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Clinical Pathology 2
Term | Definition |
---|---|
Hematopoiesis | Refers to the production of blood cells and platelets |
Thrombocytes | Another term for platelets |
Erythropoiesis | The production of erythrocytes |
Leukopoiesis | The production of leukocytes |
Thrombopoiesis | The production of platelets |
Pluripotent Stem Cells | Stem cells that are capable of developing into various types of cells (like any blood cells) |
Cytokine | A development pathway that is determined by interactions with chemical messengers (in relation to pluripotent stem cells) |
Erythropoietin (EPO) | Primary cytokine responsible for red blood cell production |
-penia | Refers to a decreased number of cells in the blood |
Neutropenia | Decreased number of neutrophils |
Lymphopenia | Decreased number of lymphocytes |
Pancytopenia | Decreased numbers of all blood cell types |
-philia or -cytosis | Refers to an increased number of cells in the blood |
Neutrophilia | Increased number of neutrophils |
Leukocytosis | Increased number of leukocytes |
Left Shift | Refers to an increased number of immature neutrophils |
Leukemia | Neoplastic cells in the blood or bone marrow; is often described with terms like leukemic, subleukemic, or aleukemic to indicate the tendency for neoplastic cells to be released in the blood |
Leukemoid Response | Conditions that can be mistaken for leukemia; characterized by leukocytosis and is usually the result of an inflammatory disease |
Anticoagulant | Prevents or delays the clotting of blood |
Plasma | The fluid portion of whole blood in which cells are suspended; roughly 90% water and 10% dissolved constituents (like proteins, carbohydrates, vitamins, hormones...) |
Serum | Plasma from which fibrinogen, a plasma protein, has been removed; when blood clots, the fluid that is squeezed out around the cellular clot is serum |
Polycythemia | An increased number of circulating red blood cells; accompanied by an increased packed cell volume and hemoglobin concentration |
Anemia | A decrease in the oxygen-carrying capacity of the blood, usually as a result of decreased numbers of circulating red blood cells |
Buffy Coat | A whitish-gray layer that sits just above the red blood cell layer in a microhematocrit tube after centrifugation; consists of white blood cells and platelets |
Lipemic | Used to describe cloudy serum |
Icteric | Used to describe plasma that has a deep yellow color; seen in animals with liver disease or hemolytic anemia |
Hemoglobin | The functional unit of the erythrocyte |
Oxyhemoglobin | Hemoglobin that is bound to oxygen |
What are the 3 erythrocyte indices? | Mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), and mean corpuscular hemoglobin concentration (MCHC). |
Mean Corpuscular Volume (MCV) | The measure of the average size of the erythrocytes |
Mean Corpuscular Hemoglobin (MCH) | The mean weight of hemoglobin contained in the average red blood cell |
Mean Corpuscular Hemoglobin Concentration (MCHC) | The concentration of hemoglobin in the average erythrocyte (or the ratio of the weight of hemoglobin to the volume in which it is contained) |
Megathrombocytes | Unusually large platelets |
Pelger-Huet Anomaly | A congenital hereditary defect that is characterized by the hyposegmentation of all granulocyte nuclei |
Macrocytosis | A mean corpuscular volume greater than 100 fL |
Toxic Granulation | Intensely stained primary granules |
Atypical Lymphocytes | May have basophilic cytoplasm and cleaved nuclei; may show evidence of asynchronous maturation of the nucleus and cytoplasm |
Reactive Lymphocytes | Have increased basophilia in the cytoplasms; may have more abundant cytoplasm and sometimes contain a larger and more convoluted nucleus; also referred to as immunocytes |
Smudge Cells | Degenerative leukocytes that have ruptured; sometimes called basket cells |
Karyolysis | Degenerative change to the nucleus that is characterized by the dissolution of the nuclear neutrophils |
Pyknosis | Refers to the condensing of the nucleus as the cell dies |
Karyorrhexis | Refers to the fragmentation of the nucleus after cell death (apoptosis) |
Rouleaux Formation | Involves the grouping of erythrocytes in stacks |
Autoagglutination | Occurs in immune-mediated disorders in which antibody coats the erythrocyte, which results in the bridging and clumping of red blood cells |
Anisocytosis | Variation in the size of red blood cells |
Hypochromasia | Decreased staining intensity caused by an insufficient amount of hemoglobin within the cell |
Anulocytes | Bowl-shaped cells |
Torocytes | "Punched-out" cells |
Poikilocytosis | Should only be used when morphologic abnormalities can be described with more specific terms (poikilocytes are abnormally shaped erythrocytes) |
Schistocytes | Red blood cell fragments; formed as a result of the shearing of the red blood cell via intravascular trauma |
