Allergies/Immunologic Flashcards

1
Q

_ aphthae (recurrent aphthous stomatitis)- 3mm ulcer with yellow-white membrane and erythematous halo; unattached mucosa

A

minor

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2
Q

_ aphthae (recurrent aphthous stomatitis) - larger (up to 3cm) and longer duration (2-6 weeks); may heal with scar; HIV

A

major

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3
Q

_ aphthae- numerous, small lesions; predominantly non-keratinized mucusa

A

herpetiform

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4
Q

Combination of oral aphthous-like ulcerations, and ocular inflammation (anterior and posterior uveitis); probably an immunogenic process with a strong association to certain HLA types

A

Behcet’s Syndrome

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5
Q

Oral ulcerations of _: aphthous-like ulcerations located primarily on soft palate and oropharynx

A

Behcet’s Syndrome

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6
Q

cutaneous lesions of _: erythema nodosum, papulopustular lesions, acneform lesions

A

Behcet’s syndrome

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7
Q

Behcet’s syndrome- histo similar to aphthous with leukocytoclastic vasculitis

A

Behcet’s

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8
Q

F>M, blacks>whites, typically occurs during the 3rd and 4th decades; dyspnea, dry cough; fever, malaise; fatigue, arthralgia; lymphadenopathy

A

sarcoidosis

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9
Q

skin lesions of _: lupus pernio and erythema nodosum

A

sarcoidosis

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10
Q

_ of sarcoidosis: parotid enlargement, anterior uveitis, facial paralysis, fever

A

Heerfordt’s syndrome

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11
Q

_ of sarcoidosis: arthralgia, bilateral hilar lymphadenopathy, erythema nodosum

A

lofgren’s syndrome

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12
Q

_ of sarcoidosis: langhans’ or foreign body giant cells; schaumann bodies; asteroid bodies

A

granulomatous inflammation

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13
Q

Highly variable presentation; involvement of lips- cheilitis granulomatosa

A

orofacial granulomatosis

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14
Q

_ of orofacial granulomatosis: non-tender swelling, usually involving lips; Bell’s palsy; fissured tongue

A

Melkersson-Rosenthal syndrome

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15
Q

_ granulomas may be sparse in orofacial granulomatosis

A

non-necrotizing

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16
Q

Necrotizing granulomatous process; classically affects upper airway, lungs, kidneys; epistaxis, pain, nasal obstruction

A

Wegener’s granulomatosis

17
Q

multisystemic vasculitis of small arteries and veins; occasionally involves the eyes, ears and skin

A

wegener’s

18
Q

oral lesions of _: large, chronic ulcers and “strawberry gums”

A

wegener’s

19
Q

may present with systemic signs or symptoms; multiple ones of erythema or aphthous-like eruptions

A

anaphylactic stomatitis

20
Q

localized erythema and edema; vesiculoerosive lesions

A

fixed drug reaction

21
Q

_ allergic contact stomatitis- burning, erythema, occasional vesicles

A

acute

22
Q

_ allergic contact stomatitis- erythematous or white, may extend beyond the oral cavity

A

chronic

23
Q

_ reaction more generalized (stomatitis from artificial cinnamon): pain, burning, erythema; frequently will affect the gingiva; may extend to perioral tissue

A

toothpaste

24
Q

_ (cinnamon flavoring) often localized to the buccal mucosa or lateral borders of the tongue: ragged hyperkeratosis; erythematous base

A

gum, candy

25
Q

chronic reactions resemble localized lichen planus-like lesions

A

chronic (lichenoid) oral mucosal contact reactions to dental amalgam

26
Q

posterior buccal mucosa or lateral surfaces of the tongue; white and/or erythematous, often with peripheral striae

A

contact reactions to amalgam

27
Q

3 primary mechanisms of _: hypersensitivity rxn due to IgE mediated mast cell degranulation; associated with ACE inhibitors, secondary to increased bradykinin levels; lack of or inactive C1 esterase inhibitor (inherited or acquired)

A

angioedema (Quincke’s disease)

28
Q

enlargement of relatively rapid onset; pruritis, erythema; respiratory involvement may be life threatening

A

angioedema

29
Q

angioedema: _ and _ don’t respond to antihistamines

A

ACE inhibitor related and C1-INH deficient