Acute & Chronic Inflammation Flashcards

1
Q

What chemicals mediate pain?

A

Prostaglandins, bradykinin, substance p

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2
Q

The absence of sialyl-lewis glycoprotein causes what disease?

A

LAD II

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3
Q

Patients with MPO deficiency often present with what?

A

Recurrent Canidia infections

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4
Q

Macrophages are seen in what type of inflammation?

A

Chronic inflammation

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5
Q

What is the primary mediator of vasodilation in acute inflammation?

A

Histamine

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6
Q

What immune cells are most prominent in acute inflammation?

A

Neutrophils

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7
Q

What protein mediates the transmigration of leukocytes from across the endothelium?

A

PECAM-1

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8
Q

What enzyme is defective in Chronic Granulomatous disease?

A

NADPH Oxidase - cannot form ROS

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9
Q

What is the clinical presentation of LAD II?

A

Shore stature, developmental delay, recurrent infections, leukocytosis

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10
Q

What are the characteristics of purulent/suppurative inflammation?

A

Exudate of pus filled with neutrophils caused by bacterial infection

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11
Q

What cytokine stimulates monocytes to divide?

A

IL-6

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12
Q

A patient presents with an ulcerative lesion, but no pus is present. What immune disorder may they have?

A

Leukocyte adhesion deficiency (LAD)

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13
Q

What receptors mediate leukocyte rolling?

A

Selectins

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14
Q

What is the function of MPO?

A

Forms hypochlorous acid that amplifies the effects of ROS

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15
Q

What chemicals mediate leukocyte adhesion and activation?

A

IL-1, TNF, chemokines, complement, Leukotrienes

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16
Q

How can MPO deficiency and Chronic Granulomatous disease be differentiated in a laboratory?

A

NPT is normal in MPO deficiency, but colorless in Chronic Granulomatous disease

17
Q

Scarring of tissue by fibrin is a form of what type of acute inflammation?

A

Fibrous inflammation

18
Q

What protein on leukocytes binds to selectins?

A

Sialyl-Lewis X-modified glycoprotein

19
Q

Integrins mediate what process of leukocyte activation in acute inflammation?

A

Adhesion to endothelium

20
Q

What is the clinical presentation of LAD I?

A

Delayed umbilical cord separation, omphalitis (inflammation of umbilicus), periodontitis

21
Q

A patient has defects in phagolysosomal fusion that increases susceptibility to pyogenic infections. What defect is present? What is the name of the disorder?

A

Mutation in CHS1/LYST gene - Chediak-Higashi Syndrome

22
Q

Epitheliod cells play a role in what type of diseases?

A

Granulomatous diseases

23
Q

Friction blister is a form of what type acute inflammation?

A

Serous inflammation - separation of dermis and epidermis by serous effusion

24
Q

What is the clincal presentation of Chediak-Higashi syndrome?

A

Oculocutaneous albinism, defective primary hemostasis, coagulation defect s (easy bruising)

25
Q

What causes LAD I?

A

Deficiency/defect in b-2 integrin (CD18)

26
Q

What is the hallmark of chronic inflammation?

A

Tissue destruction

27
Q

What are the three components of acute inflammation?

A

Vasodilation, increased vascular permeability, emigration of leukocytes

28
Q

Histamine, serotonin, and complement mediate what response in acute inflammation?

A

Vascular permeability