CA1 Hematology Vocabulary Flashcards

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Comprehensive vocabulary flashcards generated from the CA1 Hematology lecture notes covering blood components, erythropoiesis, microcytic, normocytic, macrocytic anemias, and polycythemia.

Last updated 10:54 PM on 9/28/26
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22 Terms

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Hematology

The branch of medicine that studies and treats blood, blood-forming organs, and blood-related disorders.

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Convalescent Plasma Therapy

A treatment using blood plasma from recovered individuals to provide passive immunity and deliver antibodies to sick patients before their immune system responds.

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<p>Hemoglobin</p>

Hemoglobin

An iron-rich protein in red blood cells that carries oxygen from the lungs to the rest of the body.

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Hematocrit

The percentage of total blood volume occupied by red blood cells, also referred to as packed cell volume (PCV).

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Mean Corpuscular Volume (MCV)

A measurement of the average size and volume of individual red blood cells evaluated in a complete blood count.

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<p>Erythropoiesis</p>

Erythropoiesis

The process of red blood cell production occurring in red bone marrow, stimulated by erythropoietin released from the kidneys.

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Microcytic Anemia

A group of anemias characterized by red blood cells that are smaller than normal, indicated by a Mean Corpuscular Volume (MCV) under 80 fL80\,\text{fL}.

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<p>Iron Deficiency Anemia (IDA)</p>

Iron Deficiency Anemia (IDA)

A microcytic blood condition caused by inadequate iron stores, leading to decreased hemoglobin synthesis and reduced oxygen delivery to tissues.

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<p>Thalassemia</p>

Thalassemia

An autosomal recessive inherited blood disorder caused by reduced synthesis of globin chains, impairing normal hemoglobin formation.

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Alpha Thalassemia Major

The most severe form of α\alpha-thalassemia caused by the loss of all 4 alpha-globin genes, leading to hydrops fetalis and extreme fluid buildup.

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Beta Thalassemia Major (Cooley's Anemia)

The most severe form of β\beta-thalassemia manifesting in infants aged 6 to 24 months, marked by severe anemia, poor growth, bone deformities, and hepatosplenomegaly.

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Normocytic Anemia

Anemia characterized by a reduced overall quantity of red blood cells or hemoglobin, while individual red blood cells retain normal size.

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<p>Aplastic Anemia</p>

Aplastic Anemia

A rare and serious blood disorder where bone marrow failure leads to pancytopenia.

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Pancytopenia

A condition involving a simultaneous deficiency of red blood cells, white blood cells, and blood platelets.

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<p>Sickle Cell Anemia</p>

Sickle Cell Anemia

An inherited blood disorder in which abnormal hemoglobin causes round red blood cells to become rigid, C-shaped, and prone to capillary obstruction under low oxygen tension.

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Vaso-Occlusive Crisis

An acute, painful episode in sickle cell anemia caused by sickled cells obstructing blood flow in small capillaries, resulting in tissue ischemia and infarction.

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Macrocytic Anemia

A category of anemia characterized by abnormally large red blood cells, defined by a Mean Corpuscular Volume (MCV) exceeding 100 fL100\,\text{fL}.

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Pernicious Anemia

A specific type of vitamin B12 deficiency caused by an autoimmune failure of gastric parietal cells to produce intrinsic factor (IF).

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Schilling Test

A medical test performed to determine the specific cause of vitamin B12 deficiency and assess intestinal absorption capabilities.

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<p>Polycythemia Vera</p>

Polycythemia Vera

A chronic blood cancer caused by a mutation in the JAK2JAK2 gene, leading to overproduction of red blood cells and increased blood viscosity.

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<p>Erythromelalgia</p>

Erythromelalgia

A peripheral vascular condition associated with polycythemia, presenting with a classic triad of erythema, warmth, and paroxysmal burning pain in the extremities.

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Deferasirox

An iron chelation medication administered to treat iron overload resulting from repeated blood transfusions.