Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
44 Cards in this Set
- Front
- Back
Microcytic, hypochromic anemia types (MCV < 80)
|
Iron deficiency
alpha-thalassemia beta-thalassemia Lead poisoning Sideroblastic anemia |
|
Iron deficiency anemia
|
Decreased iron due to chronic bleeding
Malnutrition/absorption disorders Increased iron demand (pregnancy) Decreased hemesynthesis |
|
Iron deficiency findings
|
Micocytosis and hypochromia
May manifest as Plummer-vinson syndrome |
|
Alpha-thalassemia
|
Defect alpha-globin gene mutations
Decreased alpha-globin synthesis Prevalent in Asian and African populations |
|
Alpha-thalassemia findings
|
4 gene deletions Hb Barts (gamma 4)
Incompatible with life (cause hydropsfetalis) Three gene deletions HbH disease (beta 4) 1-2 gene deletion: no significant anemia |
|
Beta-thalassemia
|
Point mutations in splice sites + promoter sequences
Decreased beta-globin sythesis Prevalent in Mediterranean populations |
|
Beta-thalassemia minor findings
|
Heterozygote
Beta chain is underproduced Asymptomatic Increased HbA2 (> 3.5%) |
|
Beta-thalassemia major findings
|
Homozygote
Beta chain is absent Requires blood transfusion Marrow expansion -->skeletal deformities (chipmonk f) |
|
Both major and minor beta-thalassemia
|
Increased HbF
|
|
HbS/beta-thalassemia minor
|
Mild to moderate sickle cell disease
|
|
Vitamin B12 deficiency
|
Macrocytic, megaloblastic anemia
Hypersegmented PMNs Neurologica symptoms due to abnormal mylein Prolonged deficiency = nervous system damage |
|
Vitamin B12 found in
|
Animal products
Synthesized by microorganisms |
|
Vitamin B12 stored in
|
Liver for several years
|
|
Vitamin B12 deficiency caused by
|
Sprue
Malabsoprtion (Enteritis + Diphyllobothrium latum) Lack of intrinsic factor (pernicous anemia, gastric bp) Absence of terminal ilieum (Crohn's disease) |
|
Findings of megalobalstic anemia due to B12 deficiency
|
Hypersegmented neutrophils
Glossitis Decreased B12 Increased homocysteine + increased methylmalonic a Neurological symptoms |
|
Deficiency in folic acid
|
Macrocytic, megaloblastic anemia w/o neuro problems
|
|
Causes of folic acid deficiency
|
Alcoholism + pregnancy
Phenytoin, sulfonamides MTX |
|
Findings of megalobalstic anemia due to folate deficiency
|
Hypersegmented neutrophils
Glossitis Decreased folate Increased homocysteine + normal methylmalonic acid |
|
Sideroblastic anemia
|
Defect in heme synthesis
Hereditary X-lined defect in delta-aminolevulinic acid syn |
|
Causes of Sideroblastic anemia
|
Alcohol + lead
|
|
Findings of sideroblastic anemia
|
Ringed sideroblasts (Fe in mito)
Increased iron, normal TIBC, increased ferritin |
|
Treatment of sideroblastic anemia
|
Pyridoxine (B6) therapy
|
|
Macrocytic anemia
|
MCY > 100
Impaired DNA synthesis: (Mat of Nuc delayed = big cell) |
|
Two types of macrocytic anemia
|
Megaloblastic + Nonmegaloblastic
|
|
Megaloblast
|
Large Erythroblast
|
|
Erythroblast
|
Precursor to erythrocyte
Retains nucleus |
|
Nonmegaloblastic macrocytic anemia
|
Macrocytic anemia where DNA synthesis is unimpaired
|
|
Causes of Nonmegaloblastic macrocytic anemia
|
Liver disease, alcoholism
Reticulocytosis --> Inc MCV Metabolic disorder Congenital deficiencies of purine/pyrmidine syn 5-FU, AZT Hydroxyurea |
|
Normocytic, normochromic anemia
|
Classified as nonhemolytic or hemolytic
|
|
Intravascular hemolysis anemia findings
|
Decreased haptoglobin
Increased LDH Hemoglobin in urine (paroxysmal nocturnal) Hemoglobinuria Mechanical destruction (aortic stenosis + prosth valve) |
|
Extravascular hemolysis anemia findings
|
Macrophage in spleen clears RBC
Increased LDH + increased UCB causing jaundice |
|
Types of nonhemolytic, normocytic anemia
|
Anemia of chronic disease
Aplastic anemia Kidney disease |
|
Anemia of chronic disease
|
Inflammation causes increased hepcidin
Causes decreased release of iron from macrophages |
|
Anemia of chronic disease findings
|
Decreased iron
Decreased TIBC Increased ferritin Can become microcytic, hypochromic in long disease |
|
Aplastic anemia
|
Failure/destruction of myleiod stem cells
|
|
Aplastic anemia findings
|
Pancytopenia
Hypocellular bone marrow w/fatty infiltration |
|
Pancytopenia
|
Reduction in red + white blood cells
Reduction in platelets |
|
Symptoms of Aplastic anemia
|
Fatigue
Malaise Pallor Purpura Mucosal bledding Petechiae |
|
Petechiae
|
Red/purple spots on skin
|
|
Treatment of aplastic anemia
|
Windrawal of offending agent
Immunosuppresive regimens Allogenic bone marrow transplant RBC + platelet transfusion G-CSF or GM-CSF |
|
Kidney disease anemia
|
Decreased erythropoietin --> decreased hematopoiesis
|
|
Hereditary spherocytosis (E)
|
Defect in ankrin, band 3, protein 4.2, or spectrin
Causes small, round RBCs No central pallor Increased MCHC + Increased RDW |
|
Findings of hereditary spherocytosis
|
Splenomegaly, aplastic crisis
Hwell-Jolly bodies present after splenectomy |
|
Treatment of hereditary spherocytosis
|
Splenectomy
|