Hematology 2 Flashcards
Q: which of the following causes microcytic anemia?
- B12 deficiency.
- Aplastic anemia.
- Anemia of renal disease.
- Anemia of Chronic disease.
Anemia of chronic disease
Q: Angular cheilosis and koilonychia are characteristics of which of the following?
- Chronic IDA.
- Aplastic anemia.
- Thalassemia.
- B12 deficiency.
Chronic IDA
Q: Plummer vinson syndrome is associated with?
- SCD.
- Lymphoma.
- Thalassemia.
- Chronic IDA.
Chronic IDA
Q: Prussian blue stain is used to diagnose?
- Thalassemia.
- IDA.
- Sideroblastic anemia.
- Aplastic anemia.
IDA
Q: Which of the following is the most common anemia in hospitalized patients?
- IDA.
- ACD.
- SC anemia.
- Aplastic anemia.
Anemia of chronic disease
Q: which type of anemias is associated with release of hepcidin from the liver?
- ACD.
- IDA.
- SC anemia.
- Aplastic anemia.
Anemia of chronic disease
Q: Which of the following anemias is associated with iron accumulation in the mitochondria?
- IDA.
- ACD.
- Sideroblastic anemia.
- Aplastic anemia.
Sideroblastic anemia
Q: Pyredoxine (B6) deficiency is associated with?
- IDA.
- ACD.
- Sideroblastic anemia.
- Aplastic anemia.
Sideroblastic anemia
Q: Which of the following anemias is most commonly caused by chronic alcoholism?
- IDA.
- ACD.
- Sideroblastic anemia.
- Aplastic anemia.
Sideroblastic anemia ( in 30% of hospitalized ch.alcoholics )
Q: A patient with TB and under Isoniazid. Which of the following anemias can be suspected?
- IDA.
- ACD.
- Sideroblastic anemia.
- Aplastic anemia.
Sideroblastic anemia
Q: course basophilic stippling of RBCs is a clinical feature of?
- B6 deficiency.
- lead poisoning.
- ALA synthase deficiency.
- Ferrochelatse overload.
Lead poisoning (due to denatured ribonuclease) => causing Sideroblastic anemia.
Q: Thalassemia is characterized by?
- Autosomal dominant.
- Autosomal recessive.
- X linked.
- Non of the above.
Autosomal recessive
Q: alpha thalassemia is caused by?
- Gene deletions.
- Point mutation.
- Gene translocation.
- Non of the above.
Gene deletions (4 genes in ch. 16 controls alpha chains)
Q: which of the following will show normal Hb electrophoresis?
- SCA.
- Alpha thalassemia trait.
- Hb H disease.
- Hb Bart disease.
Alpha thalassemia trait
Q: Beta thalassemia is characterized by?
- Gene deletion.
- Point mutation.
- Gene translocation.
- Non of the above.
Point mutation (2 genes in ch. 11 controls B chains)