1/62
Vocabulary practice flashcards based on the Hematology 2 Lecture Guide for MT Licensure Exams.
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai |
|---|
No analytics yet
Send a link to your students to track their progress
Hemostasis
The maintenance of blood flow within the vascular system.
CTAD
An acronym for an anticoagulant containing citrate, theophylline, adenosine, and dipyridamole, used for coagulation tests and assays such as PF4 (plateletfactor−4) and β-TG (beta−thromboglobulin).
Sodium Citrate Volume Adjustment Formula
The formula used for patients with high hematocrit (>55 \text{%}) is C=(1.85×10−3)(100−H)V, where C is the volume of sodium citrate in milliliters, V is the total volume of blood-anticoagulant solution, and H is the hematocrit in percent.
Petechiae
Small, pinpoint hemorrhages into the skin.
Purpura
Hemorrhages into the skin that are larger than petechiae.
Ecchymosis
Also known as a bruise; a type of hemorrhage into the skin.
Epistaxis
A medical term for a nosebleed.
Hemarthrosis
Hemorrhage into a joint.
Hemoptysis
The expectoration of blood from some part of the respiratory tract.
Hematemesis
The vomiting of blood.
Menorrhagia
Unusually heavy or prolonged menstrual periods.
Hematochezia
The passage of fresh blood per anus, usually in or with stools.
Melena
The passage of black, tarry stools.
Thrombosis
The pathological formation of blood clots in veins or arteries that obstruct blood flow.
Hypofibrinogenemia
Reduced levels of fibrinogen in the blood.
Dysfibrinogenemia
A condition where fibrinogen does not function normally or optimally.
Tunica Intima
Also known as tunica interna; the innermost coat of a blood vessel composed of simple squamous epithelium lining the lumen.
Tunica Media
The thickest coat of a blood vessel, composed of smooth muscle and elastic fibers.
Tunica Adventitia
Also known as tunica externa; composed of fibrous connective tissue containing autonomic nerve endings and the vasa vasorum.
Vasa Vasorum
Small networks of blood vessels that supply nutrients to the tissues of the vessel wall.
Sinusoids
Specialized types of capillaries found in locations such as the bone marrow, spleen, and liver.
Prostacyclin (PGI2)
A substance produced by the eicosanoid pathway in endothelial cells that inhibits platelet activation and is also known as Prostaglandin I2.
Thrombomodulin (TM)
A thrombin cofactor on endothelial cells that binds thrombin, reducing its clotting ability and activating Protein C and TAFI.
von Willebrand Factor (VWF)
A protein synthesized in endothelial cells and megakaryocytes that mediates platelet adhesion and stabilizes Factor VIII.
ADAMTS 13
Also known as VWF-cleaving protease; a plasma enzyme that regulates the size of circulating VWF by cleaving ultra-long VWF multimers into shorter segments.
Thrombocytes
Another name for platelets, which arise from bone marrow megakaryocytes and have a life span of 9.0 days ±1 day.
Reticulated Platelets
Also known as stress platelets; newly released platelets that still contain RNA and are larger than usual platelets (diameter>6 νm).
Mean Platelet Volume (MPV)
The average volume of individual platelets in a specimen, with a reference range of 8 to 12 fL.
Chromomere
The granular and central part of the platelet cytoplasm when viewed on a Wright-stained peripheral blood smear.
Hyalomere
The clear and peripheral part of the platelet cytoplasm when viewed on a Wright-stained peripheral blood smear.
Thrombopoietin (TPO)
Also known as c-Mpl ligand; the humoral factor produced primarily by the liver that stimulates megakaryocytopoiesis and platelet production.
Endomitosis
A process of nuclear division without cytoplasmic division, resulting in a polyploid nucleus.
MK-I stage
The megakaryoblast stage; the least differentiated megakaryocytic precursor which begins to develop α-granules and the demarcation system.
Shedding (Thrombocytopoiesis)
The process by which one megakaryocyte may release 2,000 to 4,000 platelets.
Glycocalyx
The outer membrane surface of a platelet that contains glycoproteins and absorbs plasma proteins like albumin and fibrinogen.
