Podcast
Questions and Answers
What is assessed by running a sample multiple times?
What is assessed by running a sample multiple times?
What effect would a buffer of pH 6.0 have on a Wright-stained smear?
What effect would a buffer of pH 6.0 have on a Wright-stained smear?
What disease is Howell-Jolly body associated with?
What disease is Howell-Jolly body associated with?
At what age is a lymphocyte count of 60% considered normal?
At what age is a lymphocyte count of 60% considered normal?
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What is Drabkin's reagent used for measuring?
What is Drabkin's reagent used for measuring?
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What is the corrected WBC count if the total count is 20 x 10^9/L and the percentage of nucleated RBC is 25?
What is the corrected WBC count if the total count is 20 x 10^9/L and the percentage of nucleated RBC is 25?
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What type of inclusions are seen in cases of burn?
What type of inclusions are seen in cases of burn?
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What is characterized by the presence of lavender granules and multiple granules in lymphocytes and neutrophils?
What is characterized by the presence of lavender granules and multiple granules in lymphocytes and neutrophils?
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What is the range of red cell count in males?
What is the range of red cell count in males?
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Which of the following factors is activated by activated factor 2?
Which of the following factors is activated by activated factor 2?
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What is the antidote for an overdose of coumadin?
What is the antidote for an overdose of coumadin?
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What is the result that yields abnormal in DIC but usually within the reference interval or just slightly abnormal in TTP and HUS?
What is the result that yields abnormal in DIC but usually within the reference interval or just slightly abnormal in TTP and HUS?
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What is the factor deficiency when APTT and PT are corrected by adsorbed plasma?
What is the factor deficiency when APTT and PT are corrected by adsorbed plasma?
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What is the first factor affected by warfarin?
What is the first factor affected by warfarin?
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What is the responsible for platelet shape change during activation?
What is the responsible for platelet shape change during activation?
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What is the association with DIC?
What is the association with DIC?
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What is the anticoagulant to blood ratio in coagulant studies?
What is the anticoagulant to blood ratio in coagulant studies?
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What is the best test for monitoring oral anticoagulant therapy?
What is the best test for monitoring oral anticoagulant therapy?
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What is the cause of gum bleeding, deep bruising, and nose bleeding?
What is the cause of gum bleeding, deep bruising, and nose bleeding?
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What is the deficiency that causes thrombosis due to a lack of fibrinolysis?
What is the deficiency that causes thrombosis due to a lack of fibrinolysis?
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What is the sample used for prothrombin time?
What is the sample used for prothrombin time?
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What is the number of platelets generated by an average megakaryocyte?
What is the number of platelets generated by an average megakaryocyte?
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What is the first stage capable of endomitosis?
What is the first stage capable of endomitosis?
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What is the test used to assess platelet adhesion in vivo?
What is the test used to assess platelet adhesion in vivo?
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What is the consequence of "giant platelet" and "platelet clumping" on the platelet count?
What is the consequence of "giant platelet" and "platelet clumping" on the platelet count?
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Which of the following is the most severe bleeding disorder?
Which of the following is the most severe bleeding disorder?
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What is the preferable site for bone marrow biopsy in children?
What is the preferable site for bone marrow biopsy in children?
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What does hemolysis indicate in the Donath-Landsteiner test?
What does hemolysis indicate in the Donath-Landsteiner test?
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Which CBC parameter reflects the RBC size?
Which CBC parameter reflects the RBC size?
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What is associated with an increased reticulocyte count?
What is associated with an increased reticulocyte count?
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Where does hemoglobin production begin in RBC development?
Where does hemoglobin production begin in RBC development?
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What is calcium known as in coagulation?
What is calcium known as in coagulation?
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Which of the following cells is characterized by having two or more nuclei in plasma cells?
Which of the following cells is characterized by having two or more nuclei in plasma cells?
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What stimulates the release of Erythropoietin in response to decreased renal oxygen tension?
What stimulates the release of Erythropoietin in response to decreased renal oxygen tension?
