random theme 5/6 Flashcards

1
Q

what is hairy tongue?

A

clinical manifestation of elongation of filiform papillae - no etiologic cause

asymptomatic

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2
Q

4 things hairy tongue is often a response to?

A

infection
fever
xerostomia
substances - antibiotics, tobacco

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3
Q

keratinolytic drug used for hairy tongue

A

podophydllin 25% in tincture of benzoin

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4
Q

what is geographic tongue

A

depapillation of the filiform papillae on the dorsal of the tongue causing erythmatosus configurations

often white border

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5
Q

microscopical signs of geographic tongue

A

loss of filiform papillae
elongated rete ridges
neutrophil accumulation in the superficial epithelium

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6
Q

what is median rhomboid glossitis?

A

rhomboidal or elliptical reddish smooth or nodular surface located in midline of tongue

often associated with candida

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7
Q

what are fordyce granules? how can they be removed?

A

manifestation of heterotic sebaceous glands

co2 laser therapy

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8
Q

what causes white sponge naevus?

A

mutation in keratin 13 or 4 - hyperkeratosis

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9
Q

features of white spongy naves?

A

asymptomatic, diffuse, bilateral, white lesions, shaggy/spongy/wrinkled surface

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10
Q

how to diagnose leukodema?

A

stretch buccal mucosa - opaque change will dissipate

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11
Q

difference between erosion + ulcerations

A

erosion - epithelium only

ulceration - whole epithelium breached

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12
Q

3 types of white oral lichen planus

A
  1. papular
  2. reticular
  3. plaque - like
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13
Q

when is lichen Planus most common + uncommon?

A

most common - posterior buccal mucosa

spread to tongue, gingiae, labial mucosa, vermillion of lower lip

uncommon - palate, FOM, upper lip

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14
Q

3 types of red oral lichen planus

A
  1. atrophic - erythematous
  2. erosive - ulcerative
  3. bullous - blisters
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15
Q

what is planopilaris?

A

Lichen Planus involving scalp + hair follicles

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16
Q

most common place to find lichen Planus skin lesions

A

volar wrists + forearms

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17
Q

what is lichen planus

A

chronic inflammatory disorder of stratified squamous epithelium

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18
Q

4 histopathological characteristic of lichen Planus

A
  1. hyperkeratosis
  2. civatte bodies - basal cell liquefaction with apoptic cells
  3. bank-like inflammatory infiltrate mainly composed of T cells
  4. absence of epithelia dysplasia
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19
Q

how to determine difference between LP + OLCL (oral lichenoid contact lesion)

A

cannot distinguish histologically

patch testing

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20
Q

what reaction can amalgam cause orally?

A

oral lichenoid contact lesion

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21
Q

which virus may cause oral lichen Planus?

A

HCV

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22
Q

2 features of OLP that cause increased risk of malignant transformation

A

reticular plaque

atrophic-erosive

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23
Q

5 special investigation in oral med

A
  1. blood test
  2. skin patch testing
  3. exfoliate cytology
  4. biopsy
  5. direct/indirect immunofluorescence
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24
Q

