Auto-immune disorder, v. Hairy-cell leukaemia. Autoimmune haemolytic anaemia associated

Size: px
Start display at page:

Download "Auto-immune disorder, v. Hairy-cell leukaemia. Autoimmune haemolytic anaemia associated"

Transcription

1 Subject Index Compiled by G. Boehm. Basel = Book Review Acknowledgments 64 Acquired immunodeficiency syndrome, v. AIDS Adult respiratory distress syndrome, v. Blood storage Agglutinins, v. Cold agglutinins Aging, cellular and molecular aspects - The red cell as a model (Progress in clinical and biological research, vol. 195) 62 AIDS (= acquired immune deficiency syndrome); first case in Italy of fatal AIDS in a haemophilic ; persistent cold agglutinins in AIDS and related disorders 171 Alder anomaly accompanied by a mutation of the myeloperoxidase structural gene 157 Algeria; changes in patterns of leukaemia in Algeria, Anaemia; dyserythropoietic, congenital, -----; glycosylated haemoglobin levels in a benign form of sickle cell anaemia in Saudi Arabia ; haemolytic; primary malignant lymphoma of the uterine cervix associated with cold-reacting auto-antibody-mediated haemolytic anaemia ; haemolytic, autoimmune, associated -----; sickle-cell anaemia, lymphocyte subpopulations 60 Anaemias haemolytic, vol. I (The hereditary haemolytic anaemias, part I, 3rd ed.) ; immune hemolytic anaemias (Methods in hematology, vol. 12) 62 Antibodies, v. Antineutrophil antibodies Antibodies, monoclonal, v. Bernard-Soulier; Leukaemia, lymphocytic, chronic (OKT4+); Platelets, human Antibody to neutrophils associated with autoimmune neutropenia, analysis: possible recognition of Fc-receptor-related molecules 236 Anticoagulant, v. Lupus-type anticoagulant Antineutrophil antibodies in neutropenic patients, diagnostic usefulness of measuring 65 Antioxidative systems; effects of blood storage on red ceil antioxidative systems 30 Antiplatelet antibodies, v. Platelets, human Antithrombin III during high-dose cytosin arabinoside therapy with or without asparaginase 96 Aortic occlusion; acute myelocytic leukaemia with acute aortic occlusion as presenting symptom 120 Asparaginase; antithrombin III during high-dose cytosin arabinoside therapy with or without asparaginase 96 Autoantibodies, v. Cold-reacting autoantibodies Auto-immune disorder, v. Hairy-cell leukaemia Autoimmune haemolytic anaemia associated Autoimmune neutropenia, v. Neutrophils, antibody Automated cytochemistry, v. Cytochemistry B cell chronic lymphocytic leukaemia and lung carcinoma with T-lymphocyte-rich pleural effusion in a single patient 110 Bence Jones protein, v. Monoclonal immunoglobulins Bernard-Soulier syndrome: diagnosis by an ELISA method using monoclonal antibodies in 2 new unrelated patients 203 B-immunoblastic lymphoma arising in angioimmunoblastic lymphadenopathy 105 Biopsy pathology of bone and bone marrow (Biopsy pathology series) 62 Blood coagulation, v. Coagulation of blood Blood diseases 61 Blood elements; radiolabeled cellular blood elements (Pathophysiology, techniques and scintigraphic applications) 127 Blood storage, effects on red cell antioxidative systems 30 Blood transfusion; plasma fractionation and blood transfusion (Developments in hematology and immunology) ; v. Therapy, supportive..., Transfusion Bone and bone marrow, biopsy pathology (Biopsy pathology series) 62 Bone marrow fibroblasts; increased collagen synthesis of bone marrow fibroblasts by materials released from platelets of chronic granulocytic leukaemia and polycythaemia Bone marrow transplant; unexpected presentation of deep candidiasis in a recipient of a mismatched bone marrow transplant 116 Book reviews 61-63, , 192 Calcium dobesilate, v. Platelet-activating factor ( PA F) Candidiasis; unexpected presentation of deep candidiasis in a recipient of a mismatched bone marrow transplant 116 Carcinoma, v. Lung carcinoma Cell kinetics; analysis of human myeloma cell population kinetics 153 Cell surface molecules on human platelets, analysis with monoclonal antibodies (I. Identification of four platelet-specific surface molecules) ; (II. Diversity of antibodybinding sites Chemotherapy, v. Lithium Childhood idiopathic myelofibrosis, highdose intravenous corticosteroid treatment Chromosomes; a new chromosome translocation (3; 21) in M2 acute lymphocytic leukaemia ; variant translocation t (7; 9; 22) during lymphoid blastic crisis in a case of Ph'-positivechronicmyelogenous leukaemia with previous Epstein-Barr virus infection 46 Coagulation of blood, v. Anticoagulant (lupus type), Antithrombin III, Bernard-Soulier syndrome, Factor X, Haemorrhage, Plasminogen, Platelet(s), Thrombocytopenia, Thrombocytopenic purpura, Thrombocytosis, Thrombotic tendency Cold agglutinins, persistent, in AIDS and related disorders 171 Cold-insoluble globulin, v. Fibronectin Cold-reacting autoantibodies; primary malignant lymphoma of the uterine cer

2 Subject Index 247 vix associated with cold-reacting antibody-mediated haemolytic anaemia 232 Collagen synthesis; increased collagen synthesis of bone marrow fibroblasts by materials released from platelets of chronic granulocytic leukaemia and polycythaemia Congenital dyserythropoietic anaemia Congenital heterozygous plasminogen deficiency associated with a severe thrombotic tendency 54 Corticosteroid treatment with high intravenous dose in childhood idiopathic myelofibrosis Cytarabine, low dose in myelodysplastic syndromes and acute leukaemia (A comment) ; reply 126 Cytochemistry, automated, in non-hodgkin s lymphoma: a new method for determination of cells from lymph node biopsy 199 Cytoplasmic immunoglobulins; phenotypic characterization of adult acute lymphoblastic leukaemia: are cytoplasmic immunoglobulins related to prognosis? 190 Cytosin arabinoside therapy; anti-thrombin III during high-dose cytosine arabinoside therapy with or without asparaginase 96 Deoxinucleotidyl transferase (TdT); incidence of TdT positivity in cases of leukaemia and lymphoma 12 Diabetic microangiopathy, v. Platelet-activating factor (PAF) Diagnosis, v. Bernard-Soulier syndrome Diagnostic usefulness of measuring antineutrophil antibodies in neutropenic patients 65 Dyserythropoietic anaemia, congenital, Electron microscope (transmission), Dyserythropoietic anaemia, v. Mastocytoma, Toxic oil syndrome ELISA (= enzyme-linked immuno sorbent assay) method; Bernard-Soulier syndrome: diagnosis by an ELISA method using monoclonal antibodies in 2 new unrelated patients 203 Elliptocytosis and schistocytosis in myelodysplasia; Report of two cases 174 Energetic state (red blood cells) v. Redox... Enzymatic analysis, methods, vol. 7,3rd ed. metabolites 2: Tri-and dicarboxylix acids, purines, pyrimidines and derivatives, coenzymes, inorganic compounds ; vol. 8, 3rd ed. metabolites 3: Lipids, amino acids and related compounds 61 Eosinophils (ultrastructure), v. Toxic oil syndrome Epstein-Barr virus; variant translocation t (7; 9; 22) during lymphoid blastic crisis in a case of Ph'-positive chronic myelogenous leukaemia with previous Epstein- Barr virus infection 46 Erythrocytes; cellular and molecular aspects of aging - The red cell as a model (Progress in clinical and biological research, vol. 195) ; effects of blood storage on red cell antioxidative systems ; hereditary leaky red cell syndrome in a Swiss family ; redox and energetic state of red blood cells in G6PD deficiency, heterozygous /3-thalassaemia and the combination of both 211 Erythrophagocytosis, v. Phagocytic plasma cells Estrogen and progesteron receptor guideline for tamoxifen therapy in chronic lymphocytic leukaemia: a pilot study 92 Evan's syndrome, chronic active hepatitis and focal glomerulonephritis in IgA deficiency 1 Factor X (= Stuart-Prower factor) variants, tentative and updated classifications 58 Families, v. Bernard-Soulier syndrome, Dyserythropoietic anaemia, Hereditary leaky red cell..., Plasminogen Fc receptor, v. Neutrophils, antibody Ferments, v. Antioxidative systems (erythrocytes), Asparaginase, Deoxinucleotidyl transferase, Enzymes, Glucose- 6-phosphate dehydrogenase, Myeloperoxidase Fibroblasts, v. Bone marrow fibroblasts Fibronectin; plasma fibronectin in sickle cell disease ; plasma fibronectin structure and function (Hematology, vol. 3) 192 Flow cytochemistry, automated, v. Cytochemistry, automated Gammopathy, biclonal, v. Myeloma, multiple Gammopathy, monoclonal; phagocytic plasma cells and Russell bodies in monoclonal gammopathy of undetermined -----; v. Monoclonal immunoglobulins Gc protein (vitamin D binding protein) on the surface of normal human lymphocytes and leukaemic lymphocytes, distribution 26 Genetic changes, v. Myeloperoxidase Genetic rearrangements in leukaemia and lymphoma (Leukaemia and lymphoma research, vol. 2) 128 Glomerulonephritis; Evan s syndrome, chronic active hepatitis and focal glomerulonephritis in IgA deficiency 1 Glucose-6-phosphate dehydrogenase (G6PD) deficiency; redox and energetic state of red blood cells in G6PD deficiency, heterozygous /Fthalassaemia and the Glycosylated haemoglobin levels in a benign form of sickle cell anaemia in Saudi Arabia 160 Haematological neoplasias, v. Cytosin arabinoside therapy Haematology, manual 128 Haematology, methods, vol. 12; immune haemolytic anaemias 62 Haematology; radionuclides in haematology 192 Haematology, recent advances, vol Haematology, supportive therapy 62 Haemoglobin; experimental approaches for the study of haemoglobin switching (Progress in clinical and biological research, vol. 191) ; glycosylated haemoglobin levels in a benign form of sickle cell anaemia in Saudi Arabia 160 Haemoglobinuria, paroxysmal, nocturnal; autoimmune haemolytic anaemia associated Haemolytic anaemias, vol. I (The hereditary haemolytic anaemias, part I, 3rd ed.)61 Haemolytic anaemias; immune hemolytic anemias (Methods in hematology, vol. 12) 62 Haemolytic disorder, v. Hereditary leaky red cell... Haemophilia A; first case in Italy of fatal AIDS in haemophilia 34 Haemopoietic progenitor cells, committed and pluripotent, circulating in infants 18 Haemorrhage, intracerebral, by acute myelofibrosis 38

