RADIOLOGY - other pathologies Flashcards

1
Q

what factors contribute to lesions appearing radiopaque on radiographs?

A

increased thickness of bone
osteosclerosis of bone
presence of abnormal tissues
mineralisation of normally non-mineralised tissues

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2
Q

what are the 3 questions you ask yourself when you see an abnormality on a radiograph?

A

is it anatomical?
is it artefactual?
is it pathological?

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3
Q

when describing radiopaque and mixed lesions, what is the main deviation when comparing to radiolucencies?

A

its ‘internal structure’

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4
Q

what are the main categories when describing the internal structure of radiopaque and mixed lesions on imaging?

A

entirely radiopaque vs mixed (homogenous or heterogenous)
organised vs haphazard

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5
Q

what is an odontoma?

A

a dental hamartoma - benign tumour composed of dental tissues (enamel, dentine, cementum and pulp)

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6
Q

what similarities are there between normal teeth and odontomas seen on imaging?

A

surrounded by dental follicle
mature to a certain stage (i.e., do not grow indefinitely)

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7
Q

what is the incidence of odontomas?

A

1st or 2nd most common odontogenic tumour
most common in 2nd decade (correlates with development of normal dentition)
F=M

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8
Q

what are the sub types of odontomas?

A
  1. compound (ordered dental structures)
  2. complex (disorganised mass of dental tissue)
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9
Q

describe compound odontomas? and where would you find them?

A

may present as multiple ‘mini teeth’ (denticles)
more common in anterior maxilla

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10
Q

describe complex odontomas? and where would you find them?

A

may have a ‘clump of cotton’ appearance
more common in posterior body of mandible

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11
Q

what are radiographic features of odontomas?

A
  • well defined radiopacity/ radiopacities of varying radiodensity
  • areas with radiodensity of enamel
  • thin radiolucent margin i.e., follicle
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12
Q

what clinical issues do odontomas present?

A
  • impaction of adjacent teeth
  • external root resorption of adjacent teeth
  • development of dentigerous cyst
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13
Q

what is the management of odontomas?

A
  • excision if impeding eruption
  • no risk of recurrence
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14
Q

what is idiopathic osteosclerosis?

A

localised area of increased bone density of unknown cause
- no association with inflammatory, neoplastic or dysplastic processes

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15
Q

what area of dentistry is idiopathic osteosclerosis relevant to?

A

ortho

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16
Q

what are names for areas of idiopathic osteosclerosis?

A

‘dense bone island’
‘enostosis’

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17
Q

what is the incidence of idiopathic osteosclerosis?

A

up to 6% of the population
typically presents in adolescence and stops growing by adulthood
most common in premolar-molar region of mandible

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18
Q

describe the radiographic presentation of idiopathic osteosclerosis?

A
  • well-defined radiopacity
  • often homogenous but can have slightly radiolucent internal areas
  • no radiolucent margin
  • variable shape: round, elliptical, irregular
  • size usually <2cm
  • not associated with teeth but can appear next to them due to circumstance: teeth not displaced and no affect on the PDL spaces of teeth
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19
Q

what is sclerosing osteitis?

A

localised area of increased bone density in response to inflammation
- inflammation often low-grade and chronic

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20
Q

does sclerosing osteitis have symptoms?

A

may have concurrent symptoms due to source of inflammation
no expansion or displacement of adjacent structures

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21
Q

what is another name for sclerosing osteitis?

A

condensing osteitis

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22
Q

describe the radiographic presentation of sclerosing osteitis?

A

well defined or poorly defined radiopacity
directly associated with source of inflammation - apex of necrotic tooth, infected cyst etc

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23
Q

how can you differentiate sclerosing osteitis and idiopathic osteosclerosis?

A

if radiographic features inconclusive then look for a source of inflammation e.g., check for signs and symptoms, sensibility test teeth

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24
Q

what is hypercementosis?

