nonneoplastic diseases of bone ch. 8 quiz 4 Flashcards

(41 cards)

1
Q

what are the benign fibro-osseous lesions

A

periapical cemento-osseous dysplasia
focal cemento-osseous dysplasia
florid cemento osseous dysplasia
fibrous dysplasia

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2
Q

common disease with unknown cause affects periapical bone; anterior mandible of patients older than 30; more common in black women

A

periapical cemento osseous

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3
Q

early lesions are well circumscribed and radiolucent ; with time, they become increasingly calcified; older lesions may be radiolucent with central opacifications

A

periapical cemento osseous dysplasia

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4
Q

periapical cemento osseous dysplasia mimics periapical disease, but the teeth are____

A

vital

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5
Q

older lesions contain numerous calcifications

A

periapical cemento osseous dysplasia

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6
Q
asymptomatic fibro-osseous lesion
women between 30 and 50 years
more commons in whites
posterior mandible
appears isolated, well delineated radiolucent to radiopaque lesion less than 1.5 cm
A

focal cemento osseous dysplasia

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7
Q

composed of numerous gritty pieces of soft fibrous ct and hard tissue

A

focal cemento osseous dysplasia

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8
Q

-a condition of disordered cementum and bone development; multiple quadrants in maxilla and mandible

A

florid cemento osseous

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9
Q

middle-aged black women who are older than 40; more than one quadrant; posterior regions; irregular opacification noted composed of dense, sclerotic bone, cementum, or both

A

florid cemento osseous dysplasia

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10
Q

diagnosed based on characteristic clinical presentation and radiographic appearance; can perforate mucosa; may lead to osteomyelitis, requiring surgery and antibiotics

A

florid cemento-osseous dysplasia

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11
Q

florid means

A

everywhere

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12
Q

focal means

A

one spot

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13
Q

a disease chraracterised by replacement of bone with abnormal fibrous connective tissue interspersed with varying amounts of calcifications; could be due to abnormal mesenchymal cell function; irregular trabeculae of bone; benign firbo osseous lesion

A

fibrous dysplasia

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14
Q

types of fibrous dysplasia

A

monostotic

polyostotic

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15
Q

involvement of a single bone; children and young adults; painless swelling or bulging of buccal plate

A

monostotic fibrous dysplasia

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16
Q

involvement of more than one bone; female children; long bones may exhibit bowing and an associated dull aching pain; skin lesions appearing as light-brown macules called cafe au lait spots

A

polyostotic fibrous dysplasia

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17
Q

which one has cafe au lait spots

A

polyostotic fibrous dysplasia

18
Q

several types of polyostotic fibrous dysplasia

A

craniofacial fibrous dysplasia
jaffe type
albright syndrome

19
Q

involves the maxilla with extension into the sinuses and adjacent zygoma, sphenoid, and occipital bones

A

craniofacial fibrous dysplasia

20
Q

involves multiple bones along with cafe au lait macules on skin

21
Q

characterized by endocrine abnormalities, precious puberty in females, stunting or deformity of skeletal growth in both sexes as a result of premature closing o the epiphyseal plates cafe au lait spots

A

albright syndrome

22
Q

painless enlargment of affected bone or bones; typically, a painless progressive, unilateral enlargement of the mandible or maxilla.
ground glass

A

polyostotic fibrous dysplasia

23
Q

ground glass

A

polyostotic fibrous dysplasia

24
Q

cellular fibrous ct interspered with irregularly shaped bony trabeculae; radiographic changes blend into the surrounding normal bone
surgical recontouring of bone for cosmetic reasons

A

polyostotic fibrous dysplasia

25
maloclussion, tipping and displacement of teeth ground glass maxilla common/painless/facial assymetry
fibrous dysplasia
26
chronic metabolic bone disease; resorption, osteoblastic repair, and remineralization of involved bone; unknown cause(could be virus); *men over age 50* maxilla commonly affected
paget disease of bone
27
paget disease is also called
osteitis deformans
28
enlargement is common; pain; spaces increase between teeth as bone enlarges ; may cause prosthesis to fit incorrectly
paget disease
29
radiograph: cotton wool; hypercementosis, loss of lamina dura
paget disease of bone
30
microscopically/histologically- reversal lines; mosaic bone pattern(numerous osteoblasts and clasts on surface in bony trabeculae pattern)
paget disease of bone
31
the serum alkaline phosphatase level is elevated in active disease; prominent reversal lines may create a pattern known as mosaic bone treatment is experimental-slowly progressive disease(no cure)
paget disease of bone
32
chronic progressive condition enlargement of the jaws, pain, neurologic complaints, increase spacing, loosening of teeth, cotton wool radiopaque pattern
pagets
33
well-vascularized ct containing multinucleated giant cells; occurs within bone; in children and young adults
central giant cell granuloma
34
anterior maxilla or mandible; young adults; may cause resorption or divergence of tooth roots; teeth are asymptomatic and VITAL; surgical excision
central giant cell
35
what is a lesion of bone that is radiographically identical to central giant cell
brown tumor
36
in patients with hyperparathyroidism is also very similar microscopically to what
central giant cell
37
a disease of bone that develops over a long period of time - result of calcium deficiency - young children(deficency in vit D) - adults(may be related to various health problems such as malabsorption syndrome)
osteomalacia
38
may be associated with delayed tooth eruption and periodontal disease
osteomalacia
39
an inherited form of vit D deficiency is called what
hypophosphatemic vit D-resistant rickets
40
osteomalacia--when this disease occurs in young children, it is usually caused by a nutritional deficiency of vit D,and associated with disease--?
rickets
41
have large pulp chambers with very long pulp horns; dentin has pronounced cracks, which leads to pulpal infections and fractures in enamel
hypophosphatemic vitamin D- resistant rickets