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Quiz about Hematology
Quiz about Hematology

Hematology Trivia Quiz


Hematology is the study of blood, where you learn the function of the red blood cells, white blood cells and platelets and the disorders that can occur. This quiz is for hematologists.

A multiple-choice quiz by keijjie. Estimated time: 6 mins.
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Author
keijjie
Time
6 mins
Type
Multiple Choice
Quiz #
400,161
Updated
Dec 03 21
# Qns
10
Difficulty
Tough
Avg Score
5 / 10
Plays
176
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Question 1 of 10
1. Hemoglobin is a protein found in our red blood cells. We must have a certain amount. Which hemoglobin level indicates that the patient requires a transfusion? Hint


Question 2 of 10
2. A peripheral blood smear is a slide made from a drop of a person's blood. This is then stained and observed under the microscope. In megaloblastic anemia, what would you find in the peripheral blood smear? Hint


Question 3 of 10
3. Some conditions are associated with chromosomal abnormalities. These are abnormalities where there are incorrect numbers of chromosomes or an alteration of a chromosome. Which chromosomal abnormality is found in chronic myeloid leukemia (CML)? Hint


Question 4 of 10
4. What is the composition of the protein chains of hemoglobin A1? Hint


Question 5 of 10
5. What globin chain is lacking in beta thalassemias? Hint


Question 6 of 10
6. Brain hemorrhage occurs when platelet levels are below which level? Hint


Question 7 of 10
7. What causes megaloblastic anemia? Hint


Question 8 of 10
8. Lymphocytes are a type of white blood cell. Like all blood cells, they are formed in the bone marrow. Where do lymphocytes mature? Hint


Question 9 of 10
9. Sickle cell anemia is an inherited condition which is autosomal recessive. Due to a mutation in the DNA of the beta globin gene, the beta globin chain has what amino acid change in position 6? Hint


Question 10 of 10
10. Auer rods are seen in which type of leukemia? Hint



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Quiz Answer Key and Fun Facts
1. Hemoglobin is a protein found in our red blood cells. We must have a certain amount. Which hemoglobin level indicates that the patient requires a transfusion?

Answer: 7 g/dL

A level of 7 g/dL means the person has severe anemia and requires a blood transfusion. 16-18 g/dL is the range for a male. At 10 g/dL, the person has mild anemia.
2. A peripheral blood smear is a slide made from a drop of a person's blood. This is then stained and observed under the microscope. In megaloblastic anemia, what would you find in the peripheral blood smear?

Answer: hypersegmented neutrophils and macroovalocytes

Larger red blood cells (macroovalocytes) and hypersegmented neutrophils are characteristic of megaloblastic anemia. Microcytes are typical of iron deficiency anemia. Hypolobulated neutrophils (e.g., Pinz-nez) are often seen in inherited conditions.
3. Some conditions are associated with chromosomal abnormalities. These are abnormalities where there are incorrect numbers of chromosomes or an alteration of a chromosome. Which chromosomal abnormality is found in chronic myeloid leukemia (CML)?

Answer: Philadelphia chromosome

The Philadelphia chromosome results from a balanced translocation between chromosomes 9 and 21. The altered chromosome 21 with the bcr-abl fusion gene is strongly associated with CML. The other conditions are due to extra chromosomes and are not related to CML.
4. What is the composition of the protein chains of hemoglobin A1?

Answer: alpha 2, beta 2

Each hemoglobin consists of four globin chains. The most common adult hemoglobin, Hgb A1 consists of 2 alpha and 2 beta chains. Alpha2 delta 2 is the composition of Hgb A2; alpha2 gamma 2 makes up fetal hemoglobin; beta 4 is the composition of an abnormal hemoglobin in alpha thalassemias.
5. What globin chain is lacking in beta thalassemias?

Answer: beta chain

In thalassemias, one of the adult hemoglobin chains is not produced or produced in lesser amounts. In beta thalassemias, the beta chain is not made. As a result, Hb A1 (alpha 2 beta 2), the major adult hemoglobin is not made. This leads to major organ damage, growth retardation and anemia. The zeta chain is only made in embryonic life.
6. Brain hemorrhage occurs when platelet levels are below which level?

Answer: 30,000/microliter

Platelets or thromobocytes are tiny "cells" which initiate the blood clotting process in response to cuts or tissue trauma. The normal level of platelets is 150-400,000 per microliter. With lower levels of platelets petechiae or hemorrhages under the skin are seen. Very low platelet levels cause spontaneous internal hemorrhages including fatal brain hemorrhages.
7. What causes megaloblastic anemia?

Answer: Vitamin B12 deficiency

Vitamin B12 and/or folate deficiency causes megaloblastic anemia. This results from the precursor cells not being able to make DNA properly. The red cell precursors will have nuclear-cytoplasmic asynchronu=y where the cytoplasm matures faster than the nucleus.

The resulting cells are larger than normal (megaloblastic). Iron (Fe) deficiency causes a microcytic anemia where the red blood cells are too small. Vitamin C deficiency causes scurvy while vitamin A deficiency causes skin problems and night blindness.
8. Lymphocytes are a type of white blood cell. Like all blood cells, they are formed in the bone marrow. Where do lymphocytes mature?

Answer: Bone marrow and thymus

The bone marrow is where B lymphocytes mature and the thymus is where T lymphocytes mature. The spleen is a secondary lymphoid organ and is an organ where blood cells are stored. The liver is an important organ with many functions but lymphocytes do not mature here.
9. Sickle cell anemia is an inherited condition which is autosomal recessive. Due to a mutation in the DNA of the beta globin gene, the beta globin chain has what amino acid change in position 6?

Answer: glutamic acid to valine

The change of a polar amino acid (glutamic acid) to a non-polar amino acid (valine) exposes a hydrophobic pocket in the hemoglobin protein. Because of this, the Hemoglobin molecules form long fibers and distort the red blood cell shape under low Oxygen concentrations.

A person must inherit 2 of the defective alleles from each parent to have sickle cell anemia. The DNA of a gene is transcribed to mRNA which is then translated to a protein. In this case, the defect in the gene is manifested by an abnormal protein.
10. Auer rods are seen in which type of leukemia?

Answer: Acute myeloid leukemia

Auer rods are formed from the nonspecific granules in the cytoplasm of myeloid precursors (the white blood cells that are not lymphoid) fusing together. They are highly specific for myeloid leukemias. Megakaryocytic leukemia is from neoplasia of a megakaryoblast (a platelet precursor).
Source: Author keijjie

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