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Which type of leukemia is characterized by hypergranular or acute promyelocytic leukemia?
Which type of leukemia is characterized by hypergranular or acute promyelocytic leukemia?
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What is the cause of hemolysis in a blood sample?
What is the cause of hemolysis in a blood sample?
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Which cell is indicative of infectious mononucleosis?
Which cell is indicative of infectious mononucleosis?
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What is a characteristic of hypersplenism?
What is a characteristic of hypersplenism?
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What condition can cause an elevated Erythrocyte Sedimentation Rate (ESR)?
What condition can cause an elevated Erythrocyte Sedimentation Rate (ESR)?
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What is the characteristic of Pelger-Huet anomaly?
What is the characteristic of Pelger-Huet anomaly?
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What type of anomaly is characterized by lymphocytes and granulocytes?
What type of anomaly is characterized by lymphocytes and granulocytes?
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What triggers the release of Erythropoietin in response to decreased renal oxygen tension?
What triggers the release of Erythropoietin in response to decreased renal oxygen tension?
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What is the FAB classification of Acute Myeloblastic Leukemia with minimal differentiation?
What is the FAB classification of Acute Myeloblastic Leukemia with minimal differentiation?
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What is the consequence of hemolysis in a blood sample?
What is the consequence of hemolysis in a blood sample?
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What is the characteristic of Hypersplenism?
What is the characteristic of Hypersplenism?
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Which condition is characterized by a high ESR?
Which condition is characterized by a high ESR?
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What is the function of Transcobalamin II?
What is the function of Transcobalamin II?
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What is the characteristic of Pelger-Huet anomaly?
What is the characteristic of Pelger-Huet anomaly?
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What is the consequence of a Wright-stained smear with a buffer of pH 6.0?
What is the consequence of a Wright-stained smear with a buffer of pH 6.0?
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What is the association of Howell-Jolly bodies with disease?
What is the association of Howell-Jolly bodies with disease?
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At what age is a lymphocyte count of 60% considered normal?
At what age is a lymphocyte count of 60% considered normal?
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What is the formula for corrected WBC count?
What is the formula for corrected WBC count?
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What is Drabkin's reagent used for measuring?
What is Drabkin's reagent used for measuring?
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What type of inclusions are seen in cases of burn?
What type of inclusions are seen in cases of burn?
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What is characteristic of Chediak-Higashi anomaly?
What is characteristic of Chediak-Higashi anomaly?
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What is the effect of a buffer of pH 6.0 on a Wright-stained smear?
What is the effect of a buffer of pH 6.0 on a Wright-stained smear?
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What is the range of red cell count in males?
What is the range of red cell count in males?
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In extramedullary hematopoiesis, which organs revert to producing immature blood cells?
In extramedullary hematopoiesis, which organs revert to producing immature blood cells?
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What is the cause of pernicious anemia?
What is the cause of pernicious anemia?
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What is the antidote for an overdose of coumadin?
What is the antidote for an overdose of coumadin?
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Which factor is activated by activated factor 2?
Which factor is activated by activated factor 2?
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What is the result that yields abnormal in DIC but usually within the reference interval or just slightly abnormal in TTP and HUS?
What is the result that yields abnormal in DIC but usually within the reference interval or just slightly abnormal in TTP and HUS?
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What is the factor deficiency when APTT and PT are corrected by adsorbed plasma?
What is the factor deficiency when APTT and PT are corrected by adsorbed plasma?
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What is the first factor affected by warfarin?
What is the first factor affected by warfarin?
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What is the correct sequence of the intrinsic pathway?
What is the correct sequence of the intrinsic pathway?
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What is the correct anticoagulant to blood ratio in coagulant studies?
What is the correct anticoagulant to blood ratio in coagulant studies?
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Which test is used to assess platelet adhesion in vivo?
Which test is used to assess platelet adhesion in vivo?
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What is the consequence of a deficiency in the fibrinolytic system?