A

excessive deposition of cementum around root

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25
Q

does hypercementosis have symptoms?

A

non-neoplastic and asymptomatic
tooth vital (unless necrotic due to another reason

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26
Q

what causes hypercementosis?

A

cause unknown but more common in certain conditions i.e., pagets disease of bone and acromegaly

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27
Q

what is the clinical relevance of hypercementosis?

A

makes xla more difficult

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28
Q

describe the radiographic presentation of hypercementosis?

A
  • single or multiple teeth involved - involves either entire root or just a section
  • homogenous radiopacity continuous with root surface - radiodensity subtly different to dentine of root
  • PDL space of tooth extends around periphery
  • margins often smooth but can be irregular
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29
Q

what is a cementoblastoma?

A

benign odontogenic tumour of cementum

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30
Q

where may you find cementoblastomas?

A

around root of a tooth (which remains vital)

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31
Q

what are the symptoms associated with cementoblastoma?

A

often painful
can displace adjacent teeth and cortical bone

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32
Q

what is the incidence of cementoblastoma?

A

rare
wide age range but often in 2nd and 3rd decades
typically affects mandibular premolars or 1st molars

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33
Q

describe the radiographic presentation of cementoblastoma?

A

attached to a tooth root - root outline may become indistinct
thin radiolucent margin continuous with PDL space of root
* no radiolucent margin separating tumour from root surface
well-defined and radiopaque - typically homogenous and round, can be mixed radiodensity and irregularly shaped

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34
Q

what are tori?

A

bony protuberances or normal bone at characteristic sites

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35
Q

where may you find tori?

A

middle of hard palate - torus palatinus
lingual to mandibular premolars - torus mandibularis

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36
Q

have tori got associated symptoms?

A

asymptomatic
may slowly increase in size

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37
Q

what is the cause of tori?

A

potentially related to genetic factors and masticatory stresses

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38
Q

what is the clinical relevance of tori?

A

can hamper denture wear
potentially traumatised during eating

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39
Q

what is the incidence of tori?

A

varies between populations
torus palatinus - 20% of population: often arise before age 30
torus mandibularis - 8% of population: often arise in middle age

40
Q

describe the radiographic presentation of tori?

A

solitary of multiple (torus mandibularis often bilateral)
cortical bone or a mix or cortical and trabecular bone
sessile or pedunculated
variable in size

41
Q

what is an osteoma?

A

benign tumour of bone
they can occur anywhere in body but have a predilection for craniofacial skeleton

42
Q

clinical presentation of osteoma?

A

hard, asymptomatic, slow-growing lump
single or multiple

43
Q

osteoma incidence?

A

rare
wide age range
posterior mandible is most common jaw site

44
Q

describe the radiographic presentation of osteoma?

A

entirely cortical bone or a mix of cortical and trabecullar
sessile or pedunculated
rounded, smooth margins

45
Q

what is the clinical relevance of osteoma?

A

no malignant potential
cosmetic or function issues (excise)
multiple osteomas may indicate gardeners syndrome

46
Q

what is gardener syndrome?

A

a rare variant of familial adenomatous polyposis

47
Q

what is gardener syndrome characterised by?

A

colorectal polyposis
osteomas (esp of mandible)
soft tissue tumours e.g., epidermoid cyst of skin

also tend to have supernumeraries, impacted teeth and multiple areas of idiopathic osteosclerosis

48
Q

why is it important for early diagnosis of gardener syndrome?

A

colorectal polyps inevitably become malignant
- mean age of cancer diagnosis (if not removed) if 39 years old

49
Q

what is the name of a rare genetic condition with various skeletal defects?

A

cleidocranial dysplasia

50
Q

what effect does cleidocranial dysplasia have on the teeth and jaws?

A
  • delayed eruption
  • multiple supernumerary teeth, leading to impaction of other teeth
  • multiple unerupted secondary teeth, due to multiple retained primary teeth
  • hypoplastic maxilla with high arched palate
  • increased prevalence of cleft palate
  • coarse trabecular pattern
51
Q

what effect does cleidocranial dysplasia have on the sinuses and rest of the body?