Acanthocytes | Irregular, speculated red blood cells with a few unevenly distributed surface projections of variable length and diameter; also called spur cells |
Echinocytes | Spiculated cells with numerous short, evenly spaced blunt to sharp surface projections of uniform size and shape; also called burr cells |
Drepanocytes | Believed to be an in vitro phenomenon caused by high oxygen tension; also called sickle cells |
Target Cells or Codocytes | Leptocytes with a central area of pigment surrounded by a lear area and then a dense ring of peripheral cytoplasm |
Daryocytes | teardrop-shaped cells seen with myelofibrosis and other myeloproliferative diseases |
Basophilic Stippling | The presence of small, dark-blue bodies within the erythrocyte |
Howell-Jolly Bodies | Basophilic nuclear remnants that are seen in young erythrocytes during the response to anemia |
Heinze Bodies | round structures that represent denatured hemoglobin and are caused by certain oxidant drugs or chemicals |
Reticulocytes | Immature erythrocytes that contain organelles that are lost as the cells mature |
What are they types of needles that can be used for bone marrow collection? | Rosenthal, Illinois sternal, and jamshidi |
Erythrocyte Sedimentation Rate | The rate at which erythrocytes will fall in their own plasma |
Hypercellular | Increased cellularity |
Hypocellular | Decreased cellularity |
Aplasia | Less than 25% myeloid cells |
Basophilic Hyperplasia | Basophilia in bone marrow and peripheral blood |
Dyserythropoiesis | Abnormal erythrocyte maturation |
Dysgranulopoiesis (Dysmyelopoiesis) | Abnormal granulocyte maturation |
Dysmegakaryopoiesis (Dysthrombopoiesis) | Abnormal megakaryocytic or thrombocyte maturation |
Eosinophilic Hyperplasia | Eosinophilia in bone marrow and peripheral blood |
Erythroid Hyperplasia | Normal or increased cellularity with a normal or increased absolute neutrophil count and a low M:E ratio |
Erythroid Hypoplasia | Normal or decreased cellularity with a normal or decreased absolute neutrophil could and a high M:E ratio |
Granulocytic Hyperplasia | Normal or increased cellularity with a normal or increased PCV and a high M:E ratio |
Hyperostosis | Thickening of cortical bone |
Hypocellular | Decrease in overall cellularity |
Megakaryocytic Emperipolesis | Presence of intact, viable blood cells within the cytoplasm of megakaryocytes |
Megakaryocytic Hyperplasia | Increase in numbers of megakaryocytic in bone marrow |
Monocytic Hyperplasia | Increased presence of precursor cells of the monocyte series |
Myelodysplasia | Atypical cells with less than 30% blast cells present |
Myelofibrosis | Increased presence of fibrous tissue that displaces hematopoietic tissue |
Neoplasia | Atypical cells with more than 30% blast cells present |
Neutrophilic Hyperplasia, Effective | Neutrophilia in bone marrow and peripheral blood |
Neutrophilic Hyperplasia, Ineffective | Neutrophilia in bone marrow concurrent with neutropenia in peripheral blood |
Ostersclerosis | Thickening of trabecular bone |
Reactive Macrophage Hyperplasia | Increased presence of active macrophages, often containing phagocytized material |
Fibrinous Inflammation | Involves the infiltration of the bone marrow with fibrin exudate without the presence of inflammatory cells |
Chronic Inflammation | A hyperplastic condition characterized by increased numbers of plasma cells, mature lymphocytes, and mast cells |
Chronic Granulomatous Inflammation | Characterized by increased numbers of macrophages |
Chronic Pyogranulomatous Inflammation | When both macrophages and neutrophils are present |
Microparticles | Membrane-bound cytoplasmic fragments that are released from platelets, leukocytes, and endothelial cells that serve to increase the surface area on which coagulation complexes can form |
Phosphatidylserine (PS) | Acts as a binding site for the complexes of the coagulation cascade, which activates Factor X and Factor II |
Thrombocytopenia | A decrease in the circulating platelet mass; the most common coagulation disorder in small animal veterinary medicine |
Thrombocytosis | An increase in the circulating platelet mass |
Thrombopathia | Refers to abnormal platelet function |
Mean Platelet Volume (MPV) | The mathematical average of the size of individual platelets counted by the analyzer |
Plateletcrit (PCT) | A measure of the percentage of the total blood volume that is comprised of platelets |
Platelet Distribution Width (PDW) | Assesses variations in the size of the platelets |
Platelet-Large Cell Ratio (P-LCR) | A measure of the percentage of platelets that are larger than normal |
Buccal Mucosa Bleeding Time (BMBT) | A primary assay for the detection of abnormalities in platelet function |
Activated Clotting Time (ACT) | Can evaluate every clinically significant clotting factor except factor VII |
Activated Partial Thromboplastin Time (APTT) | Evaluates the intrinsic and common clotting mechanisms |
