theme 12 Flashcards

(34 cards)

1
Q

2 types of developmental bone lesions of mouth

A

torus palatinus

torus mandibularis

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2
Q

what is reactive exostosis

A

projection of bone caused by chronic trauma = periosteal irritation = bone deposition

remove surgically

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3
Q

what is an osteoma and what are the 3 causes

A

benign bony mass in jaw

developmental, reactive, benign neoplastic

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4
Q

2 clinical classifications for osteomaas

A

solitary or multiple

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5
Q

syndrome causing multiple osteomas and multiple odontomes

A

gardner syndrome

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6
Q

features of benign neoplasms of jaw

A

rare, slow growing, circumscribed,

overlap with odontogenic neoplasms clinically
mimic cysts on radiograph

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7
Q

what sort of carcinoma presents in jaw

A

metastatic carcinoma - metastasis of SCC

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8
Q

3 types of malignant neoplasms in jaw

A

metastatic carcinoma
marrow neoplasms
primary bone tumours - osteosarcoma, chondrosarcoma, mesenchymal chondrosarcoma

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9
Q

premalignant disease putting elderly patients at risk of osteosarcoma?

A

pagets

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10
Q

name for newly laid down bone by osteoblasts

A

osteoid

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11
Q

role of RANKL

A

ensure bony remodelling is balanced

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12
Q

2 types of giant cell lesions of jaw

A

giant cell granuloma - peripheral or central

hyperparathyroidism - produces lesions called brown tumour

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13
Q

characteristic of giant cell lesions

A

presence of osteoclasts

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14
Q

where does a peripheral giant cell granuloma present

A

gingiva only - friable + painless

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15
Q

where does a central giant cell granuloma present

A

involves underlying jaw bone

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16
Q

management of central giant cell granuloma

A
  1. curretage

2. injection of slow release steroids

17
Q

subtle change that takes place in oral cavity due to hyperparathyroidism

A

loss of lamina dura of interdental bone

18
Q

test to differentiation GCG and hyperparathyroidism

A

serum calcium elevated in hyper

19
Q

what is pagets disease

A

unregulated bone turnover

osteitis deformans

20
Q

complications of pagets disease

A

heart disease - bone normally helps shunt

pre-malignant to osteosarcoma

21
Q

symptoms of pagets

A
middle aged - elderly
slow onset
deafness, vision
facial distortion
numbness
skeletal symptoms 
oral - bone overgrowth, tooth spacing, bleeding after extractions, osteomyelitis, pain/numbness
22
Q

diagnosis of pagets

A
history
examination
radiographs - abnormal trabecular bone
alkaline phosphate levels elevated
bone biopsy - avoid as painful
23
Q

treatment of pagets

A

bisphophanates

denosumab

24
Q

4 types of fibro-osseous lesions

A

fibrous dysplasia
ossifying fibroma
cements-osseous dysplasia
cherubism

25
3 forms of fibrous dysplasia
monostotic - solitary multiple - in craniofacial bones polyostotic - throughout skeleton
26
mutation responsible for fibrous dysplasia
GNAS mutation
27
features of monostotic fibrous dysplasia
childhood onset, slow growth no tooth displacement - teeth grow through no systemic abnormality radiograph - diffuse edge, initially radiolucent then trabecular bone forms = ground glass
28
management of FD
self-limiting review until skeletal maturity cosmetic re-contouring denosumab - targeted therapy to with RANLK off
29
how to differentiate FD + ossifying fibroma
FD diffuse border, OF well circumscribed
30
features of ossifying fibroma
``` benign, slow growing mandible more common juvenile or adult ground glass radiolucenency well circumscribed progressive growth displaced adjacent structures ```
31
treatment of ossifying fibroma
surgical removal clear margins conservative removal
32
radiographic appearance of cementoosseous dysplasia
radiolucencies with radio-dense central areas (NIDUS)
33
what is cherubism
multilocular cystic lesions bilateral mandible + maxilla submandibular lymph nodes enlarged swelling at 3-4yrs, stable by 30
34
gene causing cherubism
autosomal dominant SH3BP2