Path Chapter 3

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Created by:

JHuguelet  on September 13, 2011

Subjects:

dental-hygiene

Description:

Immunity

Classes:

oral path, Oral Pathology

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Path Chapter 3

acantholysis
dissolution of the intercellular bridges of the prickle cell layer of the epithelium
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Terms

Definitions

acantholysis dissolution of the intercellular bridges of the prickle cell layer of the epithelium
acquired immune response a response fo the body to injury that has memory of past exposure to a foreign substance and responds more quickly to a foreign substance when encountered a second time
allergy a hypersensitive state scquired through exposure to a particular allergen; reexposure to the same allergen elicits an exaggerated reaction
anaphylaxis a severe type of hypersensitivity or allergic reaction in which the exaggerated immunologic reaction results from the release of vasoactive substances such as histamine; the reaction occurs on reexposure to a foreign protein or other substance after sensitization
antibody a protein molecule, also called an immunoglobulin, which is produced by plasma cells and reacts with a specific antigen
antigen any substance able to induce a specific immune response
autoantibody an antibody that reacts against an antigenic constituent of the person's own tissues
autoimmune disease a disease characterized by tissue injury caused by a humoral or cell-mediated immune response against constituents of the body's own tissues
B lymphocyte (B cell) a lymphocyte, that matures without passing through the thymus; the B cell can later develop into a plasma cell that produces antibodies
cell-mediated immunity immunity in which the predominant role is played by T lymphocytes
cytokine cell product produced by the cells involved in the immune response
humoral immunity immunity in which B lymphocytes and antibodies play the predominant role
hypersensitivity a state of altered reactivity in which the body reacts to a foreign agent with an exaggerated immune response
immune complex a combination of antibody and antigen
immunodeficiency a deficiency of the immune response resulting from hypoactivity or decreased cumbers of lymphoid cells
immunoglobulin (Ig) a protein, also called an antibody, synthesized by plasma cells in response to a specific antigen
LE cell a cell that is a characteristic of lupus erythematosis and other autoimmune diseases; it is a mature neutrophil that has pahocytized a spherical inclusion derived from another neutrophil
lymphoid tissue tissue composed of lymphocytes supported by a meshwork of connective tissue
macrophage a large tissue-bound mononuclear phagocyte derived from monocytes circulating in blood; they become mobile when stimulated by inflammation and interact with lymphocytes in an immune response
mucositis mucosal inflammation
natural killer cell (NK cell) a lymphocyte that is part of the body's initial innate immunity, which by unknown mechanisms is able to directly destroy cells recognized as foreign
Nikolsky's sign in some bullous disease such as pemphigus vulgaris and bullous pemphigus the superficial epithelium separates easily from the basal layer on exertion of firm, sliding manual pressure
rheumatoid factor a protein, IgM, found in serum and detectable on laboratory tests; it is associated with rheumatoid arthritis and other autoimmune diseases
T lymphocyte (T cell) a lymphocyte that matures in the thymus before migrating to tissues; it is responsible for cell-mediated immunity and may modultate the humoral immune response
thymus a lymphoid organ located high in the chest, which is large in an infant and gradually shrinks in size
xerophthalmia abnormal dryness of the eyes
xerostomia patient complaint of dryness of the mouth usually caused by decreased salivary flow
minor aphthous ulcerE: trauma most common; unclear immunologic pathogenesis
a/r/s: more common in younger and women
L: oral mucosa not covering bone; ant more than post
C: painful, discrete, round to oval yellow-white ulcers, halo of erythema, <= 1 cm in diam
Tx: topical corticosteroids; spontaneous healing in 7-10 days
Dx: clinical
Major aphthous ulcer E: unclear immunologic pathogenesis
L: oral mucosa not covering bone; often in posterior
C: painful, >1 cm in diam; often deeper; may last several weeks; often heal with scarring
Tx: topical or systemic corticosteroids; biopsy for differential Dx
Dx: clinical, microscopic
herpetiform aphthous ulcers E: unclear immunologic pathogenesis
L: anywhere in oral cavity
