Practical Pediatric HematologyAnupam Sachdeva Evidence-based medicine is the need of the hour. Every pediatrician strives for perfection is his or her practice. These are exciting times for Pediatric Hematology and Oncology. Major advances during the past decade in the field have enhanced the understanding and significantly influenced the management and outcome of many of these chronic and fatal diseases affecting children. While opportunities to learn decrease after one leaves the medical school, science keeps evolving. Keeping this in mind, Indian Academy of Pediatrics (IAP) envisaged starting specialty training under its plan of action 2006. Such trainings keep professional and residents updated about newly launched technologies and other advancements. This book is well illustrated and has many pictures and diagrams for the quick understanding of readers. This will be of use not only to the postgraduates of pediatrics but also will be of immense use to a general pediatrician as a ready-reckoner to be kept on the desk. |
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Page xxii
... Syndrome in Children Infections 233 Viral Illnesses with Marked Hematologic Sequel 235 Hematologic Changes Associated with Specific Infections in the Tropics 238 Hyper-reactive Malarial Splenomegaly Syndrome 240 Clinical Features 241 ...
... Syndrome in Children Infections 233 Viral Illnesses with Marked Hematologic Sequel 235 Hematologic Changes Associated with Specific Infections in the Tropics 238 Hyper-reactive Malarial Splenomegaly Syndrome 240 Clinical Features 241 ...
Page 1
... syndrome (AIDS) c. Peripheral destruction of cells i. Immunoneutropenia ii. Idiopathic thrombocytopenic purpura (ITP) iii. Immune hemolytic anemia, singly or in combination iv. Sequestration of cells (e.g. hypersplenism). Vikas Dua ...
... syndrome (AIDS) c. Peripheral destruction of cells i. Immunoneutropenia ii. Idiopathic thrombocytopenic purpura (ITP) iii. Immune hemolytic anemia, singly or in combination iv. Sequestration of cells (e.g. hypersplenism). Vikas Dua ...
Page 3
... syndrome, giant azurophilic granules are present in lymphocytes, whereas granulocytes contain very large irregular granules. Hemoglobin and Hematocrit Values Hemoglobin and hematocrit values relate to the number and content of ...
... syndrome, giant azurophilic granules are present in lymphocytes, whereas granulocytes contain very large irregular granules. Hemoglobin and Hematocrit Values Hemoglobin and hematocrit values relate to the number and content of ...
Page 9
... syndrome • May Hegglin anomaly and other MYH-9–related diseases • Swiss cheese platelet syndrome • Montreal platelet syndrome • Gray platelet syndrome • Various mucopolysaccharidosis. Normal Size (MPV Normal) Conditions in which marrow ...
... syndrome • May Hegglin anomaly and other MYH-9–related diseases • Swiss cheese platelet syndrome • Montreal platelet syndrome • Gray platelet syndrome • Various mucopolysaccharidosis. Normal Size (MPV Normal) Conditions in which marrow ...
Page 11
... syndrome, and malignancy. Eosinopenia is associated with corticosteroid therapy, adrenocortical hyperfunction ... syndromes • Unstable hemoglobins • HMP shunt abnormalities (G6PD deficiency) • Asplenia. Fig. 1.3: Target cells (For color ...
... syndrome, and malignancy. Eosinopenia is associated with corticosteroid therapy, adrenocortical hyperfunction ... syndromes • Unstable hemoglobins • HMP shunt abnormalities (G6PD deficiency) • Asplenia. Fig. 1.3: Target cells (For color ...
Contents
Chapter21 | 156 |
Chapter22 | 165 |
Chapter23 | 178 |
Chapter24 | 181 |
Chapter25 | 199 |
Chapter26 | 208 |
Chapter27 | 232 |
Chapter28 | 247 |
Chapter09 | 69 |
Chapter10 | 75 |
Chapter11 | 85 |
Chapter12 | 90 |
Chapter13 | 97 |
Chapter14 | 115 |
Chapter15 | 120 |
Chapter16 | 125 |
Chapter17 | 130 |
Chapter18 | 144 |
Chapter19 | 148 |
Chapter20 | 153 |
Chapter29 | 259 |
Chapter30 | 262 |
Chapter31 | 266 |
Chapter32 | 272 |
Chapter33 | 281 |
Chapter34 | 289 |
Chapter35 | 298 |
Chapter36 | 305 |
Chapter37 | 309 |
Index | 313 |
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Common terms and phrases
abnormalities acid activity acute adults antibodies anticoagulant antigen aplastic anemia APTT assay associated bleeding blood loss bone marrow transplantation catheter cause chemotherapy child childhood chronic clinical concentration congenital cytopenia decreased defects develop diagnosis disease disorders Disseminated intravascular coagulation donor dose drugs erythrocyte erythropoietin factor VIII ferritin fetal fibrin fibrinogen folate g/dl gene globin granulocytes Haematol hematocrit hematological hemoglobin hemolysis hemolytic anemia hemophilia hemorrhage heparin hepatitis immune increased India infants infection infusion inhibitor intravenous iron deficiency ischemic laboratory leukemia levels liver malignancy mutations myelodysplastic syndrome myeloid neonatal neutropenia newborn normal nutritional occur oral patients Pediatr peripheral plasma platelet platelet count platelet transfusion present preterm prophylaxis protein prothrombin red cell reticulocyte count risk serum severe splenectomy stem cell stroke studies syndrome Table thalassemia therapy thrombin thrombocytopenia thrombocytosis thrombosis tissue treatment usually venous viral virus vitamin