Chapter 8 Nonneoplastic Diseases of Bone Flashcards
_____: refers to the abnormal and disordered production of cementum and bone
Dysplasia
______: They are well- circumscribed with distinct histology and radiographc features
Central cementifying Fibroma
(aka Ossifying fibroma)
Nonneoplastic diseases are not cancerous. Nonneoplastic diseases do not need to be removed.
A) The first statement is true. The second statement is false.
B) The first statement is false. The second statement is true.
C) Both statements are false.
D) Both statemetns are true.
A) The first statement is true. The second statement is false.
Nonneoplastic diseases are not cancerous but they still need to be removed to to exssessive growth that can interfere with surrounding tissues.
Another definition of ______ is, the abnormal production of cementum and bone.
Dysplasia
Which of the following is not a cemento-osseous displasia type?
A) Periapical cemento-osseos
B) Polyostatic cemento-osseos
C) Focal cemento-osseous
D) Florid cemento-osseous
B) Polyostatic cemento-osseos
______ dysplasia is defined as involvement of a single bone.
monostatic fibrous
______ dysplasia is defined as involvement of more than one bone.
Fibrous polyostotic
Name the three types of polyostotic fibrous dysplasia.
Craniofacial type
Jaffe type
Albright syndrome
What is the following describing:
- Relatively common disease of unknown cause that affects periapical bone
- Occurs most commonly in the anterior mandible of patients older than 30
- More common in women than men:
- Many studies indicate a predilection for black women
- Early lesions are well circumscribed and radiolucent; with time, they become increasingly calcified
- Teeth in the affected area are vital
Periapical Cemento-Osseous Dysplasia
What is the following describing:
- A condition of disordered cementum and bone development
- Usually occurs in black women older than 40 years of age
- Typically affects more than one quadrant in either the maxilla or mandible often in the POSTERIOR areas.
- Usually no bone expansion occurs
Florid Cemento-Osseous Dysplasia
What is the following describing:
- Masses of irregular opacification are noted that are composed of dense sclerotic bone, cementum, or both
- Best diagnosed on the basis of its characteristic patient history, clinical presentation, and radiographic appearance
- Asymptomatic florid cemento-osseous dysplasia does not require treatment
- If a patient is edentulous and the sclerotic bone perforates the mucosa- causing connection to bacteria in the oral cavity to the bone- complications may result in the need for antibiotic treatment and/or surgery
Florid Cemento-Osseous Dysplasia
What is the following describing:
- An asymptomatic fibro-osseous lesion
- Occurs in women between 30 and 50 years of age
- More common in white people than black people
- Occurs in posterior mandible
- Isolated, well-delineated radiolucent-to-radiopaque lesion
- Less than 1.5 cm in size
Focal Cemento-Osseous Dysplasia
What is the following describing:
- Developmental disease that is a genetic mutation
- Characterized by replacement of bone with abnormal fibrous connective tissue interspersed with varying amounts of calcification
- Histologically, it is a benign fibro-osseous lesion, with vascularized, cellular fibrous connective tissue interspersed with irregular trabeculae of bone
- Classic radiographic appearance of “ground glass”
Fibrous dysplasia
Name two types of fibrous dysplasia.
Monostatic fibrous dysplasia
Polyostatic dysplasia
What is the following describing:
- Is a developmental disease characterized by involvement of a single bone
- The posterior maxilla is more frequently involved than the mandible
- Most commonly diagnosed in children and young adults, with no sex predilection
- Clinical examination reveals a painless swelling or bulging of the buccal plate
- The disease usually extends into the maxillary sinus and surrounding bones called Craniofacial Fibrous Dysplasia AND THEN BECOMES POLYOSTOTIC
Monostatic fibrous dysplasia
What is the following describing:
- Characterized by involvement of more than one bone
- Typically occurs in children, with a female predilection
- The skull, clavicles and long bones are affected. When long bones are involved, they may exhibit bowing and an associated dull aching pain
- Patients may have skin lesions appearing as light-brown macules called café au lait spots
Polyostatic fibrous dysplasia
What is a type of polyostotic fibrous dysplasia that involves the maxilla with extension into the sinuses and adjacent zygoma, sphenoid, and occipital bones?
Craniofacial fibrous dysplasia
What is a type of polyostotic fibrous dysplasia that involves multiple bones along with cafe au lait macules on the skin?
Jaffe type
What is a type of polyostotic fibrous dysplasia that is characterized by
- endocrine abnormalities
- young children
- precocious puberty in females
- stunting or deformity of skeletal growth in both sexes as a result of premature closing of the epiphyseal plates.
- Diabetes and hyperthyroidism with café au lait spots
Albright syndrome
What is the following describing:
- Typically a painless, progressive, unilateral enlargement of the mandible or maxilla
- The classic radiographic appearance is a diffuse radiopacity looking like “ground glass”
Polyostotic Fibrous Dysplasia
What is the following describing:
- A chronic metabolic bone disease
- Characterized by resorption, osteoblastic repair, and remineralization of involved bone
- Unknown cause: May be due to a virus, genetic or environmental
- Most commonly occurs in men over age 50 years
- Involves the pelvis, femur, spinal column, tibia, and skull.
- The maxilla is more commonly affected than the mandible
- Enlargement of affected bone
- Patient often complains of pain
- Headache, dizziness from impingement on cranial nerves
- Spaces may increase between teeth as jaw bone enlarges
Paget disease
Radiographically, _______ will be a patchy radiolucency and radiopacity, “cotton wool” & have hypercementosis, loss of lamina dura, and obliteration of the periodontal ligament may occur
Paget disease
What is the following describing:
- May experience pain; not common
- Slow-growing lesion
- Destructive
- Unilocular or multilocular radiolucency
- Sclerotic or ill-defined borders
- Divergence of roots
Central Giant Cell Granuloma
What is the following describing:
- Pseudocyst – abnormal cavity that resembles a cyst but has no lining of epithelium
- Consists of blood-filled spaces surrounded by multinucleated giant cells and fibrous connective tissue
- Commonly seen in the long bones. Jaw lesions are rare.
- Radiographic: “Honeycomb” or “soap bubbles”
- Less than 30 years of age
Aneurysmal Bone Cyst
What is the following describing:
- Result of vitamin D deficiency causing a calcium deficiency and can be induced by certain tumors
- Rickets
- Hypophosphatemic vitamin D–resistant rickets
- Clinical characteristics
- Delayed tooth eruption
- Periodontal disease
- Pathologic fractures-
- due to poor bone mineralization
Osteomalacia
Central Giant Cell Granuloma
Paget disease
Paget disease
Paget disease ray “cotton wool” look
Paget Disease
(enlargement of bone)
Polyostotic fibrous dysplasia
Polyostotic fibrous dysplasia
Polyostotic fibrous dysplasia