C: painful, very tiny 1-2 mm ulcers; often occurs in groups
Tx: resolve spontaneously; topical corticosteroids; topical tetracycline
Dx: clinical
Urticaria (hives)E: type I hypersensitivity; release of IgG, IgM, ingested allergen, trauma, emotional stress, localized vascular permeability in superficial CT
L: skin
C: multiple areas of well-demarcated swelling with pruritus
Tx: self-limiting episodes; identification & avoidance of causative agent; antihistamine
Dx: clinical
angioedema E: Type I hypersensitivity, trauma, release of IgG, IgM; permeability of deeper blood vessels
L: skin or mucosa
C: diffuse swelling of tissue; usually no itching
Tx: self-limiting episodes; identification of causative agent; antihistamine
Dx: clinical
contact mucositis E: direct contact of allergen with mucosa
L: mucosa in contact with allergen
C: smooth, shiny, firm mucosa with erythema & edema; may form vesicles; often itching or burning sensation
Tx: ID of causative agent; topical and systemic corticosteroids
Dx: clinical
contact dermatitis E: direct contact of allergen with skin
L: skin in contact with allergen
C: erythema, swelling vesicles to encrusted, scaly, white appearance
Tx: ID of causative agent, topical and systemic corticosteroids
Dx: clinical
fixed drug eruptionsE: type III hypersensitivity
L: same site each episode; usually skin but occasionally oral mucosa
C: lesions appear when drug is introduced and subside when discontinued with increasing intensity; single to multiple raised, reddish patches or clusters of macules; pain/ pruritus may be present
Tx: ID & discontinuation of causative drug
Dx: clinical
erythema multiformeE: unclear; evidence for hypersensitivity reaction
a/r/s: young adults; men
L: skin and mucous membranes
C: SKIN - characteristic target lesion, also macules, plaques, bullae; MUCOSA - erythema, ulcers, crusted, bleeding lips
Tx: ID of causative agent if possible; topical/ systemic corticosteroids
Dx: clinical
Stevens-Johnson syndrome severe form of erythem multiforme; explosive onset
lichen planusE: unknown
a/r/s: broad age range, but increased prevalence in middle age, women
L: skin and oral mucosa lesions; oral mucosa: buccal, tongue, labial, floor of mouth, gingiva
C: ORAL LESIONS - erosive and plaquelike lesions may occur; Wickham's striae; GINGIVAL - desquamative gingivitis
Tx: None (if asymptomatic); topical corticosteroids (if symptomatic); follow up eval
Dx: clinical, microscopic
Reactive Arthritis (Reiter Syndrome)E: abnormal immunologic response to infectious agent; genetic influence (presence of HLA-B27)
a/r/s: men affected 10-15:1 compared to women
L: conjunctiva, urethra, oral mucosa, skin, knee & ankle joints
C: syndrome triad; arthritis, urethritis, conjunctivitis, skin lesions, oral lesions, aphthouslike ulcers; lesions resembling geographic tongue
Tx: ASA & NSAIDs
Dx: clinical
Sjogren syndrome E: autoimmune disease; decreased lacrimal & salivary flow
L: eyes & oral cavity
C: xeropthalmia, xerostomia
Tx: saliva substitutes, saliva stimulation, pilocarpine
Dx: clinical, radiographic, microscopic, laboratory
Systemic Lupus Erythematosus (SLE)E: autoimmune disease
a/r/s: women 8:1 over men, blacks 3:1 over whites
L: multiple sites - skin, mucous membranes, joints, eyes, CNS, kidneys, heart, others
C: oral lesions; erythematous plaques or erosions; white striations radiating from center of lesion
Tx: antiinflammatory & immunosuppressive agents
Dx: laboratory, microscopic, clinical
Pemphigus VulgarisE: autoimmune disease
a/r/s: children & adults; most common in 4th or 5th decade, more common in Ashkenazic Jews
L: mucous membranes; skin
C: progressive involvement of mm & skin; oral lesions; painful, wrythema, vesicles, bullae, erosions; positive Nikolsky's sign
Tx: corticosteroids and other immunosuppressive agents
Dx: laboratory, microscopic
benign mucous membrane pemphigoid E: autoimmune disease
a/r/s: adults
L: mucous membranes (gingiva most common) may affect eyes
C: oral lesion; desquamative gingivitis, bullae, erosions, ulcers, lesions heal with scarring
Tx: topical/ systemic corticosteroids
Dx: microscopic
Behcet Syndrome E: autoimmune disease
a/r/s: mean age of onset is 30
L: mucous membranes, oral, genital, ocular
C: oral lesions; aphthouslike ulcers
Tx: corticosteroids and other immunosuppressive agents
Dx: clinical
antigens the immune system usually defends the body against foreign substances that are called:
It allows faster immune responses Memory is an important function of the immune system because:
producing active acquired immunity immunization with a vaccine works by:
is derived from a precursor stem cell A B lymphocyte is a cell in the immune system that:
