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Questions and Answers
What is the primary function of platelet activation?
What is the primary function of platelet activation?
- To increase vascular permeability
- To enhance white blood cell activity
- To form a clot at the site of injury (correct)
- To promote blood flow
Which of the following is involved in the eicosanoid synthesis pathway?
Which of the following is involved in the eicosanoid synthesis pathway?
- Adenosine triphosphate (ATP)
- Platelet-activating factor
- G proteins (correct)
- Inositol triphosphate
What factor is linked to the acute coagulopathy of trauma-shock?
What factor is linked to the acute coagulopathy of trauma-shock?
- Hypercoagulability of blood
- Concentration of platelet components
- Increased plasma viscosity
- Decreased platelet aggregation (correct)
Which type of leukemia is characterized by a rapid increase in immature blood cells?
Which type of leukemia is characterized by a rapid increase in immature blood cells?
What is the significance of flow cytometric analysis in acute myeloid leukemia?
What is the significance of flow cytometric analysis in acute myeloid leukemia?
What is the role of G proteins in platelet function?
What is the role of G proteins in platelet function?
Which staining method is commonly utilized to differentiate acute myeloid leukemia cells?
Which staining method is commonly utilized to differentiate acute myeloid leukemia cells?
What is one of the complications of acute hemolytic transfusion reactions?
What is one of the complications of acute hemolytic transfusion reactions?
Which type of leukemia is defined by the presence of abnormal myeloblasts?
Which type of leukemia is defined by the presence of abnormal myeloblasts?
What is the primary treatment goal for managing acute coagulopathy of trauma-shock?
What is the primary treatment goal for managing acute coagulopathy of trauma-shock?
What is the primary function of an aggregometer in hematology?
What is the primary function of an aggregometer in hematology?
What condition is associated with chronic alcohol consumption and its effects on blood?
What condition is associated with chronic alcohol consumption and its effects on blood?
Which laboratory finding is commonly associated with aplastic anemia?
Which laboratory finding is commonly associated with aplastic anemia?
What pathophysiological mechanism underlies a-thalassemia?
What pathophysiological mechanism underlies a-thalassemia?
Which term describes the risk assessment and management strategies to address alloimmunization in blood transfusions?
Which term describes the risk assessment and management strategies to address alloimmunization in blood transfusions?
Which condition is characterized by high levels of circulating immune complexes in the bloodstream?
Which condition is characterized by high levels of circulating immune complexes in the bloodstream?
What type of anemia is characterized by ineffective erythropoiesis and often seen in elderly patients?
What type of anemia is characterized by ineffective erythropoiesis and often seen in elderly patients?
Which diagnostic test is particularly useful for evaluating sickle cell disease?
Which diagnostic test is particularly useful for evaluating sickle cell disease?
Which of the following is a clinical manifestation of allergic purpura?
Which of the following is a clinical manifestation of allergic purpura?
What is the effect of a-granule deficiency on platelet function?
What is the effect of a-granule deficiency on platelet function?
Flashcards
Anemia
Anemia
A decrease in either the number or volume of red blood cells, resulting in reduced oxygen-carrying capacity.
Aplastic anemia
Aplastic anemia
A type of anemia characterized by a deficiency in the production of red blood cells due to a failure of the bone marrow to produce adequate hematopoietic stem cells.
Morphologic classification of Anemia
Morphologic classification of Anemia
A classification of anemia based on the size and color of red blood cells, which provides valuable clues about the underlying cause.
Anemia of chronic inflammation
Anemia of chronic inflammation
Anemia that develops due to an underlying inflammatory process, which inhibits erythropoiesis (red blood cell production).
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Anemia of chronic kidney disease
Anemia of chronic kidney disease
A specific type of anemia that develops in individuals with chronic kidney disease due to impaired production of erythropoietin.
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Congenital dyserythropoietic anemia
Congenital dyserythropoietic anemia
A rare genetic disorder that affects red blood cell production, leading to a deficiency in certain enzymes involved in red blood cell formation.
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Diamond-Blackfan anemia
Diamond-Blackfan anemia
A form of anemia characterized by an underproduction of red blood cells due to the failure of the bone marrow to produce enough red blood cell precursors.
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Fanconi anemia
Fanconi anemia
A rare genetic disorder that affects the development of bone marrow cells, leading to various abnormalities, including anemia.