3 248 Subject Index Haemorrhage, subdural, in a 32-year-old Hairy-cell leukaemia associated with autoimmune disorders in the form of a lupustype anti-coagulant and a positive direct Coombs test 181 Hemalog D, v. Cytochemistry, automated Hemolytic anemias; immune hemolytic anemias (Methods in hematology, vol. 12) 62 Hematology, methods, vol. 12; immune hemolytic anemias 62 Hepatitis; Evan s syndrome, chronic active hepatitis and focal glomerulonephritis in IgA deficiency I Hereditary leaky red cell syndrome in a Swiss family 70 Hodgkin, v. Non-Hodgkin s... HTLV-III virus ( - Human T-cell lymphotropic virus-type III), v. AIDS Human leukemia, modern trends VI (New results in clinical and biological research including pediatric oncology, haematology and blood transfusion) 128 Human platelets, v. Platelets, human Idiopathic thrombocytopenic purpura; T- lymphocyte subsets and platelet-associated purpura: effect of splenectomy ; subdural haemorrhage in a 32-yearold IgA deficiency; Evan s syndrome, chronic active hepatitis and focal glomerulonephritis in IgA deficiency 1 IgG, v. Idiopathic thrombocytopenic purpura Immune hemolytic anemias (Methods in hematology, vol. 12) 62 Immunoblastic lymphoma, v. Lymphoma Immunoglobulins, monoclonal, v. Non- Hodgkin s lymphoma Infants, v. Childhood, Haemopoietic progenitor cells Iron-binding total capacity, effects of transferrin genetic phenotypes 215 Italy, v. AIDS Leukaemia, acute; low-dose cytarabine in myelodysplastic syndromes and acute leukaemia (A comment) ; reply ; a case of leukaemic mastocytoma terminating in metamorphosis ; B-cell lymphocytic, chronic, and lung carcinoma with T-lymphocyte-rich pleural effusion in a single patient ; granulocytic, chronic; increased collagen synthesis of bone marrow fibroblasts by materials released from platelets of chronic granulocytic leukaemia and polycythaemia -----; hairy-cell leukaemia, associated with auto-immune disorders in the form of a lupus-type anti-coagulant and positive direct Coombs test ; human, modern trends IV (New results in clinical and biological research, including pediatric oncology, haematology and blood transfusion) ; incidence of deoxynucléotidyl transferase positivity in leukaemia and lymphoma 12 Leukaemia, lymphatic, v. Leukaemia, T- cell lymphatic ; lymphoblastic, acute, adult, phenotypic characterization: are cytoplasmic immunoglobulins related to prognosis? ; lymphoblastic, T-acute, in adults, related to transitional cortical-medullary thymocytes with surface markers of the CD4 subset ; lymphocytic, v. Lymphocytes, human... Leukaemia, lymphocytic, chronic; estrogen and progesteron receptor guideline for tamoxifen therapy in chronic lymphocytic leukaemia: a pilot study ; OKT4+ chronic lymphocytic leukaemia cells display different reactivity with selected monoclonal antibody combinations ; with leukaemic meningitis ; untreated, v. Leukaemia, myeloid, acute Leukaemia and lymphoma, genetic rearrangements (Leukaemia and lymphoma research, vol. 2) 128 Leukaemia, myelocytic, acute, with acute aortic occlusion as presenting symptom ; myelogenous, acute, correlative patterns of leukocyte counts at presentation and relapse ; myeloid, acute, developing in a patient with longstanding untreated chronic lymphocytic leukaemia ; non-lymphocytic, acute (M2); a new chromosome translocation (3:21) in M2 acute lymphocytic leukaemia ; T-cell lymphatic, chronic; T activation in a patient with T cell chronic lymphatic leukaemia 122 Leukaemias; changes of patterns in leukaemia in Algeria, ; therapy, v. Cytosine arabinoside therapy Leukaemic mastocytoma, a case, terminating in metamorphosis 40 Leukaemic meningitis in chronic lymphocytic leukaemia 113 Leukocyte counts; correlative patterns of leukocyte counts at presentation and relapse in acute myelogenous leukaemia 79 Leukocyte function, regulation (Contemporary topics in immunobiology, vol. 14) 128 Leukocytes, granules, v. Alder anomaly Lithium, effects on the platelet count in neoplastic patients treated with polychemotherapy 242 Lung carcinoma; B cell chronic lymphocytic leukaemia and lung carcinoma with T- lymphocyte-rich pleural effusion in a single patient 110 Lupus-type anticoagulant; hairy-cell leukaemia associated with auto-immune disorders in the form of a lupus-type anticoagulant and a positive direct Coombs test 181 Lymph node biopsy; automated cytochemistry in non-hodgkin s lymphoma: a new method for determination of cells from lymph node biopsy 199 Lymphadenopathy; B-immunoblastic lymphoma arising in angioimmunoblastic lymphadenopathy 105 Lymphocyte subpopulations in sickle-cell anaemia 60 Lymphocytes, human, normal and leukaemic; distribution of Gc protein; (vitamin D binding protein) on the surface of normal and leukaemic lymphocytes 26 Lymphocytes, v. Leukaemia, lymphocytic, chronic (OK.T4*); Thymocytes Lymphoma and leukaemia, genetic rearrangements (Leukaemia and lymphoma research, vol. 2) 128 Lymphoma; B-immunoblastic lymphoma arising in angioimmunoblastic lymphadenopathy ; incidence of deoxynucléotidyl transferase positivity in cases of leukaemia and lymphoma ; primary malignant of the uterine cervix associated with cold-reacting autoantibody-mediated haemolytic anaemia ; v. Non-Hodgkin s lymphoma Manual of haematology 128 Mastocytoma; a case of leukaemic mastocytoma terminating in metamorphosis 40

