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Hematology 1
Hematology in Practice - Chapter 5
| Question | Answer |
|---|---|
| Transferrin receptors for iron uptake are located on the: | Pronormoblast |
| In addition to iron ingestion, over 90% of iron in adults that is used for erythropoiesis is obtained through: | Recycling of iron |
| All of the following are symptoms of iron deficiency anemia except: A. Pallor B. Pica C. Vertigo D. Numbness | D. Numbness |
| Ringed sideroblasts in the bone marrow are characteristics of which of the following disorders? | Sideroblastic Anemia |
| Which type of inclusion is likely to be seen in the above patient? | Pappenheimer bodies |
| The alpha thalassemic condition that is incompatible with life is: | Bart's hydrops fetalis |
| Failure to thrive, facial structure abnormalities, severe anemia, and splenomegaly are signs of what disorder? | Thalassemia major |
| What laboratory tests would be abnormal through each stage of iron deficiency? | Serum ferritin |
| What is true regarding iron absorption? | Ascorbic acid (vitamin C) enhances absorption |
| Heme is composed of iron and: | protoporphyrin IX |
| Good dietary sources of iron include all except: A. Meat B. Fruit C. Fortified flour D. Legumes | B. Fruit |
| What are the major storage sites for iron in a normal individual? | liver and spleen |
| A markedly decreased iron percent saturation is consistent with: | iron deficiency |
| A bone marrow Prussian blue stain shows blue granules inside of macrophages. What disorder can be ruled out? | Iron deficiency |
| What is true about iron absorption? | It must be in ferrous form for absorption. |
| Lack of accessible iron is the mechanism for iron deficiency and what? | Anemia of chronic inflammation |
| Where is most of the iron in the body found? | Attached to hemoglobin in the red blood cells |
| What results are typical in stage 3 iron deficiency anemia? | Low mean cell volume (MCV), mean cell hemoglobin (MCH), and mean cell hemoglobin concentration (MCHC) |
| What is the mechanism for the anemia in chronic inflammation (ACI)? | Hepcidin, lactoferrin, and ferritin impair iron mobilization |
| How does lead exposure and the porphyrias cause anemia? | interfere with heme production |
| Why is too much iron dangerous? | Free radicals and superoxide formed from ferrous iron plus oxygen damage cell membranes |
| What is true of stage 3 iron deficiency? | Free erythrocyte protoporphyrin (FEP) is increased |
| What would point to iron deficiency anemia (IDA) as opposed to the anemia of chronic inflammation (ACI)? | High transferrin |
| What is the basic hemoglobin defect in the thalassemias? | A structurally normal globin chain is absent or produced at lower levels. |
| What is the primary mechanism for anemia in the thalassemias? | An imbalance in the rate of globin chain synthesis |
| What is expected findings in beta-thalassemia minor? | Basophilic stippling |
| Homozygous alpha-thalassemia (-/-) has what clinical outcome? | incompatible with life |
| In regards to the thalassemias, the deficit has nothing to do with iron. | True |
| The morphologic classification of anemias is based on the: | Red blood cell indices |
| What symptom is specific for IDA? | Koilonychia |
| What laboratory test would be abnormal through each stage of iron deficiency? | Serum ferritin |
| A patient presents with a microcytic, hypochromic anemia with ragged-looking red blood cells in the peripheral smear and a high reticulocyte count. A brilliant cresyl blue preparation reveals inclusions that look like pitted golf balls. What disease? | Hgb H disease |
| The most cost-effective therapy for a patient with hereditary hemochromatosis is: | therapeutic phlebotomy |
| List two sets of laboratory data that can distinguish IDA from beta thalassemia trait: | Serum iron and RBC |
| What is the majority hemoglobin in thalassemia major? | Hgb F |
| Of the four clinical states of alpha thalassemia, which is incompatible with life? | Bart's hydrops fetalis |
| What hemoglobin has the chemical confirmation B4? | Hgb H |
| Although there are many complications in individuals with thalassemia major, what is the leading cause of death? | Cardiac complications |