Malignant Bone Tumors Of The Jaw Flashcards

1
Q

Benign bone tumors

A

Osteoblastoma
Osteoma
Osteochondroma

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2
Q

Malignant bone tumor

A

Osteosarcoma
Chondrosarcoma

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3
Q

Signs and symptoms of malignancy in the jaw

A

Paresthesia
Pain
Tooth mobility
Tooth resorption
Rapid growth
Acquired malocclusion
Radiographic changes
Uniformly widened PD membrane space
Ill-defined lesion

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4
Q

Unilateral coronoid hyperplasia

A

Osteochondroma

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5
Q

Benign neoplasm forming a bony projection with a cartilagenous cap, with continuity between the marrow cavity of the tumor and underlying bone

A

Osteochondroma

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6
Q

Painless, facial asymmetry, trismus, TMJ dysfunction

A

Osteochondroma

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7
Q

Localization: coronoid process, mandibular condyle

Onset at puberty

A

Osteochondroma

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8
Q

Benign cartilagenous tumor of unknown cause. Rarely seen

Appears as painless, slowly progressive swelling

A

Chondroma

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9
Q

Chondroma that airses in the maxillary region usually found in?

A

Anterior region, where cartilaginous remnants of development are located

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10
Q

Location of mandibular chondromas

A

Body and symphysis area. Coronoid process and condyle

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11
Q

Equal gender predilection

Majority of tumors appear before age of 50

A

Chondroma

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12
Q

Irregular radiolucent. Foci of calcification within the radiolucent lesion

A

Chondroma

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13
Q

__ pharyngeal arch does meckel’s cartilage originate

A

First

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14
Q

A cartilage that forms in the embryonic development of lower jaw

A

Meckel’s cartilage

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15
Q

Well defined lobules of mature hyaline cartilage

Contains single regular nuclei

A

Chondroma

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16
Q

exhibits a heterogeneous pattern with cytologically
atypical and irregularly spaced chondrocytes.

A

Chondrosaroma

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17
Q

Treatment of chondroma

A

Surgical excision

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18
Q

3rd most common bone malignancy after myeloma and osteosarcoma

A

Chondrosarcoma

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19
Q

30 - 60 yo with 75% in men.

1% occur in skeleton

A

Chondrosarcoma

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20
Q

60% occur in maxillofacial region and 40% in mandible

A

Chondrosarcoma

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21
Q

Mandibular chondrosarcoma occus most often in

A

Premolar and molar region

Symphysis and coronoid process

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22
Q

Maxillary chondrosarcoma occurs in

A

Lateral incisor - canine region

Palate

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23
Q

No gender predilection

60yo

A

Chondrosarcoma

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24
Q

Common signs: painless swelling, bone expansion - loosening of teeth or dentures, pain, visual disturbances, nasal signs and headache

A

Chondrosarcoma

25
Moth-eaten radiolucencies that are solitary or multilocular to diffusely opaque lesions Localized widening of the PDL space
Chondrosarcoma
26
Preferred method to image chondrosarcoma
computed tomography
27
DD of chondrosarcoma
Chondroma Chondroblastic variant of osteosarcoma Chondromyxoid fibroma
28
Have a lobular achitecture Increased number if chondrocytes
Grade 1 - well differentiated chondrosarcoma
29
Enlarged chondrocyte nuclei displaying occasional mitotic figures. Increased cellularity at the periphery of the cartilaginous lobules
Grade 2 - intermediate chondrosarcoma
30
Markedly cellular, often with a spindle cell component. Mitotic figures may be numerous
Grade 3 - poorly differentiated
31
5 year Survival rate and metastasis in chondrosarcoma
GRADE 1 - 78%; 4% GRADE 2 - 53%; 10% GRADE 3 - 22%; 70% - metastasis in lungs
32
Most common primary bone tumor (5%)
Osteosarcoma
33
Exits in other bone disease: paget’s disease, fibrous dysplasia, multiple osteochondromas, osteomyelitis, osteogenesis imperfecta 3-4 onset of symptoms prior to diagnosis
Osteosarcoma
34
Etiology of osteosarcoma Gene that may be altered -
p53 Rb Amet fos sas mdm2 cdk4 c-myc
35
Swelling, pain, pdl invasian, tooth mobility 35 age: range from 8 to 85yo = gender predilection 60 % Mandible > maxilla
Osteosarcoma
36
Osteosarcoma can a,so arise in two cancer susceptibility syndromes __ and __ They sre both inherited and acquired forms of Rb
Hereditaryvretinoblastoma (Rb) and Li-Fraumeni syndrome
37
Comon site of osteosarcoma
Body and angle of mandible, symphysis, ascending ramus, tmj
38
Cardinal sign of malignancy
Paresthesia, caused by compression or infiltration of adjacent nerves by tumor
39
Radiographically, early osteosarcoma shows what characteristics?
Localized swelling in pdl of one or two teeth (due to tumor invasion)
40
Histologic subtype: when malignant cartilage predominates
Chondroblastic osteosarcoma
41
Histologic subtype: when malignant bone and osteoid predominates
Osteoblastic osteosarcoma
42
Histologic subtype: when spindle cells predominate
Fibroblastic osteosarcoma
43
Rare variant, that microscopically, resembles fibrous dysplasia because of the minimally atypical spindle cell proliferation with occasional mitotic figures and bone spicules
Central low-grade osteosarcoma
44
A useful immunohistochemistry marker to identify low grade osteosarcoma
CDK4 AND MDM2
45
Is CDK4 and MDM2 positive in high grade osteosarcoma?
No
46
Most common subtype of osteosarcoma
Chondrobastic osteosarcoma (Maybe misdiagnosed as chondrosarcoma)
47
Treatment of osteosarcoma
Radical surgery, chemo and radio
48
Osteosarcoma that arise at the periphery of bone at the periosteal surface Uncommon neoplasm
Juxtacortical osteosarcoma
49
Peak incidence 39 yo Most common: distal femoral, metaphysis 3:2 female predominance. If jaw, male
Parosteal osteosarcoma
50
long-standing, slow-growing, swelling or palpable mass, often accompanied by a dull, aching sensation Attached to the external surface of bone by a broad sessile base Radiopaque at the base than the periphery
Parosteal osteosarcoma
51
20 yo peak incidence 2:1 male Involve upper tibial metaphysis Very rare
Periosteal osteosarcoma
52
Codman’s triangle
Periosteal osteosarcoma
53
Consistent imagine features, tumor cells producing immature osteod premative invasion, entrapment of healthy host bone
Osteosarcoma
54
Malignant tumor with cartilaginous matrix, entrapped pre-existing bone, lack of neoplastic bone or osteoid formation
Chondrosarcoma
55
Soft tissue mass composed off nodules of cartilage, hyaline or myxoid matrix that may calcify, few mitosis
Chondroma
56
Pedunculated eor broad-based exostosis, cartilaginous cap with a growth plate-like architecture, continuity with underlying bone cortex and marrow
Osteochondroma
57
Osteobladtic riming
Ossifying fibroma Osteoblastoma
58
Associated with gardner syndrome
Osteoma