MCPHS PA Pathophys Exam 3 Hematopoietic & Lymphoid Systems Flashcards
Approx how many cells are produced by bone marrow every day?
100 billion making the Bone Marrow one of the most active organs in the body.
In adults most active marrow resides in the vertebrae, sternum, and ribs.
In children the marrow is more active in the long bones.
In fetus the spleen, liver, and lymphnode produce until birth.
What is the composition of blood in the body?
Approx 5.5L
55% Plasma
7% proteins
91% water
2% other solutes
45% Formed Elements
<1% Platelets
<1% Leukocytes
>99% Erythrocytes
What is Serum?
Part of blood which is similar in composition with plasma but excluding clotting factors of blood. (Plasma - Clotting factors = Serum)
What are the Characteristics of RBCs?
Biconcave disk
No Nucleus
4-6 Million
120 day Life Span
Transport O2 and CO
What are granulocytes?
Neutrophil
Eosinophil
Basophil
What are Agranulocytes?
Monocyte
Lymphocyte
What is Anemia?
A reduction in the Oxygen-transporting Capacity of blood resulting from a decrease in the red cell mass to subnormal levels.
What is the pathogenesis of Anemia?
Decrease in RBC circulation causing Anemia which is a decrease in O2 carrying capacity which leads to Tissue Hypoxia.
How does Anemia present?
Decreased Hematocrit (RBC/blood volume ratio)
Decreased Hemoglobin concentration
These correlate with the red cell mass except when there are changes in plasma volume caused by fluid retention or dehydration
What are the most useful red cell indices in Anemia?
Mean cell volume: Avg. volume of a RBC (macro microcytic)
Mean cell hemoglobin: Avg. mass of Hb / RBC in picograms (Hyper hypochromic)
Mean cell hemoglobin concentration: Avg. concentration of hemoglobin in a given volume of packed red cells in g/dL
What is the underlying mechanism of blood loss anemia?
Acutely: Trauma
Chronic: GI tract lesions, gynecologic disturbances
What is the underlying mechanism of Intrinsic Hemolytic Anemias?
Heredity
Membrane abnormalities
Membrane skeleton proteins (Spherocytosis, elliptocytosis)
Membrane lipids (abetalipoproteinemia)
Enzyme deficiencies
Enzymes of PPP: G-6-PD, glutathione synthetase
Glycolytic enzymes: pyruvate kinase, hexokinase
Disorders of hemoglobin synthesis
Structurally abnormal globin synthesis (hemoglobinopathies): Sickle Cell Anemia, unstable hemoglobins
Structurally abnormal globin synthesis: Thalassemia Syndromes
Aquired
Membrane defect: Paroxysmal nocturnal hemoglobinuria
What is the underlying mechanism of Extrinsic Hemolytic Anemias?
Antibody-mediated
Isohemagglutinins: Transfusion reactions, Rh disease of the newborn
Autoantibodies: Idiopathic (primary), drug associated, SLE
Mechanical trauma to red cells
Microangiopathic hemolytic anemias: TTP, DIC; Defective cardiac valves
Infections
Malaria
What is the underlying mechanism of Impaired Red Cell Production?
Disturbed proliferation and differentiation of stem cells: Aplastic Anemia
Disturbed proliferation and Maturation of Erythroblasts
Defective DNA synthesis: Vitamin B12 and Folic acid deficiency
Anemia of renal failure (erythropoietin deficiency)
Anemia of chronic disease (iron sequestration, relative EPO deficiency)
Anemia of endocrine disorders
Defective hemoglobin synthesis
Deficient heme synthesis:irin deficiency, sideroblastic anemias
Deficient globin syunthesis: Thalassemias
Marrow replacement: Primary hematopoietic neoplasms
Marrow infiltration: Metastic neoplasms, granulomatous disease