What is the consequence of a deficiency in the fibrinolytic system?
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Which of the following is a characteristic of dysfibrinogenemia?
Which of the following is a characteristic of dysfibrinogenemia?
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What is the number of platelets generated by an average megakaryocyte?
What is the number of platelets generated by an average megakaryocyte?
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What is the first stage capable of endomitosis?
What is the first stage capable of endomitosis?
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What is the result of a deficiency in vitamin K?
What is the result of a deficiency in vitamin K?
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What is the effect of platelet satellitism on the platelet count?
What is the effect of platelet satellitism on the platelet count?
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What is the most severe bleeding disorder?
What is the most severe bleeding disorder?
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Where does hemoglobin production begin in RBC development?
Where does hemoglobin production begin in RBC development?
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What is the preferable site for bone marrow biopsy in children?
What is the preferable site for bone marrow biopsy in children?
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What is indicated by hemolysis in the Donath-Landsteiner test?
What is indicated by hemolysis in the Donath-Landsteiner test?
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What is the CBC parameter that reflects the RBC size?
What is the CBC parameter that reflects the RBC size?
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What is the result of an underfilled ProTime vacutainer?
What is the result of an underfilled ProTime vacutainer?
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What is the site of thrombopoietin production in response to platelet demand?
What is the site of thrombopoietin production in response to platelet demand?
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What is the effect of a Wright-stained smear with a buffer of pH 7.4?
What is the effect of a Wright-stained smear with a buffer of pH 7.4?
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What is the significance of a Howell-Jolly body in a patient's blood smear?
What is the significance of a Howell-Jolly body in a patient's blood smear?
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What is the corrected WBC count if the total count is 20 x 10^9/L and the percentage of nucleated RBC is 30?
What is the corrected WBC count if the total count is 20 x 10^9/L and the percentage of nucleated RBC is 30?
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What type of inclusions are seen in cases of burn?
What type of inclusions are seen in cases of burn?
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What is the age group in which a lymphocyte count of 60% is considered normal?
What is the age group in which a lymphocyte count of 60% is considered normal?
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What is Drabkin's reagent used for measuring?
What is Drabkin's reagent used for measuring?
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What is characteristic of Chediak-Higashi anomaly?
What is characteristic of Chediak-Higashi anomaly?
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What is the formula to correct the WBC count for nucleated RBCs?
What is the formula to correct the WBC count for nucleated RBCs?
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What is the characteristic of Russel bodies in plasma cells?
What is the characteristic of Russel bodies in plasma cells?
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What is the consequence of a deficiency in the fibrinolytic system?
What is the consequence of a deficiency in the fibrinolytic system?
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What is the consequence of decreased renal oxygen tension on Erythropoietin production?
What is the consequence of decreased renal oxygen tension on Erythropoietin production?
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What is the best test for monitoring oral anticoagulant therapy?
What is the best test for monitoring oral anticoagulant therapy?
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What is the FAB classification of Acute Myeloblastic Leukemia with maturation?
What is the FAB classification of Acute Myeloblastic Leukemia with maturation?
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What is the characteristic of Chediak-Higashi anomaly?
What is the characteristic of Chediak-Higashi anomaly?
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What is the anticoagulant to blood ratio in coagulant studies?
What is the anticoagulant to blood ratio in coagulant studies?
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What is the sample used for prothrombin time?
What is the sample used for prothrombin time?
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What is the cause of hemolysis in a blood sample?
What is the cause of hemolysis in a blood sample?
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What is the number of platelets generated by an average megakaryocyte?
What is the number of platelets generated by an average megakaryocyte?
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What is the characteristic of hyposegmentation in Pelger-Huet anomaly?
What is the characteristic of hyposegmentation in Pelger-Huet anomaly?
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What is the first stage capable of endomitosis?
What is the first stage capable of endomitosis?
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What is the function of Transcobalamin II?
What is the function of Transcobalamin II?
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What is the characteristic of hypersplenism?
