Leah Lampton Flashcards
(35 cards)
What developmental odontogenic cysts are derived from dental lamina
4
Most common (%)
Keratocysts (5%)
Calcifying odontogenic cysts
Lateral periodontal cyst
Gingival cyst of adult/newborn
What developmental odontogenic cysts are derived from reduced enamel epithelium
2
Most common (%)
Dentigerous cyst (20%) Eruption cyst
Where are inflammatory odontogenic cysts derived from
What are the inflammatory odontogenic cysts
3
Most common (%)
Epithelial cell rests of malassez
Periapical cyst
Radicular cyst (54%)
Paradental cyst
Dentigerous cyst
Origin and location
Development
Specific symptoms (3)
Types (3)
Commonest type of developmental cyst formed by fluid accumulation between crown and REE of impacted teeth
Usually 3rd molars or Max canines, males, 10-30
- Teeth fail to erupt so REE persists
- Fluid accumulates over crown and REE forms epithelial lining
Root resorption of adjacent teeth, displacement, discharge
- central variety
- lateral variety
- circumferential variety
Dentigerous cyst
Radiographically
Histology
Inflamed histology(3)
Complications (3)
Unilocular radiolucency associated with crown of unarupted tooth with well defined sclerotic border unless infected
Cystic lining - 2-4 layers cuboidal epithelium with flat interface to wall
Connective tissue wall- loosely arranged fibrous wall which may contain small islands of inactive odontogenic epithelial rests
Inflamed dentigerous cyst- increased collagenisation of wall, infiltration of chronic inflammatory cells, epithelial hyperplasia with rete ridges and squamous lining
Complications - ameloblastoma, squamous cell carcinoma, mucoepidermoid carcinoma
Eruption cyst
Origin and location Development Specific symptoms Histology Treatment
Soft tissue version of dentigerous cyst occurring due to separation of dental follicle from crown of erupting tooth within gingiva
Gingiva over erupting tooth
- Separation of dental follicle from crown of erupting tooth
Swelling with bluish tinge over unerupted tooth
Cystic lining- non keratinised stratified squamous epithelium
Connective tissue wall- fibrous wall with inflammatory cells
Cystic cavity- yellow protein fluid, may contain blood
Most burst spontaneously, alternatively incision and drainage allows for eruption
Keratocyst
Origin and location
Development
Associated genes or syndromes
Symptoms
Developmental cyst developing from undeveloped tooth, can be syndromic or sporadic and have a high reoccurrence rate
Tooth primordeum, males, 3rd decade, posterior mandible or maxilla
- Tooth primordeum degenerates and undergoes cystic changes
Gorlin Coltz syndrome, mutated PTCH gene
Missing tooth
Keratocyst
Radiographically
Histology
Multilocular radiolucent lesion
Cyst lining- 6-8 layers stratified squamous epithelium with flat interface, luminar surface has parakeratotic epithelium, basal layer shows basal palisading
Connective tissue wall- thick and friable, satellite cysts (reoccurrence)
Cystic cavity- transudate of serum, keratinous debris
Gingival cyst of adult
Origin and location
Development
Symptoms
Histology
Uncommon cyst developing in gingiva from remanence of dental lamina located in superficial part of alveolar mucosa
Buccaly on canine or premolar region of mandible
- Cystic degeneration of epithelial rests of serres in dental lamina
Small whitish bulge
Cystic epithelial lining with cavity filled with desquamated keratin
Periodontal cyst
Origin and location
Development
Radiographically
Histology
Uncommon non keratinised developmental cyst located lateral to root of vital tooth
Dental lamina remanence
- Proliferation of dental lamina remanence in jaw bone
Well defined Unilocular radiolucency lateral to involved teeth, with involved teeth vital
Glycogen rich clear cells
Radicular cyst
Origin and location
Development
Symptoms (5)
Types (3)
Commonest odontogenic cyst developed through inflammation
First molars, pulp necrosis following caries or trauma
- Inflammation of pulp and periradicular area causes apical periodontitis
- Abscess formation
- Periapical granuloma formation
- Inflammation of epithelial cell rests of malassez leads to cystic transformation
Caries, trauma, previous pulpitis, mobility, discharging sinus
- apical
- lateral
- residual
Radicular cyst
Radiography
Histology
Well defined radiolucency around apex
Loss of lamina along adjacent root
Root resorption
Radiographic appearance identical to granuloma