4 Subject Index 2 Membranes of erythrocytes, v. Hereditary leaky red cell... Meningitis, v. Leukaemic meningitis Methods of enzymatic analysis, vol. 7, 3rd ed. metabolites 2: Tri- and dicarboxylic acids, purines, pyrimidines and derivatives, coenzymes, inorganic compounds ; vol. 8, 3rd ed. metabolites: 3: Lipids, amino acids and related compounds 61 Methods in hematology, vol. 12; immune hemolytic anaemias 62 Methods, v. Cytochemistry, automated; ELISA method Microangiopathy; platelet-activating factor (PAF) - A powerful lipid autacoid possibly involved in microangiopathy (A review) 129 Monoclonal antibodies; analysis of cell surface molecules on human platelets with monoclonal antibodies (I. Identification of four platelet-specific surface molecules) ; (Diversity of antibody-binding sites Monoclonal antibodies, v. Bernard-Soulier syndrome; Leukaemia, lymphocytic, chronic (OKT4*); Platelets, human Monoclonal immunoglobulins; serum and urine monoclonal immunoglobulins in malignant non-hodgkin s lymphoma 193 Multiple myeloma, v. Myeloma Myelodysplasia; elliptocytosis and schistocytosis in myelodysplasia: Report of two cases 174 Myelodysplastic syndromes; low-dose cytarabine in myelodysplastic syndromes and acute leukaemia (A comment) reply 126 Myelofibrosis, acute, with associated intracerebral haemorrhage ; high-dose intravenous corticosteroid treatment in childhood idiopathic myelofibrosis Myeloma, human, cell population kinetics, analysis 153 Myeloma, multiple and coincident non- Hodgkin s lymphoma with 2 serum monoclonal immunoglobulins ; v. Paraproteinaemia, double Myeloperoxidase; Alder anomaly accompanied by a mutation of the myeloperoxidase structural gene 157 Neoplastic patients, treated with polychemotherapy, effects of lithium on the platelet count 242 Neutropenia, autoimmune, v. Neutrophils, antibody Neutropenic patients; the diagnostic usefulness of measuring antineutrophil antibodies in neutropenic patients 65 Neutrophils, antibody; analysis of antibody to neutrophils associated with autoimmune neutropenia: possible recognition of Fc-receptor-related molecules 236 Neutrophils, v. Alder anomaly Non-Hodgkin s lymphoma; automated cytochemistry in non-hodgkin s lymphoma: a new method for determination of cells from lymph node biopsy ; serum and urine monoclonal immunoglobulins in malignant non-hodgkin s lymphoma ; and coincident multiple myeloma with 2 serum monoclonal immunoglobulins ; new techniques and treatments 127 Oxidation, v. Antioxidative systems PAF (= Platelet-activating factor). A powerful lipid autacoid possibly involved in microangiography (A review) 129 Paraproteinaemia, double (IgAK+ IgGK)in a single patient: immunofluorescence evidence for a common plasma cell clone frozen at the switch phase 224 Paroxysmal nocturnal haemoglobinuria, v. Haemoglobinuria Phagocytic plasma cells and Russell bodies in monoclonal gammopathy of undetermined Plasma cell clone, v. Paraproteinaemia, double Plasma cell myeloma, v. Myeloma, human Plasma cells, phagocytic, and Russell bodies in monoclonal gammopathy of undetermined Plasma fractionation and blood transfusion (Developments in hematology and immunology) 63 Plasma fibronectin in sickle cell disease 209 Plasma fibronectin, structure and function (Hematology, vol. 3) 192 Plasminogen, congenital, heterozygous, deficiency, associated with severe thrombotic tendency 54 Platelet activating factor (PAF); a powerful lipid autacoid possibly involved in microangiography (A review) 129 Platelet count in neoplastic patients treated with polychemotherapy, effects of lithium 242 Platelet membrane glycoproteins, v. Bernard-Soulier syndrome Platelets, human; analysis of cell surface molecules on human platelets with monoclonal antibodies (1. Identification of four platelet-specific molecules) ; (II. Diversity of antibodybinding sites -----; increased collagen synthesis of bone marrow fibroblasts by materials released from platelets of chronic granulocytic leukaemia and polycythaemia -----; v. Purpura, thrombocytopenic... Pleural effusion; B cell chronic lymphocytic leukaemia and lung carcinoma with T-lymphocyte-rich pleural effusion in a single patient 110 Polycythaemia vera; increased collagen synthesis of bone marrow fibroblasts by material released from platelets of chronic granulocytic leukaemia and polycythaemia Progenitor cells, circulating, v. Haemopoietic progenitor cells Progesteron receptor, v. Estrogen Prognosis (lymphoblastic leukaemia), v. Cytoplasmic immunoglobulins Purpura, thrombocytopenic, idiopathic; subdural haemorrhage in a 32-year-old -----; T-lymphocyte subsets and plateletassociated purpura: effect of splenectomy 83 Radiolabeled cellular blood elements (Pathophysiology, techniques, and scintigraphic applications) 127 Radionuclides in haematology 192 Rapeseed oil, denaturated; toxic oil syndrome, ultrastructural study of blood cells 165 Red blood cells; redox and energetic state of red blood cells in G6PD deficiency, heterozygous /3-thalassaemia and the Red cell antioxidative systems, effects of blood storage 30 Red cells, leaky; hereditary leaky red cell syndrome in a Swiss family 70 Red cells, v. Aging Redox and energetic state of red blood cells in G6PD deficiency, heterozygous /)-thalassacmia and the combination of both 211

5 250 Subject Index Rheumatoid arthritis; autoimmune haemolytic anaemia associated with rheumatoid arthritis and paroxysmal nocturnal haemoglobinuria 241 Russell bodies; phagocytic plasma cells and Russell bodies in monoclonal gammopathy of undetermined Saudi Arabia; glycosylated haemoglobin levels in a benign form of sickle cell anaemia in Saudi Arabia ; studies on sickle cell heterozygotes in Saudi Arabia - Interaction with a-thalassaemia 100 Schistocytosis and elliptocytosis in myelodysplasia: Report of two cases 174 Serum monoclonal immunoglobulins, v. Monoclonal immunoglobulins Siblings, v. Dyserythropoietic anaemia, congenital Sickle cell anaemia; glycosylated haemoglobin levels in a benign form of sickle cell anaemia ; lymphocyte subpopulations 60 Sickle cell disease ; plasma fibronectin 209 Sickle cell heterozygotes in Saudi Arabia, studies - Interaction with «-thalassaemia 100 Soulier..., v. Bernard... Splenectomy; T-Iymphocyte subsets and platelet-associated IgG in idiopathic thrombocytopenic purpura: effect of splenectomy 83 Subdural haemorrhage, v. Haemorrhage Swiss family; hereditary leaky red cell syndrome in a Swiss family 70 Switching myeloma cell clone; double (IgAk + IgGk) paraproteinaemia in a single patient: immunofluorescence evidence for a common plasma cell clone frozen at the switch phase 224 T activation in a patient with T cell chronic lymphatic leukaemia 122 T-acute lymphoblastic leukaemia, v. Leukaemia, lymphoblastic, T-acute Tamoxifen therapy; estrogen and progesterone receptor guideline for tamoxifen therapy in chronic lymphocytic leukaemia: a pilot study 92 Thalassaemia (alpha); studies on sickle cell heterozygotes in Saudi Arabia - Interaction with a-thalassaemia 100 Thalassaemia (beta); redox and energetic state of red blood cells in G6PD deficiency, heterozygous /(-thalassaemia and the Therapy, supportive, in haematology 62 Therapy, v. Cytosin-arabinoside therapy, Tamoxifen Thrombocytopenia, v. Bernard-Soulier syndroma Thrombocytopenic, idiopathic, purpura; subdural haemorrhage in a 32-year-old -----; T-lymphocyte subsets and platelet associated purpura: effect of splenectomy 83 Thrombocytosis; acquired type I von Willebrand s disease in a patient with essential thrombocytosis 188 Thrombotic tendency; congenital heterozygous plasminogen deficiency associated with severe thrombotic tendency 54 Thymocytes; adult T-acute lymphoblastic leukaemia related to transitional corticalmedullary thymocytes with surface markers of the CD4 subset 52 T-lymphocyte subsets and platelet-associated purpura: effect of splenectomy 83 T-lymphocytic leukaemia, v. Leukaemia, lymphocytic, chronic (OKT4+) Toxic oil (denaturated rapeseed oil) syndrome, ultrastructural study of blood cells 165 Transferase, v. Deoxinucleotidyl transferase Transferrin genetic phenotypes, effects on total iron-binding capacity 215 Transfusion; plasma fractionation and blood transfusion (Development in hematology and immunology) ; v. Blood storage; Therapy, supportive... Transplantation, v. Bone marrow transplant (candidiasis) Ultrastructural study of blood cells in toxic oil syndrome 165 Ultrastructure, v. Dyserythropoietic anaemia, Mastocytoma Urine imunoglobulins, v. Monoclonal immunoglobulins Uterine cervix, v. Lymphoma, primary malignant Viral infection, v. AIDS Vitamin D binding protein Gc: distribution on the surface of normal human lymphocytes and leukaemic lymphocytes 26 Von Willebrand s disease, acquired, type I, in a patient with essential thrombocytosis 188 Willebrand, v. Von Willebrand

