Test 2 - Chapters 5,6,10
Quiz yourself by thinking what should be in
each of the black spaces below before clicking
on it to display the answer.
Help!
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| show | macroovalocytes
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| show | Chemotherapy, Postsplenectomy, and reticulocytosis
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| show | Hypoglycemic patients
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| Ineffective erythropoiesis is defined as: | show 🗑
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| show | Parietal cells of the stomach
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| show | Tropical sprue
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| show | Pernicious anemia
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| show | Pernicious anemia, liver disease, and response to anemic stress
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| show | Thalassemia
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| show | Decreased rate of globin synthesis
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| When platelets concentrate at the edges and feathered end of a blood smear, it is usually due to: | show 🗑
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| show | inadequate mixing of blood and anticoagulant
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| The anemia of chronic infection is characterized by: | show 🗑
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| show | ineffective erythropoiesis
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| show | thalassemia minor
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| What sets of laboratory findings is consistant with hemolytic anemia? | show 🗑
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| show | a quantitative deficiency in RNA resulting in decreased globin chain production
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| Hemoglobin H disease results from: | show 🗑
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| show | serum iron is decreased, transferrin saturation is decreased, TIBC is normal or decreased
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| show | iron overload in tissue
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| show | target cells
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| show | basophilic stippling
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| A 17-year-old boy is admitted to the hospital with a fever of unknown origin. His WBC count is 20.0 x 10^9/L. All of the following can be seen on his peripheral smear: | show 🗑
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| A typical blood picture in infectious mononucleosis is an absolute: | show 🗑
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| A patient who presents with low white cell count, thrombocytopenia, elevated liver enzymes, and mulberry-like inclusions in the granulocytes is most likely suffering from: | show 🗑
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| What statement is common to most lipid storage disease? | show 🗑
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| An autosomal disorder that manifests itself with large lysosomal inclusions, recurring infections, and albinism is: | show 🗑
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| What is an unusual complication that may occur in infectious mononucleosis? | show 🗑
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| show | Neutrophils
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| Toxic granulation in neutrophils is a direct result of: | show 🗑
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| Pelger-Huet anomaly is characterized mainly by: | show 🗑
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| show | Ribosomal RNA
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| show | Alder's anomaly
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| In which white cell disorder will you see gray-green cytoplasmic granules in the neutrophils? | show 🗑
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| show | Gaucher's disease, Tay-Sachs disease, Niemann-Pick disease
NOT: Chediak-Higashi syndrome
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| What shows the three stages of iron defiency anemia in order form first to third? | show 🗑
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| show | chronic infection
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| In anemia of chronic inflammation, which is increased? | show 🗑
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| show | Hemoglobin
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| Lead poisoning is associated with: | show 🗑
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| show | defective genes
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| Iron overload damages all of the following cells: | show 🗑
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| show | phlebotomy
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| show | chelation
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| What can cause a B12 deficiency? | show 🗑
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| Lab finding common for megaloblastic anemia include all of the following: | show 🗑
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| show | Decreased
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| Megaloblastic anemias result in cells that are: | show 🗑
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| show | increased
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| In a megaloblastic anemia, what result would be expected for a bilirubin test? | show 🗑
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| show | Increased
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| A bone marrow aspiration/examination is not necessary for patients with megaloblastic anemia. | show 🗑
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| show | megaloblastic anemia--specifically: pernicious anemia
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Created by:
Megan Hohenberg
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