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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Alterations of Hematologic Function in Children Chapter 21
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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Acquired Disorders of Erythrocytes Iron deficiency anemia Most common blood disorder of infancy and childhood Lack of iron intake or blood loss Manifestations Irritability, decreased activity tolerance, weakness, and lack of interest in play Irritability, decreased activity tolerance, weakness, and lack of interest in play
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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Acquired Disorders of Erythrocytes Acquired congenital hemolytic anemia Hemolytic disease of the newborn (HDN) Alloimmune disease Alloimmune disease Maternal antibody directed against fetal antigens Maternal antibody directed against fetal antigens ABO incompatibility occurs in 20% to 25% of cases ABO incompatibility occurs in 20% to 25% of cases Rh incompatibility occurs in less than 10% Rh incompatibility occurs in less than 10% Also termed erythroblastosis fetalis Also termed erythroblastosis fetalis
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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Acquired Disorders of Erythrocytes Hemolytic disease of the newborn (HDN) Manifestations Anemia Anemia Hyperbilirubinemia Hyperbilirubinemia Icterus neonatorum Icterus neonatorum Kernicterus Kernicterus Glucose-6-phosphate dehydrogenase deficiency (G6PD) Glucose-6-phosphate dehydrogenase deficiency (G6PD)
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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Hemolytic Disease of the Newborn
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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Inherited Disorders of Erythrocytes Sickle cell disease Disorders characterized by the presence of an abnormal hemoglobin (HbS) Mutation causes valine to be replaced by glutamic acid Mutation causes valine to be replaced by glutamic acid Deoxygenation and dehydration cause the red cells to solidify and stretch into an elongated sickle shape
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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Inherited Disorders of Erythrocytes Sickle cell disease Sickle cell trait Child inherits HbS from one parent and HbA from another Child inherits HbS from one parent and HbA from another Can result in: Vaso-occlusive crisis (thrombotic crisis), aplastic crisis, sequestration crisis, and hyperhemolytic crisis Vaso-occlusive crisis (thrombotic crisis), aplastic crisis, sequestration crisis, and hyperhemolytic crisis Other forms Sickle cell-thalassemia disease and sickle cell-HbC disease Sickle cell-thalassemia disease and sickle cell-HbC disease
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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Sickle Cell Disease
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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Sickle Cell Disease
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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Sickle Cell Disease
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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Inherited Disorders of Erythrocytes Thalassemias Autosomal recessive disorders Synthesis of the globin chains of the hemoglobin molecule is slowed or defective Major—homozygous inheritance Minor—heterozygous inheritance
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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Inherited Disorders of Erythrocytes In alpha thalassemia, the alpha chains are affected; beta chains in beta thalassemia Beta-thalassemia minor Beta-thalassemia major (Cooley anemia) Life-threatening condition Life-threatening condition
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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Inherited Disorders of Erythrocytes Alpha trait Alpha-thalassemia minor Hemoglobin H disease Alpha-thalassemia major Fatal condition Fatal condition
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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Beta Thalassemia Major
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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Inherited Coagulation and Platelet Disorders Hemophilias Serious bleeding disorders Hemophilia A (factor VIII deficiency) von Willebrand disease von Willebrand disease Hemophilia B (factor IX deficiency) Hemophilia C (factor XI deficiency)
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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Antibody-Mediated Hemorrhagic Disease Idiopathic thrombocytopenic purpura Autoimmune or primary thrombocytopenic purpura Platelet destruction rate that exceeds production 70% with antecedent viral disease
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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Antibody-Mediated Hemorrhagic Disease Idiopathic thrombocytopenic purpura Manifestations of bruising and petechial rash Prognosis excellent with 80% regaining normal platelet counts within 6 months after onset
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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Leukemia Most common malignancy of childhood 80% to 85% are acute lymphoblastic leukemias (ALL); remainder acute myelogenous leukemia (AML) Result of ecogenetics Manifestations of pallor, fatigue, purpura, and fever Blast cell is hallmark of ALL
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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Leukemia
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Lymphoma Non-Hodgkin lymphoma (NHL) Nodular or diffuse Childhood NHL subdivided Large cell (histiocytic) Large cell (histiocytic) Lymphoblastic Lymphoblastic Small noncleaved cell (Burkitt or non-Burkitt) Small noncleaved cell (Burkitt or non-Burkitt)
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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Lymphoma Non-Hodgkin lymphoma (NHL) Etiology viral, chronic immunostimulation, congenital immunodeficiency syndromes, and genetics Manifestations specific to site involved Treatment of chemotherapy and radiation
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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Lymphoma Hodgkin lymphoma Rare in childhood Infectious mode of transmission Many children with Hodgkin lymphoma demonstrate a high antibody titer to Epstein- Barr virus (EBV) Manifestations of painless adenopathy, anorexia, malaise, fever, and weight loss Treatment by MOPP or ABVD
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Elsevier items and derived items © 2008 by Mosby, Inc., an affiliate of Elsevier Inc. Lymphoma
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Lymphoma
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