Chapter 3 Immunity and Immunologic Oral Lesions Flashcards

(88 cards)

1
Q

Dissolution of the intercellular bridges of the prickle cell layer of the epithelium.

A

Acantholysis

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2
Q

An immune response to a foreign substance based on the specific memory of a past exposure to the same foreign substance.

A

Acquired immune response

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3
Q

An immunity based on antibodies developed in response to an antigen, which includes both natural and acquired types.

A

Active immunity

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4
Q

The agents that can be added to a vaccine to modify the immune response.

A

Adjuvants

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5
Q

An antigen that produces a hypersensitivity or allergic reaction.

A

Allergen

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6
Q

Hypersensitivity acquired through exposure to a particular allergen that elicits an exaggerated reaction on re-exposure to the same allergen.

A

Allergy

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7
Q

A severe immediate type of hypersensitivity in which an exaggerated immunologic reaction occurs on re-exposure to a foreign protein or other substance after sensitization, resulting in not only hives, itching, and swelling, but also vascular collapse and shock, as well as death.

A

Anaphylaxis

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8
Q

A lesion that appears as a diffuse swelling of tissue caused by an increased permeability of deeper blood vessels. The skin covering the swelling appears normal.

A

Angioedema

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9
Q

A protein molecule or immunoglobulin that is secreted by plasma cells and reacts with a specific antigen; including five classes: IgA, IgD, IgE, IgG, and IgM.

A

Antibody

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10
Q

The level of antibody in the blood that can be measured by a diagnostic laboratory test.

A

Antibody titer

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11
Q

Any substance able to induce a specific immune response.

A

Antigen

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12
Q

The ability to reduce the virulence of a pathogenic microorganism but still keep it viable, as is done in the development of certain vaccines.

A

Attenuated

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13
Q

An antibody that reacts against a tissue constituent of one’s own body.

A

Autoantibody

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14
Q

An immunopathologic condition characterized by tissue trauma caused by an immune response against tissue constituents of one’s own body.

A

Autoimmune disease

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15
Q

A lymphocyte that develops in lymphoid tissue other than the thymus and that can later differentiate into a plasma cell that produces antibody, the main initiator of humoral immunity.

A

B-cell lymphocyte

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16
Q

An immunity in which the major role is played by the T-cell lymphocytes.

A

Cell-mediated immunity

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17
Q

A white blood cell that acts as an antigen-presenting cell in the skin and mucosa.

A

Dendritic cell

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18
Q

A collection of 50 or more lymphocytes clustered within the salivary gland parenchyma (1 focus = 50 or more lymphocytes). A focus score of 1 or more is compatible with a diagnosis of Sjogren syndrome.

A

Focus

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19
Q

A type of indirect protection from an infectious disease that occurs when a large percentage of the population becomes immune to the infection.

A

Herd immunity

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20
Q

An immunity in which both the B-cell lymphocytes and the antibodies they produce as plasma cells play a predominant role.

A

Humoral immunity

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21
Q

An altered state of reactivity in which the body reacts to a foreign agent such as an allergen with an exaggerated immune response; includes types I through IV.

A

Hypersensitivity

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22
Q

An induction of active immunity, such as when the pathogenic microorganism used to induce active immunity is encountered after vaccination.

A

Immunization

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23
Q

An immunopathologic condition that involves a compromised or entirely absent immune system involving its white blood cells and their products.

A

Immunodeficiency

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24
Q

The proteins secreted by plasma cells that serve as antibodies designed to respond to a specific antigen; includes IgA, IgD, IgE, IgG, and IgM.