difference between direct + indirect immunofluroence

A

direct = detect in situ deposition of Ig and/or complements

indirect = detect circulating autoantibodies

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25
colour coding scheme for oral lesions
``` green = GDP monitor amber = GDP in conjunction with specialist unit red = specialist referral centre ```
26
description of smokers keratosis
lesion on palate with small red spots
27
what virus causes oral hairy leukoplakia
EBV
28
what is hydroxychloroquine sulphate used to treat?
oral lichen Planus
29
skin condition associated with geographic tongue?
psoriasis
30
characteristics of aphthous ulcers/stomatitis
``` superficial oral mucosa ulceratin recurrent no obvious cause usually self limiting individual healthy occur on non-keratinised oral ep usually ```
31
difference between major and minor recurrent aphthous stomatitis
minor = 1-5 ulcers, lasts 7-14 days, no scarring major = 1-2 ulcers, lasts >14 days, scar (deeper)§
32
what is herpetiform RAS
small ulcers merge to form irregular shaped larger ulcers >10 per crop lasts 7-21days +/- scarring
33
9 causes of RAS
1. genetics 2. haematinic deficiency 3. food allergy 4. gluten sensitivity 5. sex hormones 6. drugs - NSAIDs, B blockers, nicorandil 7. immunodeficiency 8. infections 9. trauma ulcers in systemic conditions too but not technically ras- behcets, reiters, cyclic neutropenia
34
deficiencies causing RAS
iron, folic, zinc, B1, B2, B6, B12
35
what is behcets disease?
recurrent oral ulceration with 2 of the following: recurrent genital ulcers, eye lesions, skin lesions, positive pathergy test
36
1st line of treatment for oral ulcers
topical corticosteroids
37
pemphigus lesions are threatening to what?
life
38
pemphigoid lesions are threatening to what?
sight
39
what causes pemphigus ?
anti-epithelial auto-antibodies against surface of the keratinocytes
40
characteristics of pemphigus
1. blisters + ulcerations 2. acantholysis 3. intra-epithelial 4. autoantibodies 5. intracellular deposits of IgG + c3 in immunofluorescence
41
2 types of oral pemphigus
pemphigus vulgaris | pemphigus paraneoplastic
42
most common oral pemphigoid
mucous membrane pemphigoid (MMP)
43
process of diagnosising bullis disease
1. history 2. clinical evaluation 3. direct immunofluorescence 4. indirect IF, immunoprecepitation, ELISA 5. diagnosis
44
what cell type is predominant in chronic inflammation/ granulomatosis
activated macrophages
45
4 clinical manifestations of orofacial granulomatosis
1. erythema 2. ulceration 3. oedema 4. tissue enlargement
46
3 types of infection granulomatous disorders
1. TB 2. tertiary syphilis - gumma 3. mycotic granulomatous infection
47
bowel condition causing orofaical granulomatosis
crohns disease
48
triad for diagnosis of melkersson-rosenthal syndrome?
persistent orofacial swelling fissured tongue facial paralysis
49
7 causes of non-infectious orofacial granulomatosis
1. idiopathic OFG 2. crohns 3. melkerson-rosenthal syndrome 4. cheilitis granulomatosis of miescher 5. sarcoidosis 6. wegeners granulomatosis 7. foreign body reaction
50
what is chelitis granulomatosa
painless enlargement of 1/both lips - recurrent
51
triad to diagnose wegeners granulomatosis
1. necrotising granulomatous lesions upper/lower respiratory tract 2. systemic vasculitis 3. necrotising glomulonephritis
52
what is sarcoidosis
multisystem granulomatous disorder of unknown cause
53
what is orofacial granulomatosis
persistent enlargement of face/oral cavity | caused by inflammation
54
orofacal manifestations of granulomatosis
soft tissue swellings major salivary gland enlargement - mainly parotid ulcerations
55
bacteria causing TB
mycobacterium tuberculosis/tb bacilli
56
staining test for TB
ziehl Neelson
57
colour of amalgam tattoo
grey-blue
58
histology of malanotic macule
increased melanin pigmentation in basal cell layer | no increase in melanin number
59
how to tell difference between freckle + melanotic macules
``` freckle = worse with sun melanotic = no change with sun ```
60
what is naevi
mole - proliferation of melanocytes
61
how would you treat oral naevi
excision - may be melanoma
62
what is melanoma
aggressive tumour of melanocytes
63
where are melanomas mostly found
hard palate, gingiva, tongue
64
clinical appearance of melanomas
pigmented plaques with asymmetrical irregular borders dark brown/black (5-15% amelanotic/pink) rapidly enlarging nodes causing - ulcers, bleeding, pain, tooth mobility normally metastic not primary
65
2 types of oral melanomas
radial growth phase - in situ | vertical growth phase - invasive
66
clinical appearance of smokers melanosis
patchy brown macular pigmentations - buccal mucosa
67
histology of smokers melanosis
basilar melanosis without melanocyte proliferation
68
oral manifestation of peutz-jehgers syndrome
lips + buccal mucosa pigmentation GI involvement too
69
most common drug induced pigmentation
minocycline induced pigmentation
70
6 options for peripheral diagnosis of soft tissue lump
``` cyst abscess granuloma hyperplasia neoplasia benign neoplasia malignant ```
71
6 examples of hyper plastic soft tissue lumps
``` fibroepithelial polylp pyogenic granuloma epulides denture granuloma squamous cell papilloma mucoceles ```
72
what is an epulis
any swelling on gingiva | development or reactive (calculus, partial)
73
When to treat OLP
if erosive or symptomatic
74
treatment options for OLP
1. high potency topical steroids 2. systemic steroids or ciclosporin if SS contradicated SS +/- azathiopine
75
treatment order of minor RAS
1. chlorhexidine mouthwash 2. topical steroids 3. systemic steroids
76
treatment of major RAS
1. topical steroids | 2. systemic steroids
77
treatment of herpetiform
systemic steroids | then topical
78
treatment for MMP or PV
topical or systemic steroids with adjunct agents or other immunosuppressants if contraindicated