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21289485
Oro-facial Granulomatous Disorders
Description
First Year Dentistry Mind Map on Oro-facial Granulomatous Disorders, created by sanna pathy on 14/03/2020.
No tags specified
oral diseases
dentistry
first year
Mind Map by
sanna pathy
, updated more than 1 year ago
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Created by
Zainab Patel
almost 5 years ago
Copied by
sanna pathy
almost 5 years ago
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Resource summary
Oro-facial Granulomatous Disorders
Infectious
Tuberculosis
Types of infection
3) Secondary
Reactivation usually with reduced host defences
Oral (rare)
Ulcers or nodules on tongue or hard palate
single or multiple
Painful or Painless
Cervial LN & salivary gland swelling
1) Exposure to TB
Primary
Infection in lungs - formation of nodules
Oral (rare)
Tongue ulcers
95% asymptomatic
2) Bacteria latent
Diagnosis
Biopsy
Ziehl Niesson staining
Granulomas of TB with caseating necrosis
Mycobacterium tuberculosis
Droplet inhalation transmission
Tertiary Syphillis
Treponema pallidum
Sexually transmitted disease
Presentation
Rare - treated before this stage
Gummas = granulomatous lesions
Hard palate = common
Can perforate
can involve skin, CNS, liver
Earlier stages
Primary
Presentation
Chancre
= painless, indurated ulcer
At site of innoculation
Most comon = genitals
Can be on tongue, lip, palate
Resolves itself in 3-6wks
Highly infectious
Bilateral, painless lymphadenopathy
Secondary
Presentation
Most common = rash
Red/pink macules
Not itchy
Arms, flanks, palms & soles
Symmetrical
Can last wks-months
Other stages
Latent
Congenital
From pregnant mother to foetus
Effects
Still-birth, neonatal death
Hutchison's triad = notched incisors, deafness, ocular keratitis
Treatment = antibiotics
Diagnosis
DIF/PCR/microscopy
Serological tests
Actinomycosis
Rare, chronic
Actinomyces spp.
Forms
Cervicofacial = most common
Slow, progressive, indurated mass
Multiple abscesses & sinus tracts
Yellow, purulent discharge
Thoracic
Abdominal
Diagnosis
Histopathology
Cultures
Parasites
Non-infectious
Idiopathic OFG
= restricted to oral cavity with no known granulomatous disease
Crohn's disease
Clinical features
Oral
Angular cheilitis
Cobblestone mucosa
Aphthous-like oral ulcers
Stomatitis
Peripheral arthritis, erythema nodosum, pyogenic gangrenosum
Uveitis, Episcleritis
Diarrohea, weight loss, anaemia, abdominal pain
= Inflammatory bowel disease
Affects
Proximal colon
Terminal ileum
Melkerson's Rosenthal Syndrome
Clinical presentation
Fissured tongue
Facial paralysis
Facial swelling (lips)
Most common = lower lip
Rare for all to occur at the same time
Management
Elimination of diet
Topical Steroids
Weekly local injections of triamcinolone acetonide
Aetiology
Hypersensitivity
Foods
Dental materials
Infections
Mycobacteria
Cheilitis granulomatosa
Young adults
Clinical presentation
Recurrent, painless swelling of lips
Swelling becomes firmer with each recurrence
More common than complete triad
Wegener's granulomatosa
Clinical presentation
Systemic Vasculitis
Necrotic glomerulonephritis
Granulomatous lesions in respiratory tract
Strawberry gingivitis = Hyperplastic granular gingivitis
Hearing loss
Lung symptoms (cough, haemoptysis
Investigations
Chest X-ray
Biopsy
Sarcoidosis
Clinical presentation
Pulmonary issues
Skin
Erythema nodosum
Liver
Oro-facial
Bilateral parotid swelling
Soft tissue swelling
Investigations
Chest X-ray
Bat wing
Biopsy
High blood ACE levels
Young-middle aged women
Treatment
Corticosteroids
= multisystem granulomatous disorder with unknown cause
Foreign body reaction
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