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
What causes LAD I?
Deficiency/defect in b-2 integrin (CD18)
26
What is the hallmark of chronic inflammation?
Tissue destruction
27
What are the three components of acute inflammation?
Vasodilation, increased vascular permeability, emigration of leukocytes
28
Histamine, serotonin, and complement mediate what response in acute inflammation?
Vascular permeability