Ch. 9 Allergy/Immunologic, Part 1 Flashcards

1
Q

Transient lingual papillitis other names

A

bumps, tongue torches

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2
Q

Local irritation, inflammation, hormones, stress, hypersensitivity cause a reaction of the ______ papillae in transient lingual papillitis

A

fungiform

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3
Q

3 clinical patterns of transient lingual papilitis

A

Localized
Generalized
Papulokeratotic

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4
Q

Most common location for localized transient lingual papillitis, the condition usually lasts for _____

A

anterior dorsal tongue

hours to days

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5
Q

Causative agent for:
localized TLP
generalized TLP

A

localized: maybe a food allergy
generalized: maybe viral as it is passed around families

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6
Q

Large % of the fungiform papillae located on the ______ tongue are affected in generalized TLP

A

tip and lateral dorsal

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7
Q

T/F papillae involved by papulokeratotic variant of TLP are symptomatic

A

false- asymptomatic

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8
Q

What causes the white appearance of the papulokeratotic variant of TLP

A

thickened parakeratotic cap

bacterial colonization

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9
Q

On average ____% of the population are affected by recurrent aphthous stomatitis

A

20%

ranges from 5-66%

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10
Q

Systemic disorders associated with recurrent aphthous stomatitis (11)

A
Behcet syndrome
IgA deficiency
Celiac disease
Cyclic neutropenia
Nutritional deficiencies
IBD
HIV and other immunocompromised
Reactive arthritis
-Sweet syndrome: very rare inflammatory skin condition characterized by a sudden onset of fever and painful rash on the arms, legs, trunk, face, or neck.
-MAGIC syndrome: mouth and genital ulcers with inflamed cartilage
-PFAPA syndrome: periodic fever, aphthous stomatitis, pharyngitis, cervical adenitis 
Ulcus vulvae acutum
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11
Q

____% of patients with recurrent aphthous stomatitis have some underlying condition

A

60%

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12
Q

3 clinical variants of aphthous stomatitis and their alternative names

A
Minor aphthous (Mikulicz aphthae)
Major aphthous (Sutton disease)
Herpetiform aphthae
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13
Q

what % of aphthae are each type

A

80% minor
10% major
10% herpetiform

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14
Q

which type of aphthae are typically adult onset

A

herpetiform type

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15
Q

Simple vs complex aphthosis

A

Simple aphthosis: few lesions, heal in 1-2 weeks, recur infrequently
Complex aphthosis: 3 or more lesions, almost constant overlapping bouts of lesions; severe pain and large size are frequent

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16
Q

Behcet syndrome alternate names

A

Behcet disease, Adamantiades syndrome

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17
Q

classic triad of behcet syndrome

A

oral, genital and ocular inflammation

now we include systemic vasculitis

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18
Q

What genetic variation is associated with increased risk of Behcet syndrome

A

HLA-B51

frequent in japan, turkey, and eastern mediterranean

19
Q

demographics of behcets

A

slight male predominance

3rd-4th decades

20
Q

almost all behcet patients have oral ulcers. Most commonly what type?

A

Minor, but up to 40% have major type, and only 3% have herpetiform type

21
Q

What % of behcet syndrome patients have genital ulcers?

A

75%

deep ulcers that tend to scar

22
Q

T/F Blindness occurs in 25% of patients with ocular involvement of behcet disease

A

True

23
Q

What % of patients with behcet disease have CNS involvement

A

10-25%

poor prognosis

24
Q

International study group criteria for diagnosis of Behcet disease (no lab criteria)

A

Major criteria: oral aphthae

(2) Minor criteria: recurrent genital ulcers, eye lesions, skin lesions, positive pathergy test

25
Q

What is a positive pathergy test? What is it used to diagnose

A

Stick a sterile 20 gauge needle into the skin, inject saline
One to two days later a sterile papule arises
*occurs in 60% of mediterranean behcets patients but only 3% of caucasians
- used to aid in the diagnosis of Behcets

26
Q

what histologic pattern is seen in behcets ulcerations

A

leukocytoclastic vasculitis

Vessels show: intramural invasion by neutrophils, karyorrhexis(destructive fragmentation of the nucleus) of neutrophils, extravasation of red blood cells, and fibrinoid necrosis of the vessel wall

27
Q

Demographics for sarcoidosis

A

black, female, before age 50

28
Q

what % of patients with sarcoid are asymptomatic at diagnosis

A

20%

29
Q

Predominant sites affected by sarcoidosis

A

lungs, lymph nodes, salivary glands, skin and eyes

*Mediastinal and paratracheal lymph nodes

30
Q

What is a common radiographic sign of sarcoid of chest xray

A

bilateral hilar LAD

31
Q

what are the indurated skin lesions of the nose,ears,lips and face in sarcoid?

A

lupus pernio

  • Occurs in 25% of patients
  • Frequent in head and neck region
32
Q

What is a non-specific skin lesion often on the lower leg in sarcoidosis?

A

erythema nodosum

33
Q

If sarcoidosis affects the lacrimal gland what condition can it mimic

A

keratoconjunctivitis sicca of sjogrens syndrome

34
Q

What are the two clinical syndromes of Acute sarcoidosis

A
  1. Lofgren syndrome

2. Heerfordt syndrome

35
Q

Features of Lofgren syndrome

A
  1. erythema nodosum
  2. bilateral hilar LAD
  3. arthralgia
36
Q

Features of Heerfordt syndrome aka uveoparotid fever

A
  1. parotid enlargement
  2. anterior uveitis
  3. facial paralysis (ON THE BELLS PALSY DIFFERENTIAL)
  4. fever
37
Q

In what % of patients are oral manifestations the first sign of sarcoidosis

A

2/3 66%

38
Q

Are there intraosseous lesions of sarcoid?

A

yes- 1/4 of patients

39
Q

3 Histologic buzzwords for sarcoid

A
  • tight epithelioid GRANULOMAS
  • Schaumann bodies: laminated basophilic calcifications within the granulomas
  • Asteroid bodies: entrapped collagen within the granuloma
40
Q

serum marker that can be elevated in sarcoidosis

A

60% of patients have elevated ACE

41
Q

What WAS the skin test for sarcoid?

A

Kveim test (intradermal injection of sterilized suspension of sarcoid tissue)….Not done anymore

42
Q

Helpful diagnostic aid which leads to diagnosis in 93% of patients

A

parotid biopsy

43
Q

What % of patients have spontaneous resolution of sarcoidosis in 2 years

A

60%….10-20% of patients do not get resolution even with treatment…4-10% die of cardiac, respiratory, or CNS complications

44
Q

Ocular involvment in sarcoid: 25% of the time and what is the clinical term (presentation)?

A

anterior uveitis