Spleen and other reticulo endothelia tissues ; splenic strucure and functions by AO Shittu PDF free download

Topics: SPLENIC ANATOMY, SPLENIC STRUCTURE, SPLENIC CIRCULATION, PATHOLOGIC SPLEEN, SPLENECTOMY

Topics: Myeloid maturation, stem cell, Acute leukaemia

Topics: PCV Reading, Drabkin solution, red blood cell count, white blood cell count, platelet count, red cell absolute indicies, sickling test, haemoglobin electrophoresis, Coomb's test, haemostasis, blood grouping, blood bag, copper sulphate solution, leishman stain, EDTA

Topics: Spleen, VISCERAL, DIAPHRAGMATIC SURFACE, Gastrosplenic ligarment, Splenecolic ligarment, Splenorenal ligarment, Phrenicocolic ligarment, gastrosplenic ligament

Topics: Haemopoiesis, anaemia, Erythropoiesis, Hypochromic anaemia, iron oveload, Megaloblastic anaemia, macrocytic anaemia, Haemolytic anaemia, granulocytes, monocytes, lymphocytes, spleen, haematological malignancy, Acute myeloid leukaemia, Chronic myeloid leukaemia, Myeloproliferative disease, myeloid leukaemia, Myelodysplasia, chronic lymphoid leukaemia, Hodgkin lymphoma, Non-Hodgkin lymphoma, Multiple myeloma, Aplastic anaemia, bone marrow failure, Stem cell transplantation, Platelets, blood coagulation, haemostasis, Bleeding disorders, platelet abnormalities, vascular abnormalities, Coagulation disorders, Thrombosis, Blood transfusion, Pregnancy haematology, neonatal haematology

Topics: reagent, Leishman Stain, Giemsas Stain, Packed Cell Volume

Topics: Deficiency of vitamin K, Liver diseases, Disseminated Intravascular Coagulopathy, Severe sepsis, HAEMORRHAGIC DISEASE OF NEW BORN, LIVER DISEASE, ANTI PHOSPHO LIPID SYNDROME

Topics: erythropoietin.Inhibition of erythropoiesi, iron metabolism, Haematological features of Anaemia of chronic disease

Topics: unfractionated heparin, Low Molecular Weight Heparin, Heparin Therapy, Oral Anticoagulants, Warfarin Metabolism, Newer Anticoagulants, Fibrinolytic Drugs, Thrombolytic agents

Topics: Haemostatic mechanism, blood vessels, superficial bleeding, petechiae, ecchymosis, non thrombocytopenic purpura, senile purpura, Hereditary haemorrhagic telangiectasia, Osler-Rendu-Weber syndrome, CONNECTIVE TISSUE DISORDERS, Ehlers-Danlos syndrome, Pseudoxanthoma elasticum, Osteogenesis imperfecta, Marfan’s syndrome, ALLERGIC PURPURA, Henoch-Schoenlin purpura, PSYCHOGENIC PURPURA, INFECTIOUS PURPURA, PLATELET ADHESSION, thrombocytopathies, Bernard-Soulier syndrome, Platelet type von-Willibrand, Montreal platelet syndrome, IMMUNE MEDIATED THRONBOCYTOPENIA, Auto Immune Thrombocytopenia, BONE MARROW SUPPRESSION, Thrombotic thrombocytopenic purpura, Haemolytic uraemic syndrome

Topics: Karl Landsteiner, AB0 blood grouping system, Blood group A, Blood group B, Blood group AB, Blood group 0, Rh factor blood grouping system, Blood group notation, Blood transfusion

Topics: Bone marrow failure syndrome, ACQUIRED Bone marrow failure, PANCYTOPAENIA, Aplastic anaemia, IDIOSYNCRATIC ACQUIRED APLASTIC ANAEMIA, Stable aplastic anaemia, fluctuating aplasia, Progressive aplasia, unstable aplasia, Bone marrow trephine, Ant ilymphocyte globulin, Cyclosporin, androgen, Allogeneic bone marrow transplantation, peripheral blood stem cell