A

Immunoglobulins

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25
An agent that alters the immune response by adding or reducing the ability of the response.
Immunomodulator
26
As a cytokine and within the family of glycoproteins, it has immunoregulatory, antineoplastic, and antiviral activity.
Interferon
27
A specialized dendritic cell found in the skin and mucosal tissue that is involved in the immune response.
Langerhans cell
28
Mature neutrophil with a phagocytized spherical inclusion derived from another neutrophil; it is used as a marker of autoimmune diseases.
LE cell
29
The white blood cells involved in the immune response that have three major subsets that include the B-cell lymphocyte, T-cell lymphocyte, and NK cell.
Lymphocytes
30
Tissue composed of lymphocytes supported by a meshwork of connective tissue, including tonsillar tissue, lymph nodes, and lymphatic organs.
Lymphoid tissue
31
The subset of cytokines produced by B-cell or T-cell lymphocytes in contact with antigens that serve as biochemical mediators in an immune response.
Lymphokines
32
A large, tissue-bound, mononuclear phagocyte derived from monocytes circulating in the blood, which can become mobile when stimulated by inflammation and interact with lymphocytes in an immune response as well as during inflammation.
Macrophage
33
A migratory cell of connective tissue that contains many granules of histamine.
Mast cell
34
The subset of cytokines primarily produced by monocytes or macrophages that serve as biochemical mediators in an immune response.
Monokines
35
Affecting both mucosal surfaces (i.e. oral and genital) and skin.
Mucocutaneous
36
The inflammation of a mucosal tissue caused by a disease process.
Mucositis
37
A lymphocyte that is part of the initial innate immune response, which by unknown mechanisms, is able to directly identify and then destroy cells recognized as foreign.
Natural killer cell
38
Diagnostic sign whereby the superficial epithelium separates easily from the basal layer on exertion of firm, sliding manual pressure with the fingers or a tongue blade.
Nikolsky sign
39
An immunity that uses antibodies produced by another person to protect an individual against infectious disease, which includes both natural immunity and acquired immunity.
Passive immunity
40
A nonspecific hypersensitivity reaction, in which a small sterile needle is inserted into the skin of the forearm. A small red bump or pustule will appear at the site of needle insertion in 1-2 days if the test is positive. May be used in the diagnosis of Bechet syndrome.
Pathergy test
41
The cell derived from B-cell lymphocytes that produce antibodies in response to the presence of antigen.
Plasma cell
42
The symptom of severe itching caused by a disease process, possibly a hypersensitivity reaction or allergy.
Pruritis
43
Antibody that binds to certain antibodies found in the serum of patients with rheumatoid arthritis and connective tissue diseases such as Sjogren syndrome. Current assays test for IgM-class rheumatoid factor.
Rheumatoid factor
44
A test that measures lacrimal gland flow by placing special filter paper strips inside the lower eyelid for 5 minutes.
Schirmer test
45
A classic example of type III hypersensitivity that involves a drug allergy to antitoxin serum from horses.
Serum sickness
46
Fibrous adhesion between the eyeball and conjunctiva.
Symblepharon
47
A group of signs and symptoms that occur together in one condition.
Syndrome
48
A lymphocyte that matures in the thymus and is mainly responsible for initiating cell-mediated immunity as well as modulating humoral immunity.
T-cell lymphocyte
49
Organ consisting of lymphoid tissue located high in the chest, which is large in an infant and gradually shrinks in size in adulthood; site of T-lymphocyte maturation.
Thymus
50
Detached rounded cells caused by a loss of attachment between epithelial cells. Also known as acantholytic cells. These cells are present with pemphigus vulgaris.
Tzanck cells
51
Multiple areas of well-demarcated swelling in the skin, usually accompanied by itching. The lesions are caused by localized areas of vascular permeability in the superficial connective tissue beneath the epithelium. Also known as hives.
Urticaria
52
Dryness of the mucous membranes, including the oral cavity; usually caused by hyposalivation or decreased salivary flow.
Xerostomia
53
Appear as “punched-out” round-to-oval ulcers up to 1 cm in diameter. Can have a white to yellow fibrin center, and are common in the anterior part of the mouth. Affect 80% of those with recurrent aphthous ulcers.
Minor aphthous ulcers
54
The smallest type of aphthous ulcer, usually 1-2mm in diameter, and the least common. They can develop anywhere in the oral cavity but are frequently on the lateral aspect of the tongue.
Herpetiform aphthous ulcers
55
Usually larger than 1 cm and are deeper and last longer than minor aphthous ulcers. They can be more painful and usually occur in the posterior part of the mouth. Less common than minor aphthous ulcers.
Major aphthous ulcers
56
Lesions that develop as result of direct contact with an allergen to the oral mucosa or the skin, respectively. Example of a type IV hypersensitivity. Mucosa will become erythematous and edematous, often accompanied by burning and pruritis, it will also be shiny and have a firm consistency.
Allergic contact mucositis/contact dermatitis
57
Lesions that appear in the same site each time a drug is introduced, they appear suddenly after a latent period of several days and then subside when the drug is discontinued. Appears as single or multiple slightly raised, reddish patched or clusters of macules on the skin but rarely the oral cavity. Type III hypersensitivity.
Fixed drug eruptions
58
Is an acute, self-limited disease that affects the skin and mucous membranes. The cause is unclear, but commonly occurs in adults under age 30, and includes a wide range of disease.
Erythema multiforme (EM)
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EM involving oral mucosa and some skin sites.
Erythema multiforme minor (EM minor)