What is the characteristic of hypersplenism?
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What is the test used to assess platelet adhesion in vivo?
What is the test used to assess platelet adhesion in vivo?
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Which of the following would show an abnormal result in fibrinogen deficiency?
Which of the following would show an abnormal result in fibrinogen deficiency?
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What is the site of extramedullary hematopoiesis in emergencies?
What is the site of extramedullary hematopoiesis in emergencies?
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What is the normal range of red cell count in females?
What is the normal range of red cell count in females?
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What is the cause of pernicious anemia?
What is the cause of pernicious anemia?
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What is the highest muramidase activity found in?
What is the highest muramidase activity found in?
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Which of the following results yields abnormal in DIC but usually within the reference interval or just slightly abnormal in TTP and HUS?
Which of the following results yields abnormal in DIC but usually within the reference interval or just slightly abnormal in TTP and HUS?
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What is the factor deficiency when APTT and PT are corrected by adsorbed plasma?
What is the factor deficiency when APTT and PT are corrected by adsorbed plasma?
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What is the first factor affected by warfarin?
What is the first factor affected by warfarin?
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What is the association with DIC?
What is the association with DIC?
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What is the consequence of 'giant platelet' and 'platelet clumping' on the platelet count?
What is the consequence of 'giant platelet' and 'platelet clumping' on the platelet count?
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Which of the following is the most severe bleeding disorder?
Which of the following is the most severe bleeding disorder?
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What is the preferable site for bone marrow biopsy in children?
What is the preferable site for bone marrow biopsy in children?
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What does hemolysis indicate in the Donath-Landsteiner test?
What does hemolysis indicate in the Donath-Landsteiner test?
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Which CBC parameter reflects the RBC size?
Which CBC parameter reflects the RBC size?
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What is associated with an increased reticulocyte count?
What is associated with an increased reticulocyte count?
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Where does hemoglobin production begin in RBC development?
Where does hemoglobin production begin in RBC development?
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What is calcium known as in coagulation?
What is calcium known as in coagulation?
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Study Notes
Hematology
- A sample is run multiple times to assess:
- Precision
- Wright's stain requires a pH of 6.8; a pH of 6.0 would make red cells stain too pink.
- Howell-Jolly bodies are associated with Megaloblastic Anemia.
- Lymphocyte count of 60% is considered normal in children from 6 months to 2 years old.
- Drabkin's reagent is used to measure Cyanmethemoglobin.
- Corrected WBC count = [100/(100+nRBC)] x WBC count.
- Dohle bodies are seen in cases of burn.
- Chediak-Higashi anomaly is characterized by lavender granules and multiple granules present in lymphocytes and neutrophils.
- Erythropoietin production can be increased due to decreased renal oxygen tension.
- FAB classification of Acute Myeloblastic Leukemia includes:
- M1 and M2
- Hemolysis can be caused by transfusing blood too fast into a tube.
- Reactive lymphocytes are indicative of infectious mononucleosis.
- Hypersplenism is characterized by Leukopenia and Thrombocytopenia.
- An elevated ESR can be caused by Inflammation.
- Spherocytes are detected in Autoimmune Hemolytic Anemia (AIHA).
- Transcobalamin II is responsible for transporting cobalamin from the bloodstream to cells throughout the body.
- Pelger-Huet anomaly is characterized by a dumbbell-shaped nucleus in neutrophils.
- All of the following are reliable criteria for differentiating mature from immature cells:
- Nucleus
- Cytoplasm
- Nuclear Chromatin
- Extramedullary hemostasis does not occur in the bone marrow.
Coagulation
- The preferred blood collection for patients with 5 nRBCs present per 100 WBCs.
- Muramidase (lysosome) activity is highest in M4.
- Extramedullary hematopoiesis in emergencies occurs in the liver.
- Pernicious anemia is caused by a lack of intrinsic factor from the stomach.
- PT and APTT are corrected by adsorbed plasma.
- Factor V deficiency is corrected by adsorbed plasma.
