Fibro-osseous Bone Disorders Flashcards

1
Q

What is Fibrous dysplasia?

A

Skeletal anomaly in which normal bone is replaced by poorly organised immature bone and fibrous tissue

Non-neoplastic

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2
Q

What age group is most affected by fibrous dysplasia?

A

Children & adolescents (as affects actively growing bone & progression ceases with age)

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3
Q

What is the cause of fibrous dysplasia?

A

Mutation in GNAS gene

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4
Q

What are the two classifications of fibrous dysplsia?

A

1) Monostotic (affects single bone) – More common
2) Polyostotic (multiple bones)

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5
Q

What is the presentation of fibrous dysplasia?

A

Asymmetrical, painless swelling – often in children & adolescents
May be associated with Albright syndrome

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6
Q

What are the most common sites of fibrous dysplasia?

A

Craniofacial bones (Maxilla > Mandible) & femur

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7
Q

What can be seen on this radiograph?

A

Fibrous dysplasia
Ill-defined border & loss of lamina dura
Early stage = More fibrous (radiolucent)

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8
Q

What are some histological features to look out for in fibrous dysplasia?

A

Islands of fibrous tissue embedded within bone
Immature woven bone with lack of osteoblasts

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9
Q

What are Ossifying/Cemento-ossifying Fibromas?

A

Benign, fibro-osseous NEOPLASM that affects jaws & craniofacial skeleton

(continue to enlarge, not self-limiting as with Fibrous Dysplasia)

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10
Q

What are the different pathological variants of ossifying/cemento-ossifying fibromas?

A

Cemento-Ossifying Fibroma (COF)
Juvenile Trabecular Ossifying Fibroma (JTOF)
Juvenile Psammomatoid Ossifying Fibroma (JPOF)

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11
Q

At what age groups do the different variants of ossifying/cemento-ossifying fibromas present?

A

Peak incidence in 3rd-4th decade (F>M 5:1) Cemento-Ossifying Fibroma (COF)

Children & Adolescents
Juvenile Trabecular Ossifying Fibroma (JTOF)
Juvenile Psammomatoid Ossifying Fibroma (JPOF)

NB: JTOF/JPOF multiple recurrence

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12
Q

Describe the expansion of lesions for ossifying/cemento-ossifying fibromas

A

Painless expansion of buccal & lingual plates of affected bone

Larger lesions: Expansion of lower border of mandible or maxillary antrum floor

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13
Q

Radiographically what would you see for a ossifying/cemento-ossifying fibroma?

A

Well-circumscribed & clearly demarcated lesion from surrounding normal bone*

Early lesions = Radiolucent
Later = Progressively more radiopaque

*distinguishing feature from Fibrous Dysplasia

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14
Q

Radiographically how can you distinguish between a cemento-ossifying fibroma and a cemento-blastoma?

A

No connection with roots of teeth for a cemento-ossifying fibroma

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15
Q

What is the managment for Ossifying/cemento-ossifying fibromas

A

Surgical excision

NB: JTOF/JPOF multiple recurrence

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16
Q

What is Cemento-osseous Dysplasia?

A

NON-Neoplastic, fibro-osseous condition affecting tooth-bearing regions (alveolar bone) of mandible & maxilla

17
Q

What are the different classifications of cemento-osseous dysplasia and what do they mean?

A

1) Periapical (typically anterior mandibular teeth)
2) Focal (single tooth)
3) Florid (multiple)
4) Familial Gigantiform Cementoma (genetic)

18
Q

Comment on the vitality of teeth affected by cemento-osseous dysplasia

A

Teeth remain vital

19
Q

What may you see radiographically for a cemento-osseous dysplasia lesion?

A

Well-circumscribed & surrounded by a thin radiolucent rim
Radiolucent, mixed or radiopaque – Increased density as lesions mature

20
Q

What is the managment for Focal Cemento-Ossifying dysplasia?

A

No tx & monitor

21
Q

What is the managment for Florid Cemento-Ossifying dysplasia?

A

Monitor closely (osteomyelitis complications)

22
Q

What is Paget’s disease?

A

Paget’s disease of bone disrupts the normal cycle of bone renewal, causing bones to become weakened and possibly deformed

23
Q

What genetic and environmental factors could potentially cause paget’s disease?

A

Genetic links = Chromosome 18q
Environmental links = Paramyxoviridae viral infection

24
Q

What age group is most affected by Pagets disease?

A

Patients over 40 years old

25
What are some manifestations of Pagets disease?
Susceptibility to fracture and deformity of weight bearing bones Cranial nerve disorders, deafness, vertigo and tinnitus occur as a consequence of nerve compression in foramina
26
What occurs during the Osteolytic stage of Pagets disease? | What may you also see on a radiograph?
Excessive bone resorption with replacement by fibrous and vascular tissue | Ill-defined radiolucent areas
27
What occurs during the Osteolytic and osteogenesis stage of Pagets disease? | What may you also see on a radiograph?
New bone formation within the fibrous tissue with simultaneous osteoclastic and osteoblastic activity | Mixed radiolucent and opacity on radiograph
28
What occurs during the Osteosclerosis stage of Pagets disease? | What may you also see on a radiograph?
Late phase in which the irregular haphazardly arranged bone coalesces to form dense sclerotic bone | The bone exhibits a dense radiopaque appearance
29
During the early stages of Pagets disease there is prominent resorption what are the dental implications of this?
Bone replaced by vascular stroma therefore there is an increased bleeding risk with XLA
30
During the late stages of Pagets disease there is prominent bone apposition what are the dental implications of this?
Irregular bone with minimal vascularity therefore there is an increased infection risk (Osteomyelitis)
31
Why may Pagets disease make extractions more difficult?
Hyper-cementosis which leads to bulbous roots which in turn leads to difficulty extracting
32
What medication will patients with Pagets disease be on?
Bisphosphontates
33
During the late stages of Pagets disease there is prominent bone apposition what are the dental implications of this?
Irregular bone with minimal vascularity therefore there is an increased infection risk (Osteomyelitis)