Contents SECTION 1: PHYSIOLOGY OF BLOOD

Contents SECTION 1: PHYSIOLOGY OF BLOOD Contents SECTION 1: PHYSIOLOGY OF BLOOD Chapter 1: Overview of Physiology of Blood 1 Normal Haematopoiesis 1 Red Blood Cells 6 White Blood Cells 15 Immune System 27 Megakaryopoiesis 32 Normal Haemostasis

More information

Anticoagulant circulating, in systemic lupus erythematosus: clinical manifestations. Anticoagulant clinics, frequency of attendance

Anticoagulant circulating, in systemic lupus erythematosus: clinical manifestations. Anticoagulant clinics, frequency of attendance Subject Index Compiled by G.Boehm, Basel = Book Review Advances, recent, in blood coagulation, vol.4 182 Ah locus; acute haematoxicity of oral benzo(a)pyrene: the role the Ah locus Agglutinins; cold agglutinins

More information

r). SUPPLEMENTARY/SECOND OPPORTUNITY EXAMINATION PAPER nnmlbih UNIVERSITY Sophia Blaauw INSTRUCTIONS FACULTY OF HEALTH AND APPLIED SCIENCES

r). SUPPLEMENTARY/SECOND OPPORTUNITY EXAMINATION PAPER nnmlbih UNIVERSITY Sophia Blaauw INSTRUCTIONS FACULTY OF HEALTH AND APPLIED SCIENCES r). nnmlbih UNIVERSITY OF SCIEFICE nnd TECHNOLOGY FACULTY OF HEALTH AND APPLIED SCIENCES DEPARTMENT OF HEALTH SCIENCES QUALIFICATION: BACHELOR OF MEDICAL LABORATORY SCIENCES QUALIFICATION CODE: 08BMLS

More information

12 Dynamic Interactions between Hematopoietic Stem and Progenitor Cells and the Bone Marrow: Current Biology of Stem Cell Homing and Mobilization

12 Dynamic Interactions between Hematopoietic Stem and Progenitor Cells and the Bone Marrow: Current Biology of Stem Cell Homing and Mobilization Table of Contents: PART I: Molecular and Cellular Basis of Hematology 1 Anatomy and Pathophysiology of the Gene 2 Genomic Approaches to Hematology 3 Regulation of Gene Expression, Transcription, Splicing,

More information

Angiotensin; serum angiotensin-iconverting

Angiotensin; serum angiotensin-iconverting Subject Index Compiled G. Boehm, Basel (B) = Book Reviews Acetaldehyde influences glucose 1,6-biphosphate level of human erythrocytes in vitro and in vivo 241 Adenocarcinoma of the colon; acquired factor

More information

The primary medical content categories of the blueprint are shown below, with the percentage assigned to each for a typical exam:

The primary medical content categories of the blueprint are shown below, with the percentage assigned to each for a typical exam: Hematology Certification Examination Blueprint Purpose of the exam The exam is designed to evaluate the knowledge, diagnostic reasoning, and clinical judgment skills expected of the certified hematologist

More information

SYLLABUS ON HEMATOLOGY FOR THE 4-YEAR STUDENTS, MEDICINE-2. Total hours number 70 hours, including course 20 hours, seminars 50 hours.

SYLLABUS ON HEMATOLOGY FOR THE 4-YEAR STUDENTS, MEDICINE-2. Total hours number 70 hours, including course 20 hours, seminars 50 hours. SYLLABUS ON HEMATOLOGY FOR THE 4-YEAR STUDENTS, MEDICINE- Total hours number 70 hours, including course 0 hours, seminars 0 hours. Aim of the subject of Hematology: The study of etiology, pathogenesis,

More information

HAEMATOLOGICAL MALIGNANCY

HAEMATOLOGICAL MALIGNANCY HAEMATOLOGICAL MALIGNANCY Reference Compulsory reading Haematology at Glance 2 nd ed. Atul Mehta & Victor Hoffbrand Chapters: 20 to 31 Pages: 46 to 69 Pathogenesis of Haematological Malignancy Figure (a)

More information

The Power of Peripheral Blood Smears: Apparent Diagnostic Clues (Part 1) (Wednesday, October 19, 2011)

The Power of Peripheral Blood Smears: Apparent Diagnostic Clues (Part 1) (Wednesday, October 19, 2011) The Power of Peripheral Blood Smears: Apparent Diagnostic Clues (Part 1) (Wednesday, October 19, 2011) By Gene Gulati, Ph.D., SH(ASCP) Conflict of Interest None Plan for the Course Review blood smears,

More information

Index. Note: Page numbers of article titles are in boldface type.

Index. Note: Page numbers of article titles are in boldface type. Note: Page numbers of article titles are in boldface type. A Acute lymphoblastic leukemia, in India, 439 440 pediatric, global approach to, 420 424 core resources in low- and middle-income countries, 423

More information

HEMATOLOGY Maintenance of Certification (MOC) Examination Blueprint

HEMATOLOGY Maintenance of Certification (MOC) Examination Blueprint HEMATOLOGY Maintenance of Certification (MOC) Examination Blueprint ABIM invites diplomates to help develop the Hematology MOC exam blueprint Based on feedback from physicians that MOC assessments should

More information

Form 2033 R3.0: Wiskott-Aldrich Syndrome Pre-HSCT Data

Form 2033 R3.0: Wiskott-Aldrich Syndrome Pre-HSCT Data Key Fields Sequence Number: Date Received: - - CIBMTR Center Number: CIBMTR Recipient ID: Has this patient's data been previously reported to USIDNET? USIDNET ID: Today's Date: - - Date of HSCT for which

More information

There are two main causes of a low platelet count

There are two main causes of a low platelet count Thrombocytopenia Thrombocytopenia is a condition in which a person's blood has an unusually low level of platelets Platelets, also called thrombocytes, are found in a person's blood along with red blood

More information

Myeloproliferative Disorders - D Savage - 9 Jan 2002

Myeloproliferative Disorders - D Savage - 9 Jan 2002 Disease Usual phenotype acute leukemia precursor chronic leukemia low grade lymphoma myeloma differentiated Total WBC > 60 leukemoid reaction acute leukemia Blast Pro Myel Meta Band Seg Lymph 0 0 0 2

More information

QUESTIONS OF HEMATOLOGY AND THEIR ANSWERS

QUESTIONS OF HEMATOLOGY AND THEIR ANSWERS QUESTIONS OF HEMATOLOGY AND THEIR ANSWERS WHAT IS TRUE AND WHAT IS FALSE? Questions 1 Iron deficiency anemia a) Is usually associated with a raised MCV. b) The MCH is usually low. c) Is most commonly due