- Vitamin K is the antidote for an overdose of Coumadin.
- Fibrinogen group is activated by activated factor 2.
- APTT and PT are corrected by adsorbed plasma, which suggests a factor deficiency.
- Vitamin K-dependent factors include:
- Fibrinogen
- Prothrombin
- The first factor affected by warfarin is Factor VII.
- Precision in bleeding time is controlled by a standardized wound.
- DIC is associated with:
- Decreased plt count
- Increase in factors I, V, VIII
- Positive D-dimer
- Prolonged APTT
- ADAM-TS 13 is associated with Thrombotic Thrombocytopenic Purpura (TTP).
- Microfilaments are responsible for platelet shape change during activation.
- Vitamin K-dependent factors include:
- Fibrinogen
- Prothrombin
- The anticoagulant to blood ratio in 3.2% sodium citrate in coagulant studies is 1:9.
- The Cascade theory involves the intrinsic pathway:
- Factor 12 -> 11 -> 9 -> 8 -> 10
- PT is used to monitor oral anticoagulant therapy.
- Deficiency of the fibrinolytic system causes Thrombosis.
Platelet and Blood Cells
- Gum bleeding, deep bruising, and nose bleeding are symptoms of Platelet defect.
- Multiple factor deficiency is associated with Severe liver disease.
- Dysfibrinogenemia is a qualitative fibrinogen deficiency.
- An average megakaryocyte generates approximately 2000 platelets.
- The first stage capable of endomitosis is the LD-CFU-Meg.
- Bleeding time assesses platelet adhesion in vivo.
- Fibrinogen deficiency would show abnormal results in:
- Thrombin Time
- Prothrombin Time
- Platelet aggregation tests
- The late stage of megakaryoblast marks the beginning of alpha granules formation.
- The entire central large square is used for counting platelets in a hemocytometer.
- A biphasic curve is shown by:
- a&c (adrenaline and collagen)
- PFA-100 is used to assess qualitative platelet defects.
- Spurious decreased platelet count can be caused by:
- Giant platelet
- Platelet clumping
- Platelet satellitism
- Red cell inclusion
- Hemophilia B is the most severe bleeding disorder.
- The preferable site for bone marrow biopsy in children is the posterior iliac crest.
RBC and Hemoglobin
- Hemolysis in the Donath-Landsteiner test is positive for Donath-Landsteiner antibody.
- RBC size is reflected in the MCV parameter.
- Increased reticulocyte count is reflected in Polychromasia.
- Basophilic normoblast is the stage where Hb maturation starts.
- Calcium is not considered a coagulation factor but is known as Factor IV.
Hematology
- A sample is run multiple times to assess:
- Precision
- Wright's stain requires a pH of 6.8; a pH of 6.0 would make red cells stain too pink.
- Howell-Jolly bodies are associated with Megaloblastic Anemia.
- Lymphocyte count of 60% is considered normal in children from 6 months to 2 years old.
- Drabkin's reagent is used to measure Cyanmethemoglobin.
- Corrected WBC count = [100/(100+nRBC)] x WBC count.
- Dohle bodies are seen in cases of burn.
- Chediak-Higashi anomaly is characterized by lavender granules and multiple granules present in lymphocytes and neutrophils.
- Erythropoietin production can be increased due to decreased renal oxygen tension.
- FAB classification of Acute Myeloblastic Leukemia includes:
- M1 and M2
- Hemolysis can be caused by transfusing blood too fast into a tube.
- Reactive lymphocytes are indicative of infectious mononucleosis.
- Hypersplenism is characterized by Leukopenia and Thrombocytopenia.
- An elevated ESR can be caused by Inflammation.
- Spherocytes are detected in Autoimmune Hemolytic Anemia (AIHA).
- Transcobalamin II is responsible for transporting cobalamin from the bloodstream to cells throughout the body.
- Pelger-Huet anomaly is characterized by a dumbbell-shaped nucleus in neutrophils.
