A. Odontome

B. Impacted supernumerary tooth

D. Impacted 3rd molar

A. Globulomaxillary cyst

C. Periapical cyst

D. Nasopalatine cyst

B. Paradental cyst

C. Eruption cyst

D. Radicular cyst

B. Dentigerous cyst

C. Keratocyst

D. Clacifying epithelial odontogenic cyst

A. Squamous cell carcinoma

C. Osteogenic sarcoma

D. Osteoclastoma

A. Adenomatoid odontogenic tumor

B. Pleomorphic

C. Warthins tumor

B. 3-4 mm

C. 1-2 mm

D. 2-3 mm

A. Has low recurrence rate

B. Can be treated by aspiration

C. Occurs due to infection periapically

A. Compound odontoma

B. Calcifying odontogenic cyst

C. Amebloblastic fibroodontoma

A. 1-2 cell thick

C. 15-20 cell thick

D. 2-4 cell thick

A. Primordial cyst

C. Dentigerous cyst

D. Mucocele

B. B and C

C. Has low protein content

D. High recurrence rate

A. None of the above

B. Ameloblastoma

C. Odontogenic keratocyst

B. All of these

C. Osteomas

D. Pagets disease

A. None of the above

C. Increased pressure within the cyst

D. Immune mediated bone destruction

B. All of the above

C. Adeno carcinoma

D. Fibrosarcoma

B. Marsupialization

C. Surgical Excision

D. Excise the lesion

A. Basal layer of cells

B. Stratum intermedium

C. Stratum corneum

D. Dental lamina

A. Enucleation

B. Excision

D. Irradiation

A. Static bone cavity

B. Aneurysmal bone cyst

C. Ameloblastoma

A. Grinspan syndrome

B. Goldenhars syndrome

C. Gardners syndrome

A. Enameloma

B. CEOT

C. Odontoma

B. It is more common in mandible

C. Expansion of bone clinically seen

D. May be filled with thin straw coloured fluid

A. Peripheral palisading with central stromal retraction artefact

C. Peripheral palisading cellular strand with peripheral loose stellate reticulum

D. Central loose stellate reticulum shows marked nuclear atypia and numerous mitotic

B. Non-Functional

C. Anatomically benign

D. clinically persistent

B. Sun-burst appearance

C. Cherry -blossom appearance

D. Onion peel appearance

A. Dental cyst

B. Dentigerous cyst

C. Simple bone cyst

A. Tennis racket

B. Irregular

C. Linear

A. A & C

C. Odontogenic ghost cell tumor

D. Keratcysticodontogenic tumour

A. Diskeratinised

B. Non-Keratinised

C. Orthokeratinised

A. thyroid disorders

B. Cherubism

C. Odontogenic keratocyst

B. Periapical abscess

C. condensing osteitis

D. None of the above

A. Friability of the epithelial lining

C. Continued proliferation of rests of dental lamina

D. Increased mitotic activity of the epithelial lining

B. Also known as Amebloblastoma

C. is a complication of dentigerous cyst

D. A tumour from embrynomal cells of developing teeth

A. Nasolabial

B. Median palatal

C. Globulomaxillary

A. Teacher collin syndrome

B. Downs syndrome

D. Gorlin Goltz syndrome

A. Haphazardly arranged calcified mass

B. All of the above

C. Mixed tissue of dental origin with no resemblance to tooth structure

B. Ramus of mandible

C. Anterior mandible

D. Posterior maxilla

A. Stellate shaped cells

B. Stratified squamous epithelial cells

D. Polyhedral epithelial cells

A. In mandibular body

B. In periapical region

D. In teeth in which crown development is completed

A. Resection of jaw

B. Pulpectomy

D. None of the above

A. Epidermoid carcinoma

B. Warthins stumour

C. Pleomorphic adenoma

A. Enucleation

B. Enbloc resection

D. Enucleation with cauterization

A. Nasoalveolar cyst

C. Globulamaxilary cyst

D. Periapical cyst

A. Excision biopsy

B. CT Scan

C. Pet Bone scan

B. Fibroma

C. None of the above

D. Papilloma

A. Mixed cellular inflammatory infiltrate

B. Antiepithelial antibodies

D. Scattered infiltrate with ill-defined lower border

B. Early enamel caries

C. Advanced enamel caries

D. Cemental caries

A. Lichen planus

C. Verrucous vulgaris

D. Bullous pemphigoid

B. Ptosis

C. Flushing

D. Anhydrosis