Allergies and immunologic Diseases Flashcards

(51 cards)

1
Q

canker sores
familial relationship,
unknown pathogenesis; immune mediated process
most common in children and young adults

A

recurrent aphtous ulcerations

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2
Q

what are the 3 clinical variations of recurrent aphthous ulcerations?

A

minor
major
herpetiform

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3
Q

most common recurrent aphthous ulcerations

A

minor aphthous ulcerations

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4
Q

most common form
only on NONKERATINIZED MUCOSA
most common sites are buccal and labial mucosa ventral tongue, floor of mouth and soft palate
1-5 PAINFUL ulcers preceded by erythematous macule and prodromal symptoms
ERYTHEMATOUS HALO

A

minor aphthous

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5
Q

which one of the aphthous ulcerations heal without scaring?

A

minor

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6
Q

3-10 mm diameter -
1-3 cm diameter-
1-3 mm diameter -

A

minor
major
herpetic

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7
Q

1-5 PAINFUL ULCER -
1-10 lesions per episode
many present per episode

A

minor
major
herpetic

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8
Q

heal in 7-14 days
heal in 2-6 weeks
heal in 7-10 days

A

minor
major
herpetic

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9
Q

buccal and labial mucosa, ventral tongue, floor of the mouth, soft palate

labial mucosa, soft palate, tonsillar fauces

any oral mucosal surface

A

minor

major

herpetic

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10
Q

true or false

minor aphthous does not cross the MGJ

A

true

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11
Q

true or false

major aphthous has lesser erythmatous halo compared to minor

A

true

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12
Q

which of the the following has resemblance to primary HSV?
minor
major
herpetiform

A

Herpetiform

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13
Q

which of the following has most frequent recurrences?
minor
major
herpetiform

A

herpetiform

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14
Q

what is the medication for Recurrent Aphthous Ulcerations?

A

topical HIGH-potency corticosteroids

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15
Q

multisystem disorder with oral aphthous like ulcerations
affects genetically predisposed individual
Highest prevalence in Turkey, Japan and Eastern mediterranean countries

A

Behcet’s syndrome

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16
Q

what is the triad for behcet’s syndrome

A

oral ulcerations
genital ulcerations
ocular disease

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17
Q

which of the following has cutaneous leisions, arthritis, CNS involvement, cardiovascular, GI, pulmonary, renal?

oral
genital
ocular

A

ocular disease of the behcet’s syndrome

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18
Q

posterior uveitis

A

ocular

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19
Q

you have a positive pathergy test. what is the diagnosis?

A

behcet’s syndrome

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20
Q

what is the treatment for behcet’s syndrome?

A

topical or systemic immunosuprressive therapy

early aggressive therapy for severe cases

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21
Q

non-necrotizing granulomatous inflammation,
persistent non-tender swelling
LIPS most common site, may involve any oral mucosal or perioral location

A

orofacial ganulomatosis

22
Q

what are the two forms of orofacial granulomatosis?

A

cheilitis granulomatosa

melkersson-rosenthal syndrome

23
Q

which of the two orofacial granulomatosis have only lips involvement

A

chelitits granulomatosa

24
Q

A person has bell’s palsy, fissured tongue, non-tender lip swelling.
non-necrotizing granulomatous inflammation

A

melkerssson-rosenthal syndrome (one of the two orofacial granulomatosis

25
what are the microscopic features of orofacial granulomatosis?
superfical vascular ectasia, vasculitis, edema non-necrotizing granulomas no evidence of foreign material and specific stains to rule out specific infection
26
medication for orofacial granulomatosis
intralesional corticosteroids work best | multiple injections may be necessary
27
necrotizing granulomatous process with vasculitis can affect upper airway, lungs, kidneys, skin and mucosa wide range of age group
wegener's granulomatosis
28
what are the 3 categories of wegener's granulomatosis
1. Generalized wegener's 2. limited 3. superficial
29
generalized wegeners
upper and lower respiratory tract, kidneys
30
limited wegener's
upper and lower respiratory tract
31
superficial wegener's
lesions primarily of skin and mucosa
32
STRAWBERRY GINGIVITIS - panthognomonic | this is very specific to this condition
wegener's granulomatosis
33
destruction of nasal septum (saddle-nose deformity) dry cough, hemoptysis, dyspea, chest pain proteinuria, palatal ulcer with oral-antral fistula
wegnener's granulomatosis
34
what is the microscopic appearance of wegener's granulomatosis?
subepithelial hemorrhage, vasculitis poorly formed granulomas, mixed inflammation
35
autoantibodies directed against neutrophils have been identified in high percentage of these patients (ANCA)
wegener's
36
what is the prognosis of wegener's granulomatosis
complete response in 75% relapse in 30% prednisone and cyclophosphamide vs methotrexate
37
what are the two types of allergic reaction to systemic drugs?
fixed drug eruption | lichenoid drug reaction
38
fixed drug eruption?
inflmaatory alteration that recur at the same site after the administration of a medication
39
lichenoid drug reaction
medicaiton induced mucosal alterations which mimic appearche of lichen planus which is white line or stria
40
what are there 3 allergic contact stomatitis?
1. dentrifice-related sloughing 2. orla mucosal cinnamon reaction 3. lichenoid amalgam reaction
41
what is associated with sodium lauryl sulfate and sodium pyrophophate? found in toothpastes
dentrifice-related sloughing
42
clinical varation of oral mucosal cinnamon reaction toothpaste: chewing gum/candy:
diffuse, gingiva localized
43
patient has erythema with overlying SHAGGY HYPERKERATOSIS, | pain and buring
oral mucosal cinnamon reaciton
44
how long does it take to resolve oral mucosal cinnamon reaction
1 week following discontinuation of the cinnamon product
45
lichenoid amalgam reaction
associated with old amalgam restorations undergoin corrosion and release of metallic ions mucosal alterations mimic lichen planus HOWEVER are LOCALIZED. may be white or erythematous
46
what is the differential diagnosis of lichenoid amalgam reaction?
true leukoplakia would the differential diagnosis. | key is to look if the amalgam is contacting the mucosa
47
will smith reaction in mr. hitch
angioedema
48
IgE mediated hypersensitivity reaction
angioedema
49
NON-PAINFUL pruritus and erythema may be seen solitary or multiple sites may be involved relatively rapid onset of sof ttissue swelking
Angioedema
50
what inhibitor is involved in angioedema?
C1 esterase inhibitor and | ACE inhibitor
51
excess bradykin
angioedema