- All of the following are reliable criteria for differentiating mature from immature cells:
- Nucleus
- Cytoplasm
- Nuclear Chromatin
- Extramedullary hemostasis does not occur in the bone marrow.
Coagulation
- The preferred blood collection for patients with 5 nRBCs present per 100 WBCs.
- Muramidase (lysosome) activity is highest in M4.
- Extramedullary hematopoiesis in emergencies occurs in the liver.
- Pernicious anemia is caused by a lack of intrinsic factor from the stomach.
- PT and APTT are corrected by adsorbed plasma.
- Factor V deficiency is corrected by adsorbed plasma.
- Vitamin K is the antidote for an overdose of Coumadin.
- Fibrinogen group is activated by activated factor 2.
- APTT and PT are corrected by adsorbed plasma, which suggests a factor deficiency.
- Vitamin K-dependent factors include:
- Fibrinogen
- Prothrombin
- The first factor affected by warfarin is Factor VII.
- Precision in bleeding time is controlled by a standardized wound.
- DIC is associated with:
- Decreased plt count
- Increase in factors I, V, VIII
- Positive D-dimer
- Prolonged APTT
- ADAM-TS 13 is associated with Thrombotic Thrombocytopenic Purpura (TTP).
- Microfilaments are responsible for platelet shape change during activation.
- Vitamin K-dependent factors include:
- Fibrinogen
- Prothrombin
- The anticoagulant to blood ratio in 3.2% sodium citrate in coagulant studies is 1:9.
- The Cascade theory involves the intrinsic pathway:
- Factor 12 -> 11 -> 9 -> 8 -> 10
- PT is used to monitor oral anticoagulant therapy.
- Deficiency of the fibrinolytic system causes Thrombosis.
Platelet and Blood Cells
- Gum bleeding, deep bruising, and nose bleeding are symptoms of Platelet defect.
- Multiple factor deficiency is associated with Severe liver disease.
- Dysfibrinogenemia is a qualitative fibrinogen deficiency.
- An average megakaryocyte generates approximately 2000 platelets.
- The first stage capable of endomitosis is the LD-CFU-Meg.
- Bleeding time assesses platelet adhesion in vivo.
- Fibrinogen deficiency would show abnormal results in:
- Thrombin Time
- Prothrombin Time
- Platelet aggregation tests
- The late stage of megakaryoblast marks the beginning of alpha granules formation.
- The entire central large square is used for counting platelets in a hemocytometer.
- A biphasic curve is shown by:
- a&c (adrenaline and collagen)
- PFA-100 is used to assess qualitative platelet defects.
- Spurious decreased platelet count can be caused by:
- Giant platelet
- Platelet clumping
- Platelet satellitism
- Red cell inclusion
- Hemophilia B is the most severe bleeding disorder.
- The preferable site for bone marrow biopsy in children is the posterior iliac crest.
RBC and Hemoglobin
- Hemolysis in the Donath-Landsteiner test is positive for Donath-Landsteiner antibody.
- RBC size is reflected in the MCV parameter.
- Increased reticulocyte count is reflected in Polychromasia.
- Basophilic normoblast is the stage where Hb maturation starts.
- Calcium is not considered a coagulation factor but is known as Factor IV.
Hematology
- A sample is run multiple times to assess:
- Precision
- Wright's stain requires a pH of 6.8; a pH of 6.0 would make red cells stain too pink.
- Howell-Jolly bodies are associated with Megaloblastic Anemia.
- Lymphocyte count of 60% is considered normal in children from 6 months to 2 years old.
- Drabkin's reagent is used to measure Cyanmethemoglobin.
- Corrected WBC count = [100/(100+nRBC)] x WBC count.
- Dohle bodies are seen in cases of burn.
- Chediak-Higashi anomaly is characterized by lavender granules and multiple granules present in lymphocytes and neutrophils.
- Erythropoietin production can be increased due to decreased renal oxygen tension.
