Allergies and Immunologic Disease Flashcards

1
Q

A common oral lesions involving fungiform or filiform papilla are called what?

A

Transient Lingual Papillitis

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2
Q

What are the 3 patterns of Transient Lingual Papillitis?

A

1-Localized
2-Generalized
3-Diffuse, papulokeratotic variant (like a callus version)

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3
Q

What is Recurrent Aphthous Ulcerations (RAU) also known as?

A

Recurrent aphthous stomatitis

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4
Q

In a normal patient, where do Recurrent Apthous ulcers occur?

A

Movable mucosa

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5
Q

What are the 3 clinical variations of Recurrent Apthous ulcers?

A

1-Minor (85%)
2-Major (10%)
3-Herpetiform (5%)

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6
Q

Which variation of Recurrent Apthous ulcers occurs in childhood on moveable mucosa and are 3-10 mm in size?

A

Minor

*heal in 7-14 days, no scarring, fewest recurrences

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7
Q

Which variation of Recurrent Apthous ulcers occurs in adolescents, are associated with suttons disease, and are 1-3 cm?

A

Major

*heal in 2-6 wks, possible scarring

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8
Q

Which variation of Recurrent Apthous ulcers occurs in adults, have up to 100 ulcerations, and are 1-3 mm mainly on moveable mucosa?

A

Hepetiform

*heal in 7-10 days, no scarring, most frequent recurrence

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9
Q

What is typically prescribed for recurrent aphthous ulcers?

A

topical corticosteroid (clobetasol proprionate)

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10
Q

Ocular inflammation, genital ulcers and skin lesions typically in Turkish, Japanese or eastern mediterraneans is called what?

A

Behcet’s Syndrome

*joint pain is also a common complaint

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11
Q

Which Multisystem granulomatous disorder of unknown cause happens more often in African americans, typically have an abnormal chest x-ray with skin lesions?

A

Sarcoidosis

*Involve lungs, lymph nodes, skin, eyes, salivary glands

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12
Q

What are the two types of skin lesions involved with sacradosis?

A

1-Lupus pernio (Chronic, purple, indurated lesions on H&N)
2-Erythema nodosum (Scattered, nonspecific, tender, red nodules on lower legs)

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13
Q

What are two different syndromes associated with sarcoidosis?

A

1-Lofgren’s syndrome

2-Heerfordt’s syndrome

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14
Q

What 3 things make up Lofgren’s syndrome?

A

1-Erythema nodosum
2-Bilateral hilar lymphadenopathy
3-Arthralgia

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15
Q

What 4 things make up Heerfordt’s syndrome?

A

1-Parotid enlargement
2-Inflammation of eye
3-Facial paralysis
4-Fever

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16
Q

What 3 things are used to diagnose Sarcoidosis?

A

1-Elevated serum angiotensin-converting enzyme levels
2-Chest XRAY
3-Kveim test – no longer used

17
Q

What condition most commonly involves the lips as non-tender persistent swelling?

A

Orofacial Granulomatosis

18
Q

What 3 things make up Melkersson-Rosenthal syndrome?

A

1-Cheilitis granulomatosa (swollen lip)
2-Facial paralysis
3-Fissured tongue

19
Q

What 3 things are typical of classic Wegener’s granulomatosis?

A

1-Necrotizing granulomatous lesions of respiratory tract
2-necrotizing glomerulonephritis
3-systemic vasculitis of small arteries and veins

20
Q

What oral lesion is a characteristic manifestation of Wegener’s Syndrome?

A

Strawberry gingivitis

21
Q

How is Wegner’s Syndrome diagnosed?

A

Indirect immunofluorescence detects presence of antineutrophil cytoplasm antibodies (ANCA)

22
Q

Which two types of Antineutrophil Cytoplasm Antibodies are detected for when diagnosing Wegener’s syndrome?

A

1-Perinuclear (p-ANCA)

2-Cytoplasmic (c-ANCA) (most useful)

23
Q

Large, red gingiva that may superficially slough due to flavoring is most likely what?

A

Contact Stomatitis from Cinnamon

24
Q

AKA Quincke’s disease, what condition is diffuse edematous swelling of the soft tissues with no pain, but itching and erythema may be present?

A

Angioedema

*Most commonly caused by histamine release from mast cell degranulation

25
Q

Angioedema with diffuse involvement of the head and neck is likely caused by what?

A

Angiotensin-converting enzyme (ACE) inhibitors such as the “prils” for Hypertension