More information

YEREVAN STATE MEDICAL UNIVERSITY DEPARTMENT OF HEMATOLOGY COURSE DESCRIPTION HEMATOLOGY

YEREVAN STATE MEDICAL UNIVERSITY DEPARTMENT OF HEMATOLOGY COURSE DESCRIPTION HEMATOLOGY 1. Module/unit Code II. 1.2. 2. Module/unit Title Hematology 3. Subject Field Internal Diseases Group 4. Faculty/Department General Medicine, Department of Hematology 5. Programme(s) to which the Doctor

More information

Dairion Gatot, Soegiarto Ganie, Savita Handayani. Divisi Hematologi & Onkologi Medik Departemen Ilmu Penyakit Dalam FK-USU/RS H.Adam Malik Medan 2009

Dairion Gatot, Soegiarto Ganie, Savita Handayani. Divisi Hematologi & Onkologi Medik Departemen Ilmu Penyakit Dalam FK-USU/RS H.Adam Malik Medan 2009 HAEMOLYTIC ANAEMIA Dairion Gatot, Soegiarto Ganie, Savita Handayani. Divisi Hematologi & Onkologi Medik Departemen Ilmu Penyakit Dalam FK-USU/RS H.Adam Malik Medan 2009 WHEN BY THEN Hb 9 g% transfusion

More information

July 3, The Physician Compare Team Centers for Medicare and Medicaid Services 7500 Security Boulevard Baltimore, MD 21244

July 3, The Physician Compare Team Centers for Medicare and Medicaid Services 7500 Security Boulevard Baltimore, MD 21244 July 3, 2013 The Physician Compare Team Centers for Medicare and Medicaid Services 7500 Security Boulevard Baltimore, MD 21244 Re: Physician Compare Intelligent Search To Whom it May Concern, The American

More information

Hematology Page 1 of 8

Hematology Page 1 of 8 Hematology Page 1 of 8 Hematology Major Category Code Headings Revised 12/17 1 Basic methodology and test armamentarium 20000 2 Normal hematopoiesis & hemostasis 20100 3 RBC disorders, non-neoplastic 20340

More information

Hematology Unit Lab 2 Review Material

Hematology Unit Lab 2 Review Material Objectives Hematology Unit Lab 2 Review Material - 2018 Laboratory Instructors: 1. Assist students during lab session Students: 1. Review the introductory material 2. Study the case histories provided

More information

Angioimmunoblastic lymphadenopathy, v. Lymphadenopathy Anisocytosis, v. Lymphocyte anisocytosis

Angioimmunoblastic lymphadenopathy, v. Lymphadenopathy Anisocytosis, v. Lymphocyte anisocytosis Subject Index Compiled G. Boehm. Basel (B = Book Review) Acquired immunodeficiency syndrome (AIDS), erythroblastopenia 273 Adults, young, myelofibrosis 396 Advances, recent, in haematology, vol.3(1982)

More information

Index. Note: Page numbers of article titles are in boldface type.

Index. Note: Page numbers of article titles are in boldface type. Note: Page numbers of article titles are in boldface type. A Abdominal tumors, in children, 530 531 Alkalinization, in tumor lysis syndrome, 516 Allopurinol, in tumor lysis syndrome, 515 Anaphylaxis, drug

More information

HEMATOLOGIC MALIGNANCIES BIOLOGY

HEMATOLOGIC MALIGNANCIES BIOLOGY HEMATOLOGIC MALIGNANCIES BIOLOGY Failure of terminal differentiation Failure of differentiated cells to undergo apoptosis Failure to control growth Neoplastic stem cell FAILURE OF TERMINAL DIFFERENTIATION

More information

CHAPTER:4 LEUKEMIA. BY Mrs. K.SHAILAJA., M. PHARM., LECTURER DEPT OF PHARMACY PRACTICE, SRM COLLEGE OF PHARMACY 8/12/2009

CHAPTER:4 LEUKEMIA. BY Mrs. K.SHAILAJA., M. PHARM., LECTURER DEPT OF PHARMACY PRACTICE, SRM COLLEGE OF PHARMACY 8/12/2009 LEUKEMIA CHAPTER:4 1 BY Mrs. K.SHAILAJA., M. PHARM., LECTURER DEPT OF PHARMACY PRACTICE, SRM COLLEGE OF PHARMACY Leukemia A group of malignant disorders affecting the blood and blood-forming tissues of

More information

Blood transfusion. Dr. J. Potgieter Dept. of Haematology NHLS - TAD

Blood transfusion. Dr. J. Potgieter Dept. of Haematology NHLS - TAD Blood transfusion Dr. J. Potgieter Dept. of Haematology NHLS - TAD General Blood is collected from volunteer donors >90% is separated into individual components and plasma Donors should be: healthy, have

More information

Acute Immune Thrombocytopenic Purpura (ITP) in Childhood

Acute Immune Thrombocytopenic Purpura (ITP) in Childhood Acute Immune Thrombocytopenic Purpura (ITP) in Childhood Guideline developed by Robert Saylors, MD, in collaboration with the ANGELS team. Last reviewed by Robert Saylors, MD September 22, 2016. Key Points

More information

Chapter 3 Diseases of the Blood and Bloodforming Organs and Certain Disorders Involving the Immune Mechanism D50-D89

Chapter 3 Diseases of the Blood and Bloodforming Organs and Certain Disorders Involving the Immune Mechanism D50-D89 Chapter 3 Diseases of the Blood and Bloodforming Organs and Certain Disorders Involving the Immune Mechanism D50-D89 Presented by Jennifer Kurkulonis 1 FOUR MAJOR TYPES OF BLOOD CELLS White blood cells

More information

HEMATOLOGIC MORPHOLOGY- AECOM HEMATOLOGY COURSE

HEMATOLOGIC MORPHOLOGY- AECOM HEMATOLOGY COURSE Log Out Help current login :lcytryn@montefiore.org HEMATOLOGIC MORPHOLOGY- AECOM HEMATOLOGY COURSE Lawrence Cytryn, M.D. - Course Director 1998 Edward Burns, M.D. Images used by permission within AECOM

More information

Abnormal blood counts in children Dr Tina Biss Consultant Paediatric Haematologist Newcastle upon Tyne Hospitals NHS Foundation Trust

Abnormal blood counts in children Dr Tina Biss Consultant Paediatric Haematologist Newcastle upon Tyne Hospitals NHS Foundation Trust Abnormal blood counts in children Dr Tina Biss Consultant Paediatric Haematologist Newcastle upon Tyne Hospitals NHS Foundation Trust Regional Paediatric Specialty Trainees teaching 4 th July 2017 Scope

More information

Collect and label sample according to standard protocols. Gently invert tube 8-10 times immediately after draw. DO NOT SHAKE. Do not centrifuge.

Collect and label sample according to standard protocols. Gently invert tube 8-10 times immediately after draw. DO NOT SHAKE. Do not centrifuge. Complete Blood Count CPT Code: CBC with Differential: 85025 CBC without Differential: 85027 Order Code: CBC with Differential: C915 Includes: White blood cell, Red blood cell, Hematocrit, Hemoglobin, MCV,

More information

Clinical & Laboratory Assessment

Clinical & Laboratory Assessment Clinical & Laboratory Assessment Dr Roger Pool NHLS & University of Pretoria Clinical Assessment (History) Anaemia ( haemoglobin) Dyspnoea (shortness of breath) Tiredness Angina Headache Clinical Assessment

More information

PATHOLOGY & PATHOPHYSIOLOGY

PATHOLOGY & PATHOPHYSIOLOGY PATHOLOGY & PATHOPHYSIOLOGY DISORDERS OF BLOOD DISORDERS OF BLOOD Disorders of Blood Infections Tumours Nutritional disorders Coagulation disorders Congenital disorders Septicaemia Leukemia Iron deficiency

More information

7 Omar Abu Reesh. Dr. Ahmad Mansour Dr. Ahmad Mansour

7 Omar Abu Reesh. Dr. Ahmad Mansour Dr. Ahmad Mansour 7 Omar Abu Reesh Dr. Ahmad Mansour Dr. Ahmad Mansour -Leukemia: neoplastic leukocytes circulating in the peripheral bloodstream. -Lymphoma: a neoplastic process in the lymph nodes, spleen or other lymphatic

More information

Index. Note: Page numbers of article numbers are in boldface type.