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EM with involvement of two or more mucosal sites with widespread skin involvement.
Erythema multiforme major (EM major)
61
A chronic mucocutaneous disease, appears as an arrangement of interconnecting white lines and circles that do not rub off (lace-like pattern). Most common location is the buccal mucosa and can by asymptomatic or symptomatic.
Lichen planus
62
Composed of Whickham striae along with slightly raised white plaque like areas that do not rub off. Often found bilateral on the buccal mucosa, but the tongue, palate, and gingiva may be involved too.
Reticular lichen planus
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Forms in which the epithelium separates from the connective tissue, resulting in erosions, bullae, or ulcers. These are less common.
Erosive lichen planus/bullous lichen planus
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Lichen planus that can also present with red, erosive, peeling gingival lesions, a clinical term, not a specific diagnosis.
Desquamative gingivitis
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A condition in which lesions clinically and histopathologically resemble lichen planus but do not fully meet either characteristic or histopathologic features. Composed of a mixed inflammatory infiltrate rather than only lymphocytes and may extend deeper into connective tissue.
Lichenoid mucositis
66
A chronic, systemic, autoimmune disease that only affects the salivary and lacrimal glands, resulting in a decrease in saliva and tears.
Sjogren syndrome/sicca syndrome
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Dry eyes
Xerophthalmia
68
Damage to the eyes from a reduced lacrimal flow.
Keratoconjunctivitis sicca
69
Salivary and lacrimal gland involvement without the presence of another autoimmune condition.
Primary Sjogren syndrome
70
When another autoimmune disease accompanies salivary and lacrimal involvement, 50% of those with Sjogren syndrome have another autoimmune condition.
Secondary Sjogren syndrome
71
Occurs in patients with Sjogren syndrome, is a circulatory disorder affecting the fingers and toes. Cold and stress trigger the condition, and skin has a pallor from vasoconstriction followed by cyanosis from decreased blood flow.
Raynaud phenomenon
72
An acute and chronic inflammatory autoimmune disease of unknown cause. Genetic and environmental factors have an influence on the pathogenesis of the disease. Occurs more frequently in women, specifically Black women in childbearing years.
Systemic lupus erythematosus
73
A severe, progressive autoimmune disease that affects the skin and mucous membranes. Characterized by intraepithelial vesicle formation that results from breakdown of the cellular adhesion between epithelial cells.
Pemphigus vulgaris
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A chronic autoimmune disease that affects the oral mucosa, conjunctiva, genital mucosa, and skin. Occurs in women over 50 years and is not as serious as pemphigus vulgaris. The worst complication is symblepharons.
Mucous membrane pemphigoid/cicatricial pemphigoid/benign mucous membrane pemphigoid
75
A chronic, recurrent, and multisystem autoimmune disease. The manifestations of the syndrome are the result of systemic vasculitis. The pathogenesis is unclear, but oral ulcers, genital ulcers, and ocular inflammation are common manifestations. Skin lesions, GI and genitourinary disease, arthritis, and CNS involvement can occur as well.
Behcet syndrome
76
Manifestation of sarcoidosis, red-to-purple-colored indurated lesions on the skin.
Lupus pernio
77
A type of skin inflammation seen in the lower extremities as a manifestation of sarcoidosis.
Erythema nodosum
78
Are immunodeficiencies of genetic or developmental origin and can involve B cells, T cells, or both.
Primary immunodeficiencies
79
The most common primary immunodeficiency. Effects primarily those of European ancestry, characterized by low levels of both serum and secretory IgA. There is impaired differentiation of B lymphocytes to IgA-producing plasma cells. Results in susceptibility to respiratory, GI, and GU infections. Also increased risk of respiratory allergy, systemic lupus erythematous, and RA.
Isolated IgA deficiency
80
A disorder in which B-cell precursors stop maturing before they complete immunoglobulin gene development. As result plasma cells are deficient and there is a lack of immunoglobulins. Occurs almost always in males and is evident at 6 months old.
Bruton disease
81
A group of genetically inherited syndromes that have defects in both humoral and cell-mediated responses. Infants with these syndromes present with recurrent, severe infections by a wide range of pathogens.
Severe combined immunodeficiency
82
Is a primary immunodeficiency characterized by defects in function of neutrophils. Neutrophils are not able to migrate and are not able to phagocytose and destroy bacteria. This results in persistent bacterial infections, including gingival and periodontal infections.
Leukocyte adhesion deficiency
83
Those that occur as a result of an underlying disorder. Much more common than primary immunodeficiency disorders.
Secondary immunodeficiencies
84
Drugs used to suppress the immune system, like radiation, corticosteroids, drugs used to treat autoimmune disorders, etc.
Immunosuppressive drugs
85
Lack of proper nutrition, caused by not having enough to eat, not eating enough of the right things, or being unable to use the food that one does eat. Causes a physical imbalance.
Malnutrition
86
Disease that involves the renal system (i.e. kidneys).
Renal diseases
87
A virus that attacks cells that help the body fight infection, making a person more vulnerable to other infections and diseases. Will eventually develop into AIDS.
HIV infection
88
A disease that occurs when blood glucose is too high. The body doesn’t make enough insulin or has a resistance to insulin, causing poor regulation of blood glucose. Too much glucose then stays in the blood, and not enough reaches the cells of the body.
Type II diabetes