Prothrombin Time Test (PT) | Evaluates the extrinsic and common coagulation pathways; also known as one-stage prothrombin time tests (OSPT) |
Clot Retraction Test | Allows for the evaluation of platelet number and function and of intrinsic and extrinsic pathways |
PIVKA | Refers to proteins that are induced (invoked) by the absence of vitamin K |
What is the most common inherited coagulation factor deficiency in dogs? | Hemophilia A - factor VIII |
Von Willebrand Disease (vWD) | The most common inherited coagulation disorder of domestic animals |
Reference Ranges | Normal values; a range of values that have been derived when a laboratory has repeatedly assayed samples from a significant number of clinically normal animals of a given species via specific test methods |
Spectrophotometers | Designed to measure the amount of light transmitted through a solution |
Beer's Law | States that a direct linear relationship exists between the concentration of an analyze and light absorption when monochromatic light is passed through the sample |
Hyperproteinemia | Elevated total protein concentrations (commonly seen in dehydrated animals) |
Hypoproteinemia | Decreased total protein concentrations (commonly seen in over hydrated animals) |
Acute-Phase Proteins | Primarily produced by hepatocytes immediately following injury or inflammation |
Uric Acid | A metabolic by-product of nitrogen catabolism; found mainly in the liver. |
Fractional Clearance/Excretion of Electrolytes | A mathematical manipulation that describes the excretion of specific electrolytes relative to the GFR |
Enzymuria | Refers to the presence of enzymes in the urine; includes urinary GGT and urinary N-acetyl-B-d-glucosaminidase (NAG) |
Electrolytes | The negative ions and positive ions of elements that are found in all body fluids of all organisms |
Anions | Negative ions |
Cations | Positive ions |
Acid-Base Balance | Refers to the steady state of the pH of the body |
Acidosis | When the pH of body fluids is less than 7.3; characterized by excess hydrogen ions |
Alkalosis | When the pH of body fluids is more than 7.4; characterized by a low hydrogen ion concentration |
Buffers | Substances that can alter the hydrogen ion concentration |
Hypercapnia | An increased partial pressure of carbon dioxide (PCO2) in the blood |
Hypocapnia | A subsequent decrease in PCO2 in the blood |
Base Excess | The amount of strong acid or base that is required to titrate 1 L of blood to a pH of 7.4 at 37° C while the PCO2 is held constant at 40 mm Hg |
Hypernatremia | Elevated blood level of sodium |
Hyponatremia | Decreased blood level of sodium |
Hyperkalemia | Elevated plasma potassium levels |
Hypokalemia | Decreased plasma potassium levels |
Anion Gap | Any difference between the total positive charges and the total negative charges |
Lactate (Lactic Acid) | Produced by anaerobic cellular metabolism; its presence does not indicate a specific disease |
Adrenocorticotropic Hormone (ACTH) | A hormone that stimulates adrenocortical growth and secretion, particularly of glucocorticoid-synthesizing tissue |
Cortisol | The major hormone that is released in domestic mammals |
ACTH Stimulation Test | Evaluates the degree of adrenal gland response to the administration of exogenous ACTH |
Dexamethasone Suppression Tests | Evaluates adrenal glands differently by using the adrenal feedback loops |
Thyroid-Stimulating Hormone (TSH) | Enhances thyroid growth, function, and thyroxine release |
Thyroxine | Completes the regulatory cycle by inhibiting TRF and TSH release |
Melena | Black feces |
Hematochezia | The passage of fresh blood, usually in/with stool |
Plumbism | Lead poisoning |
Antigens | Any substances that are capable of generating a response from the immune system |
Inflammatory Response | A response to infection or tissue injury |
Opsonization | Refers to the binding of complement to the antigen |
Avidity | Refers to the strength of the binding of antigen and antibody and is partly the result of the affinity of the IgM for the specific antigen |
Blood Group Antigens | Specific surface markers in an individual animal that are genetically determined |
Alloantibodies | Naturally occurring antibodies (can be seen in cats, cattle, sheep, and pigs) |
Urticaria | Hives |
Wheals | A raised, itchy (pruritic) area of skin that is sometimes an overt sign of allergy; sometimes called a welt or hive |
Angioedema | Edema/swelling of the dermis and subcutaneous tissues |
Coombs Test | Detects the presence of inappropriate antibodies (antibodies against the body's own tissues) |
Polymerase Chain Reaction (PCR) | The most familiar version of a molecular diagnostic test; it detects the DNA segment of interest in the specimen submitted and amplifies its amount |
Atopy | Allergies |
Immune-Mediated Hemolytic Anemia (IMHA) | A condition that causes the destruction of red blood cells by the host itself |
Lymphoma | A type of tumor characterized by the uncontrolled proliferation of lymphocytes |