Index. Note: Page numbers of article numbers are in boldface type. Index Note: Page numbers of article numbers are in boldface type. A Abdomen, acute, as cancer emergency, 381 399 in cancer patients, etiologies unique to, 390 392 in perforation, 388 surgery of, portal

More information

MEDICAL COVERAGE GUIDELINES ORIGINAL EFFECTIVE DATE: 08/19/14 SECTION: DRUGS LAST REVIEW DATE: LAST CRITERIA REVISION DATE: ARCHIVE DATE:

MEDICAL COVERAGE GUIDELINES ORIGINAL EFFECTIVE DATE: 08/19/14 SECTION: DRUGS LAST REVIEW DATE: LAST CRITERIA REVISION DATE: ARCHIVE DATE: RITUXAN (rituximab) Coverage for services, procedures, medical devices and drugs are dependent upon benefit eligibility as outlined in the member's specific benefit plan. This Medical Coverage Guideline

More information

Pathology of Hematopoietic and Lymphoid tissue

Pathology of Hematopoietic and Lymphoid tissue CONTENTS Pathology of Hematopoietic and Lymphoid tissue White blood cells and lymph nodes Quantitative disorder of white blood cells Reactive lymphadenopathies Infectious lymphadenitis Tumor metastasis

More information

Aplastic anamia & Sideroblastic anemia

Aplastic anamia & Sideroblastic anemia Hematology Lecture 7 كلية التقنيات الصحية والطبية قسم التحليالت المرضية Aplastic anamia & Sideroblastic anemia اإلعداد: ظفر جبار دهاق فؤاد APLASTIC ANEMIA What is Aplastic anemia? Aplastic anemia is a

More information

SAUDI FELLOWSHIP TRAINING PROGRAM. Adult Haematology. Final Written Examination 2019

SAUDI FELLOWSHIP TRAINING PROGRAM. Adult Haematology. Final Written Examination 2019 SAUDI FELLOWSHIP TRAINING PROGRAM Adult Haematology Final Written Examination 2019 Examination Format: A. The Saudi fellowship specialty final written examination shall consist of one paper with 80-120

More information

1 Introduction. 1.1 Cancer. Introduction

1 Introduction. 1.1 Cancer. Introduction Introduction 1 1.1 Cancer 1 Introduction Cancer is the most precarious disease characterized by uncontrolled proliferation of cells without any physiological demands of the organism. Cancer may be defined

More information

Introduction to Haematology. Prof Roger Pool Department of Haematology University of Pretoria

Introduction to Haematology. Prof Roger Pool Department of Haematology University of Pretoria Introduction to Haematology Prof Roger Pool Department of Haematology University of Pretoria Suggested reading Haematology at a Glance Atul Mehta & Victor Hoffbrand Second Edition Published by Blackwell

More information

Year 2003 Paper two: Questions supplied by Tricia

Year 2003 Paper two: Questions supplied by Tricia QUESTION 65 A 36-year-old man presents in a post-ictal state after an observed generalised seizure. Full blood investigation shows: haemoglobin 0 g/l [128-175] mean corpuscular volume (MCV) 106 fl [80-7]

More information

Haemostasis & Coagulation disorders Objectives:

Haemostasis & Coagulation disorders Objectives: Haematology Lec. 1 د.ميسم مؤيد علوش Haemostasis & Coagulation disorders Objectives: - Define haemostasis and what are the major components involved in haemostasis? - How to assess the coagulation status?

More information

WISKOTT-ALDRICH SYNDROME. An X-linked Primary Immunodeficiency

WISKOTT-ALDRICH SYNDROME. An X-linked Primary Immunodeficiency WISKOTT-ALDRICH SYNDROME An X-linked Primary Immunodeficiency WHAT IS WISKOTT ALDRICH SYNDROME? Wiskott-Aldrich Syndrome (WAS) is a serious medical condition that causes problems both with the immune system

More information

WBCs Disorders 1. Dr. Nabila Hamdi MD, PhD

WBCs Disorders 1. Dr. Nabila Hamdi MD, PhD WBCs Disorders 1 Dr. Nabila Hamdi MD, PhD ILOs Compare and contrast ALL, AML, CLL, CML in terms of age distribution, cytogenetics, morphology, immunophenotyping, laboratory diagnosis clinical features

More information

Dr. Rai Muhammad Asghar Associate Professor Head of Pediatric Department Rawalpindi Medical College

Dr. Rai Muhammad Asghar Associate Professor Head of Pediatric Department Rawalpindi Medical College Dr. Rai Muhammad Asghar Associate Professor Head of Pediatric Department Rawalpindi Medical College AN APPROACH TO BLEEDING DISORDERS NORMAL HEMOSTASIS After injury, 3 processes halt bleeding Vasoconstriction

More information

Clinical Utility. Clinical Utility of the Automated IG-Count Xavier Troussard

Clinical Utility. Clinical Utility of the Automated IG-Count Xavier Troussard 5. Clinical Utility Clinical Utility of the Automated IG-Count Xavier Troussard Introduction Quantitative analysis of immature granulocytes (IG) is useful for the optimal clinical and biological management

More information

78 The Power of Peripheral Blood Smears-Apparent Diagnostic Clues (Part 1) Gene Gulati PhD, SH(ASCP)

78 The Power of Peripheral Blood Smears-Apparent Diagnostic Clues (Part 1) Gene Gulati PhD, SH(ASCP) 78 The Power of Peripheral Blood Smears-Apparent Diagnostic Clues (Part 1) Gene Gulati PhD, SH(ASCP) 2011 Annual Meeting Las Vegas, NV AMERICAN SOCIETY FOR CLINICAL PATHOLOGY 33 W. Monroe, Ste. 1600 Chicago,

More information

ACGME Program Requirements for Graduate Medical Education in Pediatric Hematology-Oncology

ACGME Program Requirements for Graduate Medical Education in Pediatric Hematology-Oncology ACGME Program Requirements for Graduate Medical Education in Pediatric Hematology-Oncology ACGME approved: June 27, 2006; effective: July 1, 2007 ACGME approved focused revision: September 30, 2012; effective:

More information

What is a hematological malignancy? Hematology and Hematologic Malignancies. Etiology of hematological malignancies. Leukemias

What is a hematological malignancy? Hematology and Hematologic Malignancies. Etiology of hematological malignancies. Leukemias Hematology and Hematologic Malignancies Cancer of the formed elements of the blood What is a hematological malignancy? A hematologic malignancy is a malignancy (or cancer) of any of the formed elements

More information

Saudi Fellowship Training Program. Final Written Examination of Adult Hematology 2018

Saudi Fellowship Training Program. Final Written Examination of Adult Hematology 2018 Saudi Fellowship Training Program Final Written Examination of Adult Hematology 2018 Objectives: Determine the quantity and quality of a hematologist s knowledge base ranked as competent, so that the individual

More information

Diseases Of The Blood

Diseases Of The Blood Diseases Of The Blood DR. Associate Professor Of Pathology Faculty Of Medicine Ain Shams University Red Blood Cells and Anemia RBC=4-6 million/mm 2 Hb=12-18 g/dl Oxygen Carrying Molecule Hemoglobin Tetramer:

More information

Chapter 11. Lecture and Animation Outline

Chapter 11. Lecture and Animation Outline Chapter 11 Lecture and Animation Outline To run the animations you must be in Slideshow View. Use the buttons on the animation to play, pause, and turn audio/text on or off. Please Note: Once you have

More information

GUIDELINES FOR THE TRANSFUSION OF BLOOD COMPONENTS

GUIDELINES FOR THE TRANSFUSION OF BLOOD COMPONENTS CHILDREN S HOSPITALS AND CLINICS OF MINNESOTA Introduction: GUIDELINES FOR THE TRANSFUSION OF BLOOD COMPONENTS These guidelines have been developed in conjunction with the hospital Transfusion Committee.

