Oral Manifestations of IBD Flashcards

1
Q

what is orofacial granulomatosis

A

persistent enlargement of soft tissues, characterised by non-caseating granulomatous inflammation in the absence of diagnosable crohns or sarcoidosis

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2
Q

prevalence and cause of OFG

A

0.8%
6-20% crohns with oral involvement

genetic + environment
mycobacterium?
deficiency, gut inflammation
delayed hypersensitivity reaction
triggers - benzoates, cinnamon, sorbate, SLS

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3
Q

describe the appearance of OFG

A

lip swelling, lymphoedema
lip fissures
peri-oral dermatitis
angular cheilitis
buccal cobblestoning
mucosal tags
gingival erythema
submandibular staghorning
ulceration
tongue swelling

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4
Q

describe the histological appearance of OFG

A
  • non-caseating granulomas +/- giant cells
  • granulomas deep in mucosa
  • lymphoedema
  • dilated lypmhatics
  • perivascular lymphatic infiltrate

indistinguishable from crohns

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5
Q

investigations for OFG

A

photos, differentiation
FBC, haematinics
inflammatory markers (ESR, CRP)
fecal calprotectin
deep biopsy
endoscopy/MRI if abdominal symptoms
serum ACE to exclude sarcoidosis
patch testing

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6
Q

management of OFG

A

exclusion diet of cinnamon, benzoate, sorbate 3 months, slow reintroduction

betamethasone 500mcg + 10ml water, rinse 5 mins, 5x
flixonase 400mct nasules
beclometasone 100mcg inhaler
clobetasol ointment 0.05%

lip swelling = intralesional triamcinolone 40mg/ml
liquid feeding if needed

systemic -
aza, mycophenolate, prednisolone

biologics -
for crohns, less so ofg
anti-tnf [infliximab, adalimimab]

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7
Q

name the varied types of diagnoses

A

OFG - absence of crohns or sarcoidosis

crohns with oral involvement

crohns alone

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8
Q

how does ulcerative colitis appear

A

pyostomatitis vegans

multiple pastels on erythematous base
labial/buccal mucosa, gingival, tonsillar
Aphthous ulcers, angular cheoliria, floristry

can erode to form snail track ulcer

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9
Q

what can happen with repeated episodes of OFG

A

baseline lip enlargement
= fibrosis

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10
Q

name granulomatous diseases in the head and neck region

A

OFG, sarcoidosis, granulomatous polyangitis, syphilis, tuberculosis, crohns

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11
Q

why is there lip oedema in OFG

A

chronic granulomatous inflammation, increased vascular permeability, lymphatic obstruction and fibrosis

compression of lymphatic vessels, impairs drainage and triggers swelling

inflammatory mediators TNF-alpha

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12
Q

Why is faecal calprotectin required for a child presenting with OFG

A

to assess for crohns disease
OFG may preceed

non invasive
elevated levels suggests occult GI inflammation

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13
Q

Explain why growth of a child needs to be monitored in OFG

A

possible underlying crohns - growth failure can be early sign

iron, folate,,b12 deficiencies
malnutritions

growth hormone resistance/interferences

delays of puberty

timely intervention

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14
Q

what is sarcoidosis

A

condition where the immune system overreacts, causing inflammation and the formation of granulomas (small, inflamed lumps) in various organs.

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15
Q
A
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