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WorksheetsRBC & WBC
Total questions: 20
Worksheet time: 20mins
Reed Sternberg cells are found in:
Hodgkin's disease
Thalassemia
Sickle cell carcinoma
CML
Dohle bodies are seen in which of the following?
Multiple Myeloma
May-hegglin anomaly
Waldenstrom Macroglobulinemia
Lymphoma
Malignant hyperplasia of the multipotential myeloid stem cell causes an increase in all cell lines.
Polycythemia Vera
Acute Myeloproliferative Disorders
Hairy B cell Leukemia
Prolymphocytic Leukemia
Laboratory: Bone marrow plasma cells >30%, marked rouleaux, increased erythrocyte sedimentation rate (ESR), the blue background to blood smear, plasma cells and lymphocytes on a blood smear. Presence of Bence Jones proteins in the urine
Polycythemia Vera
Acute Myeloproliferative Disorders
Hairy B cell Leukemia
Multiple Myeloma
What is the term for cell movement through blood vessels to a tissue site?
Diapedesis
Opsonization
Margination
Chemotaxis
Which of the following represents the principal defect in chronic granulomatous disease (CGD)?
Chemotactic migration
Phagocytosis
Lysosomal formation and function
Oxidative respiratory burst
Which of the following are the contents of basophilic granules?
Heparin
Histamine
Myeloperoxidase
Both Heparin and Histamine
The nucleus is a dumbbell or peanut-shaped referred to as “pince-nez”
Pelger-Huet Anomaly
May-Hegglin
Alder-Reilly
Chediak-Higashi
Laboratory: Pancytopenia; cytoplasm of lymphocytes shows hair-like projections; hairy cells are tartrate-resistant acid phosphatase (TRAP) stain positive
Acute Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
Hairy B cell Leukemia
Prolymphocytic Leukemia
Laboratory: Neutropenia, anemia, and thrombocytopenia; variable WBC count; hypercellular marrow with bone marrow blasts >20% (WHO) or >30% (FAB)
Acute Lymphocytic Leukemia
Acute Myeloproliferative Disorders
Hairy B cell Leukemia
Prolymphocytic Leukemia
Transport non-heme iron across the mucosal membrane of the intestines
Transferrin
DMT
IRP-1 & IRP-2
Ferritin
Plummer-Vinson Syndrome includes the following except:
Glossitis
Dysphagia
IDA
none of the above
The only vitamin exclusively synthesized by microorganisms
Folic Acid
Thiamine
Cobalamin
Pyridoxine
Characterized by reduced reticulocyte response accompanied by low serum iron despite adequate iron stores with the presence of high levels of cytokines
Pernicious Anemia
IDA
Anemia of Renal Insufficiency
Anemia of Chronic Disease
Associated with marrow replacement by abnormal cells or tissue component such as metastatic carcinoma, multiple myeloma, leukemia, lipidoses, or storage disease
Porphyria
Myelopthisic Anemia
Aplastic Anemia
Fanconi’s Anemia
Laboratory findings are those of a chronic extravascular hemolytic process: evidence of increased pigment catabolism, erythroid hyperplasia, and reticulocytosis
Hereditary Spherocytosis
Hereditary Stomatocytosis
Hereditary Sickle Cell disease
Paroxysmal Nocturnal Hemoglobinuria
In sickle cell disease, the glutamic acid in the sixth position on the β-chain is replaced by ____________
Phenylalanine
Glutamine
Arginine
Valine
A subgroup of alpha-thalassemia characterized by one defective gene
Hb H disease
Hydrops fetalis
Thalassemia minor
Silent carrier
A 24-year-old woman was rushed to the emergency room due to severe anemia secondary to pneumonia. Genetic studies show her red cells have increased susceptibility to oxidation during intercurrent illness. Peripheral blood shows poikilocytes, some spherocytes, bite cells, and irregularly contracted cells.
Sickle cell disease
G6PD deficiency
Hereditary Pyropoikilocytosis
Hereditary Sideroblastic Anemias
A type of polycythemia wherein the red cell mass is often high normal and the plasma volume is low normal and patients with these type have been regarded as an extreme of the normal physiologic state
Spurious
Absolute
Relative
Intermediate