- FAB classification of Acute Myeloblastic Leukemia includes:
- M1 and M2
- Hemolysis can be caused by transfusing blood too fast into a tube.
- Reactive lymphocytes are indicative of infectious mononucleosis.
- Hypersplenism is characterized by Leukopenia and Thrombocytopenia.
- An elevated ESR can be caused by Inflammation.
- Spherocytes are detected in Autoimmune Hemolytic Anemia (AIHA).
- Transcobalamin II is responsible for transporting cobalamin from the bloodstream to cells throughout the body.
- Pelger-Huet anomaly is characterized by a dumbbell-shaped nucleus in neutrophils.
- All of the following are reliable criteria for differentiating mature from immature cells:
- Nucleus
- Cytoplasm
- Nuclear Chromatin
- Extramedullary hemostasis does not occur in the bone marrow.
Coagulation
- The preferred blood collection for patients with 5 nRBCs present per 100 WBCs.
- Muramidase (lysosome) activity is highest in M4.
- Extramedullary hematopoiesis in emergencies occurs in the liver.
- Pernicious anemia is caused by a lack of intrinsic factor from the stomach.
- PT and APTT are corrected by adsorbed plasma.
- Factor V deficiency is corrected by adsorbed plasma.
- Vitamin K is the antidote for an overdose of Coumadin.
- Fibrinogen group is activated by activated factor 2.
- APTT and PT are corrected by adsorbed plasma, which suggests a factor deficiency.
- Vitamin K-dependent factors include:
- Fibrinogen
- Prothrombin
- The first factor affected by warfarin is Factor VII.
- Precision in bleeding time is controlled by a standardized wound.
- DIC is associated with:
- Decreased plt count
- Increase in factors I, V, VIII
- Positive D-dimer
- Prolonged APTT
- ADAM-TS 13 is associated with Thrombotic Thrombocytopenic Purpura (TTP).
- Microfilaments are responsible for platelet shape change during activation.
- Vitamin K-dependent factors include:
- Fibrinogen
- Prothrombin
- The anticoagulant to blood ratio in 3.2% sodium citrate in coagulant studies is 1:9.
- The Cascade theory involves the intrinsic pathway:
- Factor 12 -> 11 -> 9 -> 8 -> 10
- PT is used to monitor oral anticoagulant therapy.
- Deficiency of the fibrinolytic system causes Thrombosis.
Platelet and Blood Cells
- Gum bleeding, deep bruising, and nose bleeding are symptoms of Platelet defect.
- Multiple factor deficiency is associated with Severe liver disease.
- Dysfibrinogenemia is a qualitative fibrinogen deficiency.
- An average megakaryocyte generates approximately 2000 platelets.
- The first stage capable of endomitosis is the LD-CFU-Meg.
- Bleeding time assesses platelet adhesion in vivo.
- Fibrinogen deficiency would show abnormal results in:
- Thrombin Time
- Prothrombin Time
- Platelet aggregation tests
- The late stage of megakaryoblast marks the beginning of alpha granules formation.
- The entire central large square is used for counting platelets in a hemocytometer.
- A biphasic curve is shown by:
- a&c (adrenaline and collagen)
- PFA-100 is used to assess qualitative platelet defects.
- Spurious decreased platelet count can be caused by:
- Giant platelet
- Platelet clumping
- Platelet satellitism
- Red cell inclusion
- Hemophilia B is the most severe bleeding disorder.
- The preferable site for bone marrow biopsy in children is the posterior iliac crest.
RBC and Hemoglobin
- Hemolysis in the Donath-Landsteiner test is positive for Donath-Landsteiner antibody.
- RBC size is reflected in the MCV parameter.
- Increased reticulocyte count is reflected in Polychromasia.
- Basophilic normoblast is the stage where Hb maturation starts.
- Calcium is not considered a coagulation factor but is known as Factor IV.
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Description
A quiz on hematology laboratory techniques and concepts, covering topics such as precision, accuracy, and Wright stained smears.