Cystic lining- uniform layer sse derived from ECRoM which may desquamate into lumen
Connective tissue wall- mixed inflammatory cell infiltrate
Cystic cavity- may contain dystrophic calcifications, cholesterol clefts, RBCs
Fibro osseous neoplasms:
Cemento ossifying fibroma
Location and aetiology
Histology
Radiography
Uncommon benign slow growing neoplasm causing painless swelling in mandible molar or premolar region
70-80% mandibular, age 20-40, females
Bone and cementum like areas surrounded by cellular fibrous tissue
Sharply defined encapsulated well circumscribed radiolucent lesion with varying amounts of radiopaque material, associated displacement or root fusion of adjacent teeth
Fibro osseous neoplasms:
Cemento ossifying fibroma
Variant - juvenile ossifying fibroma
Treatment
Juvenile ossifying fibroma is an agressive varient of COF found in under 15s
Regular lesions- enucleated
Large tumours- may require local resection and bone grafting if jaw distorted
Recurrence rare but densely mineralised lesions are relatively avascular and can develop into chronic osteomyelitis following dental extraction
Cemento osseous dysplasia
Aetiology
Management
Types (3)
A non neoplastic disturbance of growth and remodelling of bone and cementum, it is the most common fibro osseous lesion of jaw
90% in females, particularly african decent, 30-50
Do not require treatment except for cosmetic reasons
- periapical cemento osseous dysplasia (PA tissues)
- florid cemento osseous dysplasia (multiple teeth in more than one quadrant)
- focal cemento osseous dysplasia (single lesion on one tooth)
Periapical cemento osseous dysplasia
Location
Clinical features (2)
Histology (3)
Radiography (3 stages)
Cemento osseous dysplasia affecting the periapical tissues of one or more teeth with the histological features of cemento ossifying fibroma but without a sharply defined margin
Typically seen mandibular incisor region
Asymptomatic, affected teeth vital
Islands of bone within connective tissue stroma
Cellular fibrous tissue containing woven bone trabeculae and islands of dense cementum like bone
Progressive calcification leads to formation of solid bony mass
- Initially a localised radiolucency around roots of tooth resembling PA granuloma
- Intermediate stage with target like appearance due to mineralisation starting centrally
- Lesion grows to 8-10mm and becomes densely radiopaque with defined masses of cementum
Florid cemento osseous dysplasia
Clinical features (3)
Histology (4)
Radiography(2)
Cemento osseous dysplasia affecting multiple teeth in more than one quadrant
Frequently symmetrical, asymptomatic, affected teeth vital
Sheets or fused masses of relatively acellular cementum like tissue
Some patients develop associated solitary bone cysts
Cellular fibrous tissue containing woven bone trabeculae
Progressive calcification leads to formation of solid bony mass with resting and reversal lines
Target like appearance with central sclerosis
Lesion surrounded by outer zone of sclerosis
Focal cemento osseous dysplasia
Location
Histology (2)
Radiography (2)
Cemento osseous dysplasia forming a single lesion on one tooth
Typically post mandible
Cellular fibrous tissue containing woven bone trabeculae and islands of dense cementum like bone
Progressive calcification leads to formation of solid bony mass with resting and reversal lines
Well circumscribed with sharp defined margin
Varying amounts of radiopaque material
Non neoplastic genetic diseases:
Cherubism
Clinical features (3)
Histology (active vs quiescent lesion)
Radiography
Genetics (2)
Rare genetic condition affecting bones of usually lower jaw in which bone replaced by multilocular cyst like tissue growths making cheeks appear round and swollen
Firm painless bilateral swellings in jaws
Develops early childhood and regresses with skeletal maturation
Teeth frequently displaced or loosened
Loose fibrous tissue containing clusters of multinucleate giant cells
- active lesion: cellular lesion with many giant cells
- quiescent lesion: bone deposition within cellular stroma
Lesions appear radiographically as multilocular cysts
Autosomal dominant condition caused by mutated SH3BP2 gene
Twice as common in males
Fibrous dysplasia
Genetics
Radiography
Monostotic fibrous dysplasia
Polystotic fibrous dysplasia
Fibrous dysplasia is a growth distance of bone caused by somatic mutation in GNAS1 gene occurring in embryo and is associated with albrights syndrome It causