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N 5315 Advanced Patho Hematologic Module 4 questions with answers

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N 5315 Advanced Patho Hematologic Module 4 questions with answers

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N 5315 Advanced Patho
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Hematologic Module 4 questions /| /| /| /|




with answers /|




What is the peripheral zone of platelet? - CORRECT ANSWERS
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✔✔Outermost layer. Made of phospholipids. Contains many /| /| /| /| /| /| /|



receptors responsible for platelet adhesion and aggregation
/| /| /| /| /| /|




What is the sol-gel of the platelet - CORRECT ANSWERS ✔✔It is
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the outermost layer made of possible if it contains many receptors
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responsible for platelet adhesion and aggregation /| /| /| /| /|




What is the organelle zone of platelets - CORRECT ANSWERS
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✔✔Innermost layer contains calcium dense granules and alpha /| /| /| /| /| /| /| /|



granules


What are the four phases of platelet plug formation? - CORRECT
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ANSWERS ✔✔Activation, adherence, aggregation, and secretion
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What is the first step or phase of platelet plug formation and
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explain - CORRECT ANSWERS ✔✔Activation is the first step. In
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physiological states. Platelets circulate without adhering to the /| /| /| /| /| /| /| /|



intact endothelium. An injury to the endothelium exposes thev WF,
/| /| /| /| /| /| /| /| /|



fibronectin, collagen and from thrombospondin.. Collagen is a
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potent activator and when the sub endothelial collagen is exposed
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by an injury. The platelets become charged AKA activated.
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,Platelets and become aware of the injury and undergo a shape
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change that increases their ability to adhere to the site of injury.
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The second step in platelet plug formation is - CORRECT
/| /| /| /| /| /| /| /| /| /|



ANSWERS ✔✔Adherence is a process by which platelets attached
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to the injured endothelium. Adherence begins with the vWF.
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Circulating vWF binds to the exposed subendothelial collagen and
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to the GP Ib/IX/V receptors on circulating platelets. Collagen then
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binds with the GP VI receptor. The binding of collagen with the GP
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VI receptor results in the activation of the GPIIb/IIIa and GPIa/IIa
/| /| /| /| /| /| /| /| /| /| /|



receptors. vWF then binds with the GPIIb/IIIa receptors and
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collagen further binds with the GPIa/IIa receptors. This collective
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binding anchors the platelets in place
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The third step in platelet plaque formation is - CORRECT
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ANSWERS ✔✔Aggregation- is the process by which platelets bind
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to one other. There are multiple GPIIb/IIIa receptors on one
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platelet and when activated (as described above) they have a
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greater affinity for fibrinogen. Fibrinogen is able to bind to two
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GPIIb/IIIa receptors simultaneously and thereby bind platelets
/| /| /| /| /| /| /|



together


The fourth step in platelet plug formation is - CORRECT ANSWERS
/| /| /| /| /| /| /| /| /| /| /|



✔✔Secretion- during this phase the platelet granules release their /| /| /| /| /| /| /| /| /|



contents.
a. ADP- enhances adhesion, activates platelets and recruits
/| /| /| /| /| /| /| /|



platelets
b. Serotonin recruits platelets.
/| /| /|




c. Fibronectin and thrombospondin are proteins which stabilize
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platelets that are adhered to the site of injury.
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,d. Thromboxane A2- is a product of the arachidonic acid pathway
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but is stored inside the platelet too. It causes vasoconstriction and
/| /| /| /| /| /| /| /| /| /| /|



enhances platelet aggregation. /| /|




e. Growth factors promote tissue repair however they have a role
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in the development of atherosclerosis.
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The final step in platelet plug formation - CORRECT ANSWERS
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✔✔The platelet plug is stabilized by fibrin and XIIIa which are the
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end products of the coagulation cascade.
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What is the extrinsic pathway arms of the coagulation cascade -
/| /| /| /| /| /| /| /| /| /| /|



CORRECT ANSWERS ✔✔Extrinsic pathway is considered the /| /| /| /| /| /| /|



primary pathway of coagulation. It is activated when Tissue Factor
/| /| /| /| /| /| /| /| /| /|



is exposed at the site of injury. The process starts with a vascular
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injury which results in the exposure of Tissue Factor (III) which has
/| /| /| /| /| /| /| /| /| /| /| /|



a cell receptor for factor VII. (As a side note lipid filled
/| /| /| /| /| /| /| /| /| /| /| /|



macrophages in atherosclerotic plaques contain a large amount of /| /| /| /| /| /| /| /| /|



tissue factor which increases the likelihood of arterial thrombus
/| /| /| /| /| /| /| /| /|



formation from plaque ruptures). Once exposed TF binds with VII
/| /| /| /| /| /| /| /| /| /|



to form the TF/VIIa complex. TF/VIIa activates X = Xa. Activated
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factor Xa binds with activated Va and calcium to form the
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prothrombinase complex. The prothrombinase complex converts /| /| /| /| /| /|



factor II (prothrombin) to activated factor IIa (thrombin). Thrombin
/| /| /| /| /| /| /| /| /|



(activated factor IIa) then moves on to activate 4 factors. It
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activates factor I (fibrinogen) to activated factor Ia (fibrin) and it
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also activates factors V, VIII & XIII. You can see the action of
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thrombin on your screen marked with blue lines. Fibrin (activated
/| /| /| /| /| /| /| /| /| /|



factor Ia) is placed over the platelet plug and activated factor XIIIa
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stabilizes the fibrin. /| /|

, What is the intrinsic pathway arms of the coagulation cascade -
/| /| /| /| /| /| /| /| /| /| /|



CORRECT ANSWERS ✔✔The clinical significance of the intrinsic
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pathway is not entirely understood, because a deficiency of factor
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XII (Hageman factor) does not cause bleeding. As such the
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intrinsic pathway's main function is thought to be one which
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enhances the extrinsic pathway. This pathway is activated when
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the blood is exposed to negative charges which are found on the
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molecules of ADP and ATP. This exposure activates factor XII
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(Hageman factor). Activated factor XIIa then activates factor XI.
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Activated factor XIa activates IX. Activated factor IXa then
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activates factor X. Activated factor Xa then forms the
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prothrombinase complex in the common pathway. /| /| /| /| /|




Coagulation Cascade Key Plasma Proteins /| /| /| /| /|




1.Tissue Factor /| /|




2.VII
3.X /|




4 .Prothrombinase Complex
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5. Prothrombin
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6. Thrombin
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7 .Fibrinogen
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8. Fibrin
/|




9. XIII
/|




10. XII /|




11. VIII /|




12. IX /|




13. Antithrombin/|

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