More information

2013 Pathology Student

2013 Pathology Student About this guide If you re reading this introduction, it means you are probably either a) covering hematopathology in your pathology class right now, or b) studying for boards. Either way, you ve come

More information

MYELODYSPLASTIC AND MYELOPROLIFERATIVE

MYELODYSPLASTIC AND MYELOPROLIFERATIVE MYELODYSPLASTIC AND MYELOPROLIFERATIVE DISORDERS Pediatric Hemato-Oncology Division Medical Faculty University of Sumatera Utara 1 MYELODYSPLASIA SYNDROME A group of disorder defect in hematopoetic cell

More information

Preferred Clinical Services for Leading Age Florida August 26-27, 2015

Preferred Clinical Services for Leading Age Florida August 26-27, 2015 DIAGNOSIS CODING ESSENTIALS FOR LONG-TERM CARE: CHAPTER 3, D CODES DISEASES OF THE BLOOD AND BLOOD-FORMING ORGANS AND CERTAIN DISORDERS INVOLVING THE IMMUNE MECHANISM Preferred Clinical Services for Leading

More information

Recommended Timing for Transplant Consultation

Recommended Timing for Transplant Consultation REFERRAL GUIDELINES Recommended Timing for Transplant Consultation Published jointly by the National Marrow Donor Program /Be The Match and the American Society for Blood and Marrow Transplantation BeTheMatchClinical.org

More information

If unqualified, Complete remission is considered to be Haematological complete remission

If unqualified, Complete remission is considered to be Haematological complete remission Scroll right to see the database codes for Disease status and Response Diagnosis it refers to Disease status or response to treatment AML ALL CML CLL MDS or MD/MPN or acute leukaemia secondary to previous

More information

Pathology of Hematopoietic and Lymphoid tissue

Pathology of Hematopoietic and Lymphoid tissue Pathology of Hematopoietic and Lymphoid tissue Peerayut Sitthichaiyakul, M.D. Department of Pathology and Forensic Medicine Faculty of Medicine, Naresuan University CONTENTS White blood cells and lymph

More information

2010 Hematopoietic and Lymphoid ICD-O Codes - Alphabetical List THIS TABLE REPLACES ALL ICD-O-3 Codes

2010 Hematopoietic and Lymphoid ICD-O Codes - Alphabetical List THIS TABLE REPLACES ALL ICD-O-3 Codes Acute basophilic leukemia 9870/3 Acute biphenotypic leukemia [OBS] 9805/3 Acute erythroid leukemia 9840/3 Acute megakaryoblastic leukemia 9910/3 Acute monoblastic and monocytic leukemia 9891/3 Acute myeloid

More information

2012 Hematopoietic and Lymphoid ICD-O Codes - Numerical List THIS TABLE REPLACES ALL ICD-O-3 Codes

2012 Hematopoietic and Lymphoid ICD-O Codes - Numerical List THIS TABLE REPLACES ALL ICD-O-3 Codes Malignant lymphoma, NOS 9590/3 Non-Hodgkin lymphoma, NOS 9591/3 B-cell lymphoma, unclassifiable, with features intermediate between diffuse large B-cell lymphoma and classical Hodgkin lymphoma 9596/3 Primary

More information

Immunodeficiency. By Dr. Gouse Mohiddin Shaik

Immunodeficiency. By Dr. Gouse Mohiddin Shaik Immunodeficiency By Dr. Gouse Mohiddin Shaik Immunodeficieny Immunodeficiency is failure of immune system to protect against disease or malignency Immunodeficiency is of two types Primary Secondary immunodeficiency

More information

If unqualified, Complete remission is considered to be Haematological complete remission

If unqualified, Complete remission is considered to be Haematological complete remission Scroll right to see the database codes for Disease status and Response Diagnosis it refers to Disease status or response to treatment AML ALL CML CLL MDS or MD/MPN or acute leukaemia secondary to previous

More information

Pediatric Hematology-Oncology

Pediatric Hematology-Oncology Pediatric Hematology-Oncology Content Outline In-Training, Initial Certification, and Maintenance of Certification Exams Effective for exams administered beginning April 1, 2019 THE AMERICAN BOARD of PEDIATRICS

More information

Year 2002 Paper two: Questions supplied by Jo 1

Year 2002 Paper two: Questions supplied by Jo 1 Year 2002 Paper two: Questions supplied by Jo 1 Question 70 A 25 year old previously well male student presents with recent exertional dyspnoea, epistaxis and bruising. There is no history of medication,

More information

FBC CASES Vernon Louw Clinical Haematology 2010

FBC CASES Vernon Louw Clinical Haematology 2010 FBC CASES Vernon Louw Clinical Haematology 2010 FOR EACH OF THE FOLLOWING PATIENTS, SELECT THE MOST LIKELY FINDING FROM THE ANALYSIS OF THE PERIPHERAL BLOOD. A patient with infectious mononucleosis. A

More information

Disorders of Blood Cells & Blood Coagulation

Disorders of Blood Cells & Blood Coagulation Disorders of Blood Cells & Blood Coagulation HIHIM 409 WBC count RBC count WBC differential Hemoglobin (HGB) Hematocrit (HCT) % of volume occupied by RBCs CBC Red cell indices Mean cell volume (MCV) average

More information

Candidates must answer ALL questions

Candidates must answer ALL questions Time allowed: Three hours. Part 1 examination Haematology: First paper Tuesday 22 March 2016 Candidates must answer ALL questions Question 1: General Haematology A 16 year old non-european is referred

More information

The Complete Blood Count

The Complete Blood Count The Complete Blood Count (Cartesian Thinking at Its Best) A SEM Image of Normal Human Blood Laurie Larsson February 22, 2010 Anatomy and Philology II Dr. Danil Hammoudi Introduction A complete blood count

More information

Platelet Disorders. By : Saja Al-Oran

Platelet Disorders. By : Saja Al-Oran Platelet Disorders By : Saja Al-Oran Introduction The platelet arise from the fragmentation of the cytoplasm of megakaryocyte in the bone marrow. circulate in the blood as disc-shaped anucleate particles

More information

3/5/2013. Hematopoiesis: Red and white marrow. Hematopoiesis. Bone marrow aspirate and core biopsy. Gartner, Color Textbook of Histology, 3 rd Edition

3/5/2013. Hematopoiesis: Red and white marrow. Hematopoiesis. Bone marrow aspirate and core biopsy. Gartner, Color Textbook of Histology, 3 rd Edition Hematopoiesis Hematopoiesis: Red and white marrow Bone marrow aspirate and core biopsy Gartner, Color Textbook of Histology, 3 rd Edition 1 reticulocytes elliptocytes schistocytes spheroctyes target cells

More information

The Lymphatic System and Body Defenses

The Lymphatic System and Body Defenses PowerPoint Lecture Slide Presentation by Patty Bostwick-Taylor, Florence-Darlington Technical College The Lymphatic System and Body Defenses 12PART B Adaptive Defense System: Third Line of Defense Immune

More information

Blood Components & Indications for Transfusion. Neda Kalhor

Blood Components & Indications for Transfusion. Neda Kalhor Blood Components & Indications for Transfusion Neda Kalhor Blood products Cellular Components: Red blood cells - Leukocyte-reduced RBCs - Washed RBCs - Irradiated RBCs Platelets - Random-donor platelets

More information

Leukocytosis - Some Learning Points

Leukocytosis - Some Learning Points Leukocytosis - Some Learning Points Koh Liang Piu Department of Hematology-Oncology National University Cancer Institute National University Health System Objectives of this talk: 1. To provide some useful

More information

BSc in Medical Sciences with HAEMATOLOGY

BSc in Medical Sciences with HAEMATOLOGY BSc in Medical Sciences with HAEMATOLOGY Introduction The BSc in Medical Sciences with Haematology is directed at students who have an interest in the scientific basis of medical practice. While directed

More information

MOC HEM - General Hematopathology (Mandatory 50-Question Module)

MOC HEM - General Hematopathology (Mandatory 50-Question Module) MOC HEM - General Hematopathology (Mandatory 50-Question Module) acute monoblastic/monocytic leukemia infectious mononucleosis adult T cell leukemia/lymphoma in situ follicular lymphoma ALL; phenotypes

