Path Chapter 3
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99 terms
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 ulcer | E: 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 pathogenesisL: 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 pathogenesisL: 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 vesselsL: 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 mucosaL: 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 skinL: 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 eruptions | E: 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 multiforme | E: 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 planus | E: 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 flowL: 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 Vulgaris | E: 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 diseasea/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 diseasea/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 pemphigoid | which 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 erythematosus | which 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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