can be activated by lymphokines A macrophage is a cell in the immune system that:
NK cells are part of the body's innate immunity Which statement is true of NK cells?
NK cells do not circulate
NK cells secrete antibodies
NK cells are part of the body innate immunity
NK cells are T lymphocytes
autoimmune disease In which type of immunopathologic disease are the cells of the body no longer tolerated and treated by the immune system as antigens?
produce antibody called IgE During the anaphylactic type of hypersenitivity reaction, the plasma cells:
Type II Which type of hypersensitivity reaction involves activated complement?
T lymphocyte What type of lymphocyte matures in the thymus, produces lymphokines, and can increase or suppress the humoral immune response?
also called immunoglobulins In the immune system, antibodies are proteins that are:
immunodeficiency Which type of immunologic disease involve a decreased number or activity of lymphoid cells?
antibodies The humoral immune response involves the production of:
titer The measurement of a spcific antibody level in the blood is called:
acquired passive immunity Which type of immunity may be provided immediately to dental personnel after needlestick accidents?
use with children Which of the following situations would result in the least risk of drug allergy?
application of topical medication
presence of infection
presence of multiple allergies
use with children
cell mediated immunity which of the following is involved in the regulation of both humoral and cell-mediated immunity?
humoral immunity
cell-mediated immunity
innate immunity
the bone marrow
cytokines which of the following is involved in the communication between lymphocytes within the immune system?
histamine
complement
bradykinin
cytokines
SLE all of the following are examples of hypersensitivity reactions except:
systemic lupus erythematosus
urticaria
angioedema
contact mucositis
an immunologic disorder reiter syndrome is:
Type IV which type of hypersensitivity reactions is referred to as delayed hypersensitivity?
erythema multiforme the "target lesions" on the skin is associated with which of the following diseases?
behect syndrome
SLE
lichen planus
erythema multiforme
pemphigus vulgaris tzanck cells are seen in which of the following conditions?
pemphigus vulgaris
erythema multiforme
SLE
behcet syndrome
geographic tongue the oral lesions in Reiter syndrome may resemble:
nicotine stomatitis
lichen planus
angioedema
geographic tongue
Langerhans cell disease aphthous ulcers are seen in each all of the following systemic disease EXCEPT:
behcet syndrome
Langerhans cell disease
ulcerative colitis
cyclic neutropenia
eosinophils and mononuclear cells the two cell types that histologically characterize Langerhans cell disease are:
Hand-Schuller-Christian disease which one of the foolowing is the form of Langerhans cell disease that is characterized by a triad of symptoms?
eosinophillic granuloma the most benign type of langerhans cell disease is:
xerostomia the most characteristic oral manifestation of Sjogren syndrome is:
skin lesions are common in mucous membrane pemphigoidwhich of the following statements is false?
- the bullae in pemphigus vulgaris are more fragile than those in bullous pemphigoid
- acantholysis of the epithelium is seen in pemphigus vulgaris
- in pemphigoid the separation of the epithelium from the CT occurs at the basement membrane
- skin lesions are common in mucous membrane pemphigoid
the histologic findings which is the most distinct and definitive characteristic that distinguishes pemphigus from pemphigoid?
all of the above desquamative gingivitis may be seen in:
cicatricial pemphigoid
pemphigus vulgaris
lichen planus
all of the above
epiglottis in angioedema involvement of which of the following tissues could create a life-threatening situation for the patient?
lips
mucosa
eyelids
epiglattis
lupus erythematosuswhich of the following is a pathologic condition that produces a characteristic butterfly-shaped lesion on the face and oral ulcers, occurs more frequently in women, and for which the result of a blood test is important to diagnosis?
pemphigus
erosive lichen planus
desquamative gingivitis
lupus erythematosus
angioedema
aphthous ulcer
aphthous ulcers
contact dermatitus
erythema multiforme
erythema multiforme
herpetiform aphthous ulcers
lichen planus
lichen planus
major aphthous ulcer
minor aphthous ulcers
mucous membrane pemphigoid
mucous membrane pemphigoid
pemphigoid vulgaris
pemphigoid vulgaris
pemphigoid vulgaris
raynaud's phenomenon
sjogren syndrome
SLE
urticaria
contact mucositis

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