed by chronic lymphoid leukaemias, a large heterogeneous group of diseases, and their treatment. Hodgkin lymphoma, its pathology and presentation, staging and role of PET scanning, is described along with current treatment with chemotherapy and limited radiotherapy. Non-Hodgkin lymphoma is another heterogeneous group of diseases, divided into low-grade and high-grade pathology, and varying in their genetics, presentation, and management. Rituximab is a key component of chemotherapy regimens against B-cell lymphoma. Myeloma and other plasma cell dyscrasias are described, and treatment options reviewed. Myeloma remains incurable, but with appropriate management consistent with prolonged good quality life. Treatment includes chemotherapy, bisphosphonate therapy, analgesics and radiotherapy, Throughout this chapter is emphasised the importance of clinical trials in driving the rapid improvements in treatment of these diseases.
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43

Ajithkumar, Thankamma, Ann Barrett, Helen Hatcher y Natalie Cook. Paediatric malignancies. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199235636.003.0015.

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Leukaemia is the commonest cancer (accounting for >40% of cases) in children. It is a clonal proliferation of stem cells which leads to bone marrow failure and tissue infiltration.• Acute lymphoblastic leukaemia (ALL): 4/100,000• Acute myeloid leukaemia (AML): 0.7/100,000• Chronic myeloid leukaemia (CML): 0.2/100,000...
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44

Glasper, Edward Alan, Gillian McEwing y Jim Richardson, eds. Oncology. Oxford University Press, 2010. http://dx.doi.org/10.1093/med/9780198569572.003.0018.

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Related physiology 596The child with cancer 598Paediatric brain tumours 600Bone tumours 602Neuroblastoma 604Rhabdomyosarcoma (RMS) 606Acute myeloid leukaemia (AML) 608Acute lymphoblastic leukaemia (ALL) 610Wilms tumour 612T-cell acute lymphoblastic leukaemia 614Lymphoma 616Bone-marrow transplantation 618Related skills...
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45

Provan, Drew, Trevor Baglin, Inderjeet Dokal y Johannes de Vos. Paediatric haematology. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199683307.003.0012.

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Blood counts in children - Red cell transfusion and blood component therapy—special considerations in neonates and children - Polycythaemia in newborn and childhood - Neonatal anaemia - Anaemia of prematurity - Haemolytic anaemia in the neonate - Congenital red cell defects - Acquired red cell defects - Haemolytic disease of the newborn - Hyperbilirubinaemia - Neonatal haemostasis - Neonatal alloimmune thrombocytopenia - Congenital dyserythropoietic anaemias - Congenital red cell aplasia - Acquired red cell aplasia - Fanconi anaemia - Rare congenital marrow failure syndromes - Neutropenia in childhood - Disorders of neutrophil function - Childhood immune (idiopathic) thrombocytopenic purpura - Haemolytic uraemic syndrome - Childhood cancer and malignant blood disorders - Childhood lymphoblastic leukaemia - Childhood lymphomas - Childhood acute myeloid leukaemia - Childhood myelodysplastic syndromes and chronic leukaemias - Histiocytic syndromes - Haematological effects of systemic disease in children
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46

Provan, Drew, Trevor Baglin, Inderjeet Dokal, Johannes de Vos y Angela Theodoulou. Paediatric haematology. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199683307.003.0012_update_001.

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Blood counts in children - Red cell transfusion and blood component therapy—special considerations in neonates and children - Polycythaemia in newborn and childhood - Neonatal anaemia - Anaemia of prematurity - Haemolytic anaemia in the neonate - Congenital red cell defects - Acquired red cell defects - Haemolytic disease of the newborn - Hyperbilirubinaemia - Neonatal haemostasis - Neonatal alloimmune thrombocytopenia - Congenital dyserythropoietic anaemias - Congenital red cell aplasia - Acquired red cell aplasia - Fanconi anaemia - Rare congenital marrow failure syndromes - Neutropenia in childhood - Disorders of neutrophil function - Childhood immune (idiopathic) thrombocytopenic purpura - Haemolytic uraemic syndrome - Childhood cancer and malignant blood disorders - Childhood lymphoblastic leukaemia - Childhood lymphomas - Childhood acute myeloid leukaemia - Childhood myelodysplastic syndromes and chronic leukaemias - Histiocytic syndromes - Haematological effects of systemic disease in children
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47

McCann, Shaun R. Molecules, genes, and gene therapy. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198717607.003.0009.

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The twenty-first century has brought many innovations in haematology, with improved diagnostic technology, which may inform treatment choices for malignant diseases, and a better understanding of the genetics and/or epigenetics underlying many diseases. Unfortunately, the aetiology of most of these diseases still eludes us, and some common diseases such as sickle cell disease await simple, inexpensive, and widely available curative treatment. For reasons that are often obscure, some diseases have become fashionable and attract large research financial backing, whereas some do not. With the advent of advanced technology and an improved understanding of disease mechanisms, most haematological malignancies should enjoy the same success as the treatment of childhood acute lymphoblastic leukaemia and chronic myeloid leukaemia.
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48

Acute Leukaemias (Haematology & Blood Transfusion). Springer-Verlag Berlin and Heidelberg GmbH & Co. K, 1994.

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49

Acute Leukaemias (Hamatologie und Bluttransfusion). Springer-Verlag Berlin and Heidelberg GmbH & Co. K, 1992.

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50

McCann, Shaun R. Combination chemotherapy. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198717607.003.0012.

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One of the major advances in haematology during the past six decades has been the development of combination chemotherapy. However, some would dispute the claim that combination chemotherapy has been a major therapeutic advance, arguing that survival for most common cancers has not improved since the advent of chemotherapy. It is certainly true that the survival of children with acute lymphoblastic leukaemia has improved and that the drug imatinib mesylate and its derivatives have changed the outcome for most patients with chronic myeloid leukaemia. Likewise, combination chemotherapy has greatly modified the prognosis for patients with Hodgkin lymphoma and some types of non-Hodgkin lymphoma. However, it must be said that the application of combination chemotherapy to common non-haematological cancers has not met with similar success. In this chapter, the practicalities of the treatment of blood disorders are discussed, with specific reference to the use of this therapy by the medical profession.
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