Tumors Flashcards

1
Q

Most common epithelial Odontogenic tumor

A

Ameloblastoma

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2
Q

Most common site for Ameloblastoma

A

Mandibular molar ramus area, can be associated with impacted teeth

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3
Q

Slow growing, painless and capable of causing large facial deformities

A

Ameloblastoma

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4
Q

Types of Ameloblastoma

A

Multicystic
Unicystic
Peripheral or extraosseous

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5
Q

Multilocular radiolucencies with well defined sclerotic margins - soap bubble or honey comb

A

Multicystic Ameloblastoma

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6
Q

Superficial saucerization of cortical plate, cup shaped radiolucency beneath elevated nodule

A

Peripheral or extraosseous ameloblastoma

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7
Q

Most common microscopic patterns of ameloblastoma

A

Follicular and plexiform

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8
Q

Tx if ameloblastoma

A

Simple Enucleation or en bloc / marginal resection

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9
Q

True mixed tumor epithelium and connnective tissue

A

Ameloblastic Fibroma

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10
Q

Mixed tumor similar to ameloblastic fibroma but contains odontoma

A

Ameloblastic Fibroma-odontoma

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11
Q

Molar ramus region, slow painless swelling, impacted molars, unilocular or multilocular radiolucent lesions with scalloped margins may contain calcified opaque structures

A

Pindborg tumor/ calcifying epithelial Odontogenic tumor

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12
Q

Sheets of large polygonal epithelial cells within connective tissue stroma with areas of amyloid that have concentric deposits, Liesegang rings

A

Pindborg tumor/ calcifying epithelial Odontogenic tumor

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13
Q

Females, 10-19 in anterior maxilla, asymptomatic tumor

A

Adenomatoid odontogenic tumor

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14
Q

Unilocular radiolucency surrounding unerupted canine crown, extends past CEJ

A

Adenomatoid Odontogenic tumor

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15
Q

Completely radiolucent but with fine snowflake calcifications, ductlike structures surrounded by thick fibrous capsule

A

Adenomatoid Odontogenic tumor

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16
Q

Agressive intraosseous lesion arising from odontogenic mesenchyme from dental pulp or follicular connective tissue

A

Odontogenic myxoma

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17
Q

Painless, slowly enlarging swelling, cortical expansion, teeth displacemeny and root resorption

A

Odontogenic myxoma

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18
Q

Unilocular or multilocular, margins irregular or scalloped, thin wispy trabeculae which gives soap bubble or tennis racket appearance

A

Odontogenic myxoma

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19
Q

Haphazardly arranged stellate, spindle shaped, round cells, loose myxoid stroma only few collagen fibrils

A

Odontogenic myxoma

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20
Q

Odontogenic tumor, proliferation of cementoblasts that form large mass o cementum and cementum like tissue

A

Cementoblastoma

21
Q

Proliferation of cementum, pain and swelling, teeth vital, mand 1st molar, radiopaque mass with thin radiolucent rim

A

Cementoblastoma

22
Q

Most common Odontogenic mixed tumor

23
Q

Hamartomatous lesion found over unerupted teeth containing enamel, dentin, pulp in either tooth shapes(compound) or solid, gnarled mass(complex)

24
Q

Asymptomatic non neoplastic bony growth covered by normal mucosa

A

Tori mandibularis

25
Tumor like lesion, replacement of medullary bone by cellular fibrous connective tissue causing the bone to become fragile
Fibrous Dysplasia
26
Expansion of bone, displaces maxillary sinus and obliterate it
Fibrous dysplasia
27
Types of fibrous dysplasia
Monosyotic Polyostotic
28
Alkaline phosphatase level increased in which type of fibrous dysplasia
Polyostotic fibrous dysplasia
29
Painless, unilateral swelling, ground glass, orange peel or finger print appearance
Fibrous dysplasia
30
Mandibular bucco lingual expansion, bulging of inferior border, ill defined lamina dura that blends with abnormal bone
Fibrous Dysplasia
31
Irregular shaped trabeculae of woven bone in fibrous connective tissue - Chinese characters
Fibrous dysplasia
32
Genetic disorder severe polyostotic fibrous dysplasia, unilateral cafe au lait spots, endocrine abnormalities
McCune Albright syndrome
33
Multiple, slow growing painless expansile bone lesions causes pathological fractures, premature puberty in females
McCune Albright syndrome
34
Connective tissue stroma with irregular woven immature bone. As ut matures more calcified structures
Ossifying fibroma
35
Benign fibro-osseous lesion of jaw arising from undifferentiated cells from PDL. Usually arise from tooth bearing areas
Ossifying fibroma
36
Reactive lesion to local factors, apex of vital teeth, mandibular anteriors periapical, asymptomatic, middle aged women, aftican. Osteolytic, cementoblastic, mature stage
Periapical cemento osseous dysplasia
37
Rare benign tumor of bone arising from osteoblasts, fast onset
Osteoblastoma
38
Well or ill defined round to oval radiolucency with areas of remineralization
Osteoblastoma
39
Colorectal polyps that become adenocarcinoma by fifth decade of life
Gardner’s syndrome
40
Multiple osteomas, Fibromas of skin, epidermal and trichilemmal cysts, abnormalities of the retina of eye
Gardener’s Syndrome
41
Multiple odontomas, multiple impacted and supernumerary teeth. Multiple jaw osteomas cotton wool appearance
Gardner’s syndrome
42
Benign, jaw, young females, anterior to molars, crosses midline, asymptomatic expansile
Central giant cell granuloma
43
Multilocular or Unilocular well demarcated but non corticated. Spindled fibroblasts and multinucleated giant cells in a stroma of collagen
Central giant cell granuloma
44
Tx of central giant cell granuloma
Curettage, steroid, calcitonin injections, interferon injections and bisphosphonates
45
Clonal proliferation of cells phenotypic characteristics of Langerhans cells
Langerhans cell disease
46
Floating in space. Most common form of landerhans cell disease
Eosinophilic granuloma/ chronic localized form Solitary or multiple bone lesions without visceral involvement
47
Chronic disseminating form of Langerhans cell disease with bone, skin and visceral organ involvement
Hand-Schuller-Christian syndrome
48
Lytic bone lesions, exophthalmos, Diabetes Insipidus
Chronic disseminating form of langerhans cell disease/ Hand-Schuller-Christian syndrome
49
Multiple radiolucent lesions, punched out, scooped out, floating in air, severe bone destruction, loose teeth, premature exfoliation, multinucleated giant cells, birbeck granules
Langerhans cell disease