A
  • small maxillary sinuses
  • absent or partially formed clavicles
  • bossing (bulging) of the skull
  • hypertelorism (increased distance between orbits)
52
Q

what is osteomyelitis?

A

inflammation of bone and bone marrow due to bacterial infection

53
Q

what is osteoradionecrosis?

A

bone death resulting from irradiation
requires high energies of radiation (radiotherapy)

54
Q

what is MRONJ?

A

bone death associated with anti-resorptive or anti-angiogenic drugs

55
Q

what are radiographic features of osteomyelitis and osteonecrosis?

A

osteolysis + osteosclerosis: variable mixture of radiolucent and radiopaque areas
irregularities on inner/ outer aspects of cortical bone
sequestration of bone
periosteal bone reaction (primarily in osteomyelitis)
loss of lamina dura around teeth
pathological # of bone

56
Q

describe osteolysis?

A

breakdown of bone

57
Q

describe osteosclerosis?

A

thickening of bone

58
Q

name a reactive lesion with benign tumour-like behaviour?

A

central giant cell granuloma

59
Q

describe central giant cell granuloma?

A

slow growing lesion causing expansion of bone and displacement of teeth (minority of cases more aggressive and grow rapidly)

60
Q

central giant cell granuloma symptoms?

A

often asymptomatic but may be tender to palpation
may invade overlying soft tissue

61
Q

what is the incidence of central giant cell granuloma?

A

wide age range but majority before age 20
F>M
most commonly affects mandible anterior to molars

62
Q

what is the typical radiographic presentation of central giant cell granuloma?

A

site - mandible anterior to molars
size - any size
shape - unilocular or multilocular (when large) sometimes with internal thin septae
margins - well defined, poorly corticated, scalloped
internal structure - radiolucent
tooth involvement - no
effects - displacement of cortices; displacement of teeth; occasional external root resorption
number - single

63
Q

name the group of rare, benign, non-inheritable conditions where normal bone is replaced by connective tissue and abnormal bone?

A

fibro-osseous lesions

64
Q

what are the main types of fibro-osseous lesions?

A

cemento-osseous dysplasia (COD)
fibrous dysplasia (FD)
ossifying fibroma (OF)

65
Q

what type of fibro-osseous lesions can affect any part of the skeleton but have a predilection for the jaws?

A

fibrous dysplasia
ossifying fibroma

66
Q

what type of fibro-osseous lesions only affect the jaws?

A

cemento-osseous dysplasia

67
Q

how are fibro-osseous lesions diagnosed?

A

radiology

*histopathology can be unable to distinguish between different types

68
Q

why is accurate diagnosis of fibro-osseous lesions important?

A

prognosis and tx options vary greatly
inappropriate management increases the pt morbidity

69
Q

what are radiographic features to consider when diagnosing different types of fibro osseous lesions?

A

anatomical location
shape
size
pattern of matrix
margin (including zone of transition)

70
Q

what are the different forms of cemento-osseous dysplasia?

A

focal COD: single/ few localised lesions
periapical COD: lesions associated with apices of anterior mandibular teeth
florid COD: extensive lesion or many lesions

71
Q

what is the incidence of cemento-osseous dysplasia?

A

typically pts age 30-50 years
F»M
most common in Black ethnicities
mandible> maxilla

72
Q

clinical signs/ symptoms of cemento-osseous dysplasia?

A

often no signs/ symptoms
may be expansile (esp florid type)
rarely painful
can become infected: pain, suppuration

73
Q

radiological appearance of cemento-osseous dysplasia?

A

mixed-radiodensity lesions located at apices of vital teeth
- well defined radiolucency with varying amounts of well defined radiopaque material
- lamina dura lost
- PDL unaffected
- tooth displacement/ ERR is rare

74
Q

what does the appearance of cemento-osseous dysplasia depend on?