Integrin αIIbβ3
Also known as GP IIb/IIIa; the key fibrinogen receptor necessary for platelet aggregation.
Integrin α2β1
Also known as GP Ia/IIa; a membrane receptor that binds to collagen.
Tenase Complex
A coagulation complex consisting of Factor 9a, platelet factor-3 (PF−3), Calcium, and Factor 8a.
Prothrombinase Complex
A coagulation complex consisting of Factor 10a, platelet factor-3 (PF−3), Calcium, and Factor 5a.
Surface-Connected Canalicular System (SCCS)
An invagination of the platelet plasma membrane that serves as a route for endocytosis and the secretion of α-granule and lysosome contents.
Dense Tubular System (DTS)
A condensed remnant of the rough endoplasmic reticulum in platelets that sequesters calcium and bears enzymes for the eicosanoid synthesis pathway.
Aspirin
Also known as acetylsalicylic acid; it blocks the synthesis of Thromboxane A2 (TXA2) by permanently acylating cyclooxygenase.
Brecher and Cronkite Method
The reference method for platelet counting using a phase-contrast microscope and 1 \text{%} ammonium oxalate as a diluent.
Platelet Lumiaggregometry
A test that measures both platelet aggregation and ATP release from dense granules using a firefly-derived luciferin-luciferase reagent.
Hereditary Hemorrhagic Telangiectasia
Also known as Rendu-Osler-Weber Syndrome; the most common inherited vascular bleeding disorder.
Ehlers-Danlos Syndrome
Also known as Cutis Hyperelastica; a disorder characterized by hyperextensible skin, hypermobile joints, and fragile tissues.
Henoch-Schonlein Purpura
Also known as Allergic Purpura; a condition most common in children involving immunologic damage to endothelial cells, gastrointestinal hemorrhage, and joint swelling.
Scurvy
A condition caused by Vitamin C deficiency, leading to defects in the synthesis of collagen and hyaluronic acid.
Bernard-Soulier Syndrome (BSS)
A platelet adhesion disorder caused by a deficiency of the GP Ib/IX/V complex.
Glanzmann’s Thrombasthenia
A platelet aggregation disorder caused by a deficiency of the GP IIb/IIIa complex.
Gray Platelet Syndrome
An alpha-granule deficiency characterized by large, gray platelets and lifelong mild bleeding tendencies.
Contact Group
A group of clotting factors comprising Factors XII, XI, Prekallikrein (PK), and High-molecular-weight Kininogen (HMWK) which are Vitamin K-independent.
INR (International Normalized Ratio)
A standardized way of reporting PT results using the formula INR=(Mean Normal PTPatient PT)ISI to correct for variations in thromboplastin sensitivity.
Warfarin
An oral anticoagulant and Vitamin K antagonist (brand name Coumadin) that interferes with the synthesis of Factors II, VII, IX, and X.
Protamine Sulfate
A protein used for neutralizing unfractionated heparin (UFH).
Activated Coagulation Time (ACT)
A point-of-care clot-based screening test useful for monitoring high dosages of unfractionated heparin.
Stypven Time
Also known as Russel’s Viper Venom Time; it is used to detect deficiencies in fibrinogen, prothrombin, and Factors V and X, but does not detect Factor VII deficiency.
Reptilase Time
A test using venom from the Bothrops atrox snake that is capable of converting fibrinogen to fibrin and is unaffected by heparin.
Thrombosthenin
A contractile protein important for clot retraction.
Euglobulin Lysis Time
A test for fibrinolysis where proteins that precipitate under acid conditions (euglobulins) are clotted with thrombin and observed for the time needed for complete lysis.
D-dimer Test
A test where the presence of D-dimer indicates that a stable, cross-linked fibrin clot has been lysed by plasmin.
Alpha-2-antiplasmin
The primary inhibitor of free plasmin in the circulation, synthesized in the liver.
TAFI
Thrombin-Activatable Fibrinolysis Inhibitor; an enzyme activated by the thrombin-thrombomodulin complex that functions as an antifibrinolytic.