Topics: Burkitt’s tumour, starry sky

Topics: Pure red cell aplasia, Diamond-Blackfan anaemia, Congenital pure red cell aplasia, Paroxysmal nocturnal haemoglobinuria

Topics: neutrophilia, EOSINOPHILIA, Hypereosinophilc Syndrome, BASOPHILIA, Monocytosis, Pelger-Huet anomaly, Neutrophil hypersegmentation, May-Hegglin anomaly, Alder’s anomaly, Chediak-Higashi syndrome, Hypersegmentation, DISORDERS OF DENDRITIC CELLS, Langerhan’s cell histiocytosis, Haemophagocytic lymphohistiocytosis

Topics: Polymorphonuclear phagocyte, Mononuclear phagocyte, Granulopoiesis, Neutrophil, MYELOBLAST, Promyelocyte, Myelocyte, Metamyelocyte, Neutrophil maturation, Bone marrow nucleated cells, Eosinophils, basophil cells, mast cells, Monocytes, Macrophages

Topics: IMMUNE HAEMOLYTIC ANAEMIAS, AUTO IMMUNE HAEMOLYTIC ANAEMIAS, immunoglobulin, Red cell destructionComplement mediated destruction, cold AUTO IMMUNE HAEMOLYTIC ANAEMIA, PAROXYMAL COLD HAEMOGLOBINURIA, ALLO IMMUNE HAEMOLYTIC ANAEMIA, DRUG INDUCED HAEMOLYTIC ANAEMIA, RED CELL FRAGMENTATION SYNDROME, MACRO ANGIOPATHIC HAEMOLYTIC ANAEMIA, MICRO ANGIOPATHIC HAEMOLYTIC ANAEMIAS, MARCH HAEMOGLOBINURIA, PAROXYSMAL NOCTURNAL HAEMOGLOBINURA, glycosylphosphatidylinositol

Topics: ENZYMOPATHIES, GLYCOLYSIS, Glutathione, NUCLEOSIDE METABOLISM, G6PD DEFICIENCY, ACUTE HAEMOLYTIC ANAEMIA, Chronic haemolytic anaemia, PYRUVATE KINASE DEFICIENCY

Topics: Immune Hemolytic disorder, Auto-immune Hemolytic anemia, Cold AIHA, Paroxysmal Cold hemoglobinuria, Allo-immune Hemolytic anemia, immune Thrombocytopenic purpura, Evan's syndrome, IMMUNE HEMOLYTIC ANEMIA, Antibody-mediated hemolysis, AUTOIMMUNE HEMOLYTIC ANEMIA, Red cell destruction, cold AIHA syndrome, warm AIHA, ALLOIMMUNE HEMOLYTIC ANEMIA, DRUG-INDUCED HEMOLYTIC ANEMIA, ACQUIRED NON-IMMUNE HEMOLYTIC ANEMIA, INTRAVASCULAR HEMOLYSIS, BLACK WATER FEVER, HEMOPHAGOCYTIC SYNDROME, FRAGMENTATION HEMOLYSIS, MECHANICAL HEMOLYTIC ANEMIA, RED CELL FRAGMENTATION SYNDROME, MICROANGIOPATHIC HEMOLYTIC ANEMIA, HEMOLYTIC UREMIC SYNDROME, THROMBOTIC THROMBOCYTOPENIC PURPURA

Topics: Membrane disorders, MEMBRANOPATHIES, Red cell membrane, hereditary membrane disorders, Hereditary SpherocytosisAplastic crisis, Acute sequestration crisis, Megaloblastic crisis, Gallstones, Hereditary Elliptocytosis, Familial Lecithin-Cholesterol Acyl transferase Deficiency, Echinocytosis, Acanthocytosis, Abetalipoproteinaemia