Week 9 - Bone Formation and Resorption II Flashcards

1
Q

Architecture/shape of the tooth-associated facial and lingual cortical bone is dictated by

A

o Facial-lingual alignment of teeth
o Mesial-distal contour of CEJ
o Facial-lingual width of teeth
o Presence of enamel pearls or cervical enamel projections

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2
Q

Architecture/shape of the interproximal alveolar bone is dictated by

A

o Facial-lingual contour of the CEJ
o Mesial-distal tilt to the tooth
o Root proximity (roots that are close together result in thinner bone)
o Presence of enamel pearls
o State of tooth eruption (bone follows CEJ)

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3
Q

What is a fenestration defect?

A

An isolated “porthole”/window in the cortical bone that allows exposure of the underlying root surface
- Excessive buccal inclination (can happen in orthodontics/teeth moving too quickly or genetically)

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4
Q

What is a dehiscence defect?

A

A denuded area of cortical bone that extends through the marginal bone creating a “cleft-like” defect

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5
Q

What is an exostosis defect?

A
  • Area of bone formation that exceeds the average for a given anatomical area
  • The term is generally used in reference to the maxillary facial and lingual and mandibular facial
  • Typically not pre-cancerous
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6
Q

What are torus/tori?

A
  • An area of bone formation that exceeds average for a given anatomic area
  • The term is used in reference to the mandibular lingual or midline of the palate (torus palatini)
  • Don’t typically need to be removed unless they exhibit problems like rapid growth, pain, interfere with mastication, speech, or denture fabrication
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7
Q

What is a giant cell tumor?

A

Generally asymptomatic causing a painless expansion of bone. Usually a single lesion that can be wither unilocular or multilocular

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8
Q

What is giant cell tumor often confused with?

A

Often confused with ameloblastoma, periapical granuloma, or periapical cyst (consider biopsy to determine)

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9
Q

What is giant cell tumor histologically characterized by?

A

presence of numerous multinucleated giant cells in a stroma of ovoid and spindle shaped mesenchymal cells

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10
Q

What is multiple myeloma?

A

Malignancy of plasma cell origin that accounts for nearly 50% of all

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11
Q

What are multiple myeloma plasma cells like?

A

The abnormal plasma cells are typically monoclonal (arise from a single cell, all look exactly the same)

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12
Q

What do patients suffer from in multiple myeloma?

A

Patients frequently suffer kidney failure due to overload of circulating light chain protein (Bence Jones Protein) produced by the abnormal plasma cells and clot up the kidneys causing failure

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13
Q

What do patients histologically show in multiple myeloma?

A

shows monotonous sheets of neoplastic, variably differentiated, plasmacytoid cells that invade and replace normal host tissue

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14
Q

What do patients radiographically show in multiple myeloma?

A

Patients may exhibit “punched out” areas in the cranium. Such areas are filled with neoplastic plasmacytoid cells

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15
Q

What is osteogenic sarcoma?

A

A malignancy of mesenchymal cells that have the ability to produce osteoid or immature bone

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16
Q

What is one of the most common types of malignancies that start in bone?

A

Osteogenic sarcoma
**excluding hematopoietic neoplasms

17
Q

What are the most common symptoms of osteogenic sarcoma?

A

Pain and swelling are most common symptoms (**one of the few cancers in head and neck area that cause pain/swelling)

18
Q

What are radiographic findings of osteogenic sarcoma?

A

Radiographically patients findings vary from sense sclerosis to a mixed sclerotic-radiolucent lesion. About 25% of lesion exhibit a “sunburst” pattern

19
Q

How do enamel, dentin, cementum, and bone compare in overview?

A