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Geriatric Anemia
Geriatric Anemia
A common, but often overlooked, health issue in elderly individuals, where the underlying cause may be different than in younger patients.
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Alkaline hemoglobin electrophoresis
Alkaline hemoglobin electrophoresis
A method used to separate different types of hemoglobin based on their electric charge, helping to diagnose various hemoglobinopathies.
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Platelet Adhesion
Platelet Adhesion
The process by which platelets attach to damaged blood vessels, forming a temporary plug to stop bleeding. This is a crucial step in the initial stages of clot formation.
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Platelet Aggregation
Platelet Aggregation
When platelets clump together, forming a larger mass that seals off the damaged area. This is a key part of the process of forming a blood clot.
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Platelet Secretion
Platelet Secretion
The release of chemicals from platelets, such as ADP and thromboxane A2, which further boost the process of clotting. These chemicals alert more platelets to join the party, making the clot even stronger.
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Immune Thrombocytopenia (ITP)
Immune Thrombocytopenia (ITP)
A rare inherited disorder, where the body's immune system mistakenly attacks platelets, leading to decreased platelets and increased bleeding risk.
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Thrombotic Thrombocytopenic Purpura (TTP)
Thrombotic Thrombocytopenic Purpura (TTP)
A serious, life-threatening condition involving platelet-mediated thrombosis, often triggered by exposure to certain drugs. It's characterized by a low platelet count, microangiopathic hemolytic anemia, fever, and neurological symptoms.
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Thrombocytopenia
Thrombocytopenia
A group of disorders characterized by a decreased number of platelets or platelet dysfunction, increasing the risk of bleeding.
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Pernicious Anemia
Pernicious Anemia
A type of anemia caused by an inability of the body to absorb vitamin B12, a key nutrient for red blood cell production.
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Inherited Red Blood Cell Disorders
Inherited Red Blood Cell Disorders
Inherited blood disorders affecting red blood cells, leading to anemia. These disorders are characterized by abnormal red blood cell shape, leading to premature destruction of these cells.
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Hereditary Spherocytosis
Hereditary Spherocytosis
A rare inherited disorder affecting red blood cells, leading to a breakdown of these cells, often resulting in iron deficiency anemia.
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Platelet Activation
- Platelets are activated through a series of steps including adhesion, aggregation, secretion, and eicosanoid synthesis.
- Platelet activation involves G proteins and the inositol triphosphate-diacylglycerol pathway.
- Platelet adhesion involves binding to the vascular matrix, facilitated by plasma membrane receptors.
- Platelet aggregation is driven by interactions between platelet surface receptors.
- Eicosanoid synthesis is crucial to the activation process.
Acute Chest Syndrome
- Acute chest syndrome is a serious condition, characterized by features such as inflammation or infection of the lungs.
- Management includes components and concentrates, monitoring therapy, plasma therapy, platelet concentrates, and RBC transfusions.
Acute Coagulopathy of Trauma-Shock
- Characterized by the presence of coagulopathies following trauma or shock.
- Causes include various factors leading to abnormal blood clotting.
- Incidence varies.
- Management focuses on various treatment components.
- Includes plasma therapy, platelet concentrates, and RBC transfusions.
Acute Leukemias
- Acute leukemias are a group of cancers affecting blood-forming cells.
- Include acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML).
- Acute leukemias of ambiguous lineages exist.
- Different classification schemes exist such as the WHO classification.
- Cytochemical stains and interpretations are used for diagnosis.
Acute Lymphocytic Leukemia (ALL)
- A type of acute leukemia with certain cytogenetic features, immunophenotypes, and morphology.
- Prognosis varies depending on the type.
- Sudan Black B staining is characteristic.
Acute Myeloid Leukemia (AML)
- A type of acute leukemia characterized by clinical presentation and specific cytogenetic features.
- May present with or without maturation.
- Can involve myelodysplasia-related changes.
- AML is associated with myelodysplasia.
- Subtypes of AML exist, including acute myelomonocytic leukemia
Adaptive Immunity
- Part of the body's immune response.
Adenosine Diphosphate (ADP)
- Plays a role in platelet aggregation.
- Involved in various blood disorders.
Anemia
- A condition characterized by a deficiency in red blood cells or hemoglobin.
- May result from various factors.
- A variety of conditions can cause anemia including aplastic anemia, anemia of chronic disease, and chronic kidney disease anemia.
- Evaluation includes a variety of tests.
- Aplastic anemia has both inherited and acquired forms.
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