More information

Bio& 242 Unit 3 / Lecture 1

Bio& 242 Unit 3 / Lecture 1 Bio& 242 Unit 3 / Lecture 1 Major Functions of Blood The body contains 4 to 6 liters of blood with an average ph of 7.35 to 7.45. Functions include: Transport Oxygen, Carbon Dioxide, Nutrients, Hormones,

More information

MOC HEM - General Hematopathology (Mandatory 50-Question Module)

MOC HEM - General Hematopathology (Mandatory 50-Question Module) MOC HEM - General Hematopathology (Mandatory 50-Question Module) acute monoblastic/monocytic leukemia infectious mononucleosis adult T cell leukemia/lymphoma in situ follicular lymphoma ALL; phenotypes

More information

Lahey Clinic Internal Medicine Residency Program: Curriculum for Hematology

Lahey Clinic Internal Medicine Residency Program: Curriculum for Hematology Lahey Clinic Internal Medicine Residency Program: Curriculum for Hematology Faculty representative: Neil Weiner, MD Resident representative: Guiherme Rabinowits, MD Revision date: February 28, 2006 Goals

More information

Extramedullary precursor T-lymphoblastic transformation of CML at presentation

Extramedullary precursor T-lymphoblastic transformation of CML at presentation Extramedullary precursor T-lymphoblastic transformation of CML at presentation Neerja Vajpayee, Constance Stein, Bernard Poeisz & Robert E. Hutchison Clinical History 30 year old man presented to the emergency

More information

Appendix 6: Indications for adult allogeneic bone marrow transplant in New Zealand

Appendix 6: Indications for adult allogeneic bone marrow transplant in New Zealand Appendix 6: Indications for adult allogeneic bone marrow transplant in New Zealand This list provides indications for the majority of adult BMTs that are performed in New Zealand. A small number of BMTs

More information

PNH Glossary of Terms

PNH Glossary of Terms AA Absolute neutrophil count Alendronate Allergen ALT Anemia Antibodies Anticoagulant Anticoagulation Antigen Antithymocyte globulin (ATG) Aplastic Aplastic anemia Band Bilirubin Blast cells Bone marrow

More information

Rory McCulloch. Specialty Trainee Haematology Royal Devon & Exeter Hospital

Rory McCulloch. Specialty Trainee Haematology Royal Devon & Exeter Hospital Rory McCulloch Specialty Trainee Haematology Royal Devon & Exeter Hospital Anaemia 1 Haematological disorders Anaemia 2 Non-haematological disorders Substrates: Iron, folate, vitamin B12 Red cell mass

More information

University: Alexandria Faculty : Medicine Program Specifications (Academic year: 2015)

University: Alexandria Faculty : Medicine Program Specifications (Academic year: 2015) الهيئة القومية لضمان جودة التعليم واالعتماد University: Alexandria Faculty : Medicine Program Specifications (Academic year: 2015) الهيئة القومية لضمان جودة التعليم واالعتماد A. Basic Information: 1. Program

More information

GP Referral Guidelines. for. South Wales Cancer Network. Document Control Sheet. Specialty/Project Haematological Site Specific Group

GP Referral Guidelines. for. South Wales Cancer Network. Document Control Sheet. Specialty/Project Haematological Site Specific Group GP Referral Guidelines for South Wales Cancer Network Document Control Sheet Organisation South Wales Cancer Network Specialty/Project Haematological Site Specific Group Document Title GP Referral Guidelines

More information

Beyond the CBC Report: Extended Laboratory Testing in the Evaluation for Hematologic Neoplasia Disclosure

Beyond the CBC Report: Extended Laboratory Testing in the Evaluation for Hematologic Neoplasia Disclosure Beyond the CBC Report: Extended Laboratory Testing in the Evaluation for Hematologic Neoplasia Disclosure I am receiving an honorarium from Sysmex for today s presentation. 1 Determining the Etiology for

More information

MYELODYSPLASTIC SYNDROMES: A diagnosis often missed

MYELODYSPLASTIC SYNDROMES: A diagnosis often missed MYELODYSPLASTIC SYNDROMES: A diagnosis often missed D R. EMMA W YPKEMA C O N S U LTA N T H A E M AT O L O G I S T L A N C E T L A B O R AT O R I E S THE MYELODYSPLASTIC SYNDROMES DEFINITION The Myelodysplastic

More information

WHO Classification. B-cell chronic lymphocytic leukemia/small T-cell granular lymphocytic leukemia

WHO Classification. B-cell chronic lymphocytic leukemia/small T-cell granular lymphocytic leukemia Blood Malignancies-II Prof. Dr. Herman Hariman, a Ph.D, SpPK (KH). Prof. Dr. Adikoesoema Aman, SpPK (KH) Dept. of Clinical Pathology, School of Medicine, University of North Sumatra WHO classification

More information

Osteosclerotic Myeloma (POEMS Syndrome)

Osteosclerotic Myeloma (POEMS Syndrome) Osteosclerotic Myeloma (POEMS Syndrome) Osteosclerotic Myeloma (POEMS Syndrome) Synonyms Crow-Fukase syndrome Multicentric Castleman disease Takatsuki syndrome Acronym coined by Bardwick POEMS Scheinker,

More information

Group of malignant disorders of the hematopoietic tissues characteristically associated with increased numbers of white cells in the bone marrow and

Group of malignant disorders of the hematopoietic tissues characteristically associated with increased numbers of white cells in the bone marrow and Group of malignant disorders of the hematopoietic tissues characteristically associated with increased numbers of white cells in the bone marrow and / or peripheral blood Classified based on cell type

More information

Autoimmune lymphoproliferative syndrome (ALPS)

Autoimmune lymphoproliferative syndrome (ALPS) ALPS Autoimmune lymphoproliferative syndrome (ALPS) Information for families hello@piduk.org 0800 987 8986 www.piduk.org About this leaflet This leaflet is designed to help answer the questions families

More information

Combinations of morphology codes of haematological malignancies (HM) referring to the same tumour or to a potential transformation

Combinations of morphology codes of haematological malignancies (HM) referring to the same tumour or to a potential transformation Major subgroups according to the World Health Organisation (WHO) Classification Myeloproliferative neoplasms (MPN) Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB or

More information

a resource for physicians Recommended Referral Timing for Stem Cell Transplant Evaluation

a resource for physicians Recommended Referral Timing for Stem Cell Transplant Evaluation a resource for physicians Recommended Referral Timing for Stem Cell Transplant Evaluation This resource has been developed to help guide you regarding the appropriate timing and conditions for a referral

More information

Dr Kirsten Herbert. Dr Melita Kenealy. MBBS(Hons) FRCPA FRACP. Common Blood Tests

Dr Kirsten Herbert. Dr Melita Kenealy. MBBS(Hons) FRCPA FRACP. Common Blood Tests Common Blood Tests Your Haematologist may order numerous blood and urine tests to help diagse or manage your condition. Listed below are some of the more common tests that can be ordered in a haematology

More information

Hematology 101. Rachid Baz, M.D. 5/16/2014

Hematology 101. Rachid Baz, M.D. 5/16/2014 Hematology 101 Rachid Baz, M.D. 5/16/2014 Florida 101 Epidemiology Estimated prevalence 8,000 individuals in U.S (compare with 80,000 MM patients) Annual age adjusted incidence 3-8/million-year 1 More

More information

Overview of Aplastic Anemia. Overview of Aplastic Anemia. Epidemiology of aplastic anemia. Normal hematopoiesis 10/6/2017

Overview of Aplastic Anemia. Overview of Aplastic Anemia. Epidemiology of aplastic anemia. Normal hematopoiesis 10/6/2017 Overview of Aplastic Anemia Overview of Aplastic Anemia Peter Westervelt, MD, PhD Professor of Medicine Chief, BMT/Leukemia Section Washington University School of Medicine Epidemiology Normal hematopoiesis

More information

Bone marrow failure. By Zahraa Nasooh Al_Saaty

Bone marrow failure. By Zahraa Nasooh Al_Saaty Bone marrow failure By Zahraa Nasooh Al_Saaty Pancytopenia : Pancytopenia describes a reduction in the blood count of all the major cell lines-red cells,white cell and platelets. It has several causes

More information