A

stage of the lesion maturation
(fully mature lesions can appear entirely radiopaque)

75
Q

what is the mx of cemento-osseous dysplasia?

A

usually no mx needed
removal if exposed by xla, mandibular atrophy or trauma

76
Q

what is the risk associated with intervening cemento-osseous dysplasia?

A

secondary infection
*avoid biopsy and xla of teeth involved

77
Q

why may you want to consider periodic radiographic review for cemento-osseous dysplasia?

A

to check for development of secondary solitary bone cysts

78
Q

what are the forms of fibrous dysplasia?

A

monostotic: single bone affected (most common)
polyostotic: multiple lesions affecting multiple bones
craniofacial: typically single lesions affecting multiple (fused) bones

79
Q

what is the incidence of fibrous dysplasia?

A

1:30000
mean age 25 years
F=M
favours posterior maxilla

80
Q

what is the clinical presentation of fibrous dysplasia in the jaw?

A

facial swelling due to bony expansion
may displace teeth
typically painless

81
Q

what is the radiological presentation of fibrous dysplasia in the jaw?

A

altered bone pattern
- highly variable: granular/ orange peel/ swirling/ wispy/ amorphous
- radiodensity increases as lesions matures

bone enlarges but maintains rough anatomical shape

margins indistinct and blend into adjacent bone
- broad zone of transition

82
Q

what is the mx of fibrous dysplasia?

A

no mx required if not causing functional/ aesthetic issues

if required; recontouring or radical resection

83
Q

explain the lifespan of fibrous dysplasia lesions?

A

they normally stop growing but may reactivate, typically after a precipitating event like pregnancy or jaw surgery

84
Q

name a fibro-osseous neoplasm occurring most often in tooth bearing areas?

A

ossifying fibroma

85
Q

where may you find ossifying fibroma?

A

majority occur in the mandible
rare cases in other craniofacial bones

86
Q

clinical presentation of ossifying fibroma?

A

slow growing bony swelling (however juvenile sub type can grow rapid)
often painless

87
Q

incidence of ossifying fibroma?

A

occurs at any age - mean age 31 years
F>M

88
Q

Radiographic presentation of ossifying fibroma?

A

rounded, expansile lesions - affected teeth displaced and may be resorbed
ranges from entirely radiolucent to completely radiopaque - radiodensity depends on stage of the lesion maturation
margins usually well defined
surrounding bone may be sclerotic

89
Q

what is the mx of ossifying fibroma?

A

removal indicated due to progressive growth
surgical enucleation or resection (usually enucleates in one piece)
12% recurrence rate

90
Q

name a chronic condition causing disordered remodeling of bone?

A

Pagets disease of bone

91
Q

what does pagets disease affect?

A

multiple bones at the same time - resulting in enlargement of bones, malocclusion, nerve impingement, and brittle bones
majority asymptomatic

92
Q

Pagets disease incidence?

A

up to 5% of patients >55 years
rare <40 years
M>F
more common in UK than other parts of the world

93
Q

what are radiographic features of Pagets disease of bone?

A

general enlargement of bones
abnormal bone pattern (cotton wool appearance)
osteolytic/ osteosclerotic patches of bone
radiodensity of altered areas linked to stage of disease
dental issues: migration. hypercementosis. loss of lamina dura

94
Q

what are the stages of Pagets disease of bone?

A

early/ osteolytic (more radiolucent)
intermediate/ mixed
late/ osteosclerotic

95
Q

what is osteoporosis?

A

decreased bone mass

96
Q

what causes osteoporosis?

A

age
secondary to nutritional deficiency, medications etc

97
Q

what are radiographic features of osteoporosis?

A

thinned cortices e.g., inferior border of mandible
sparse trabecular bone pattern - general radiolucent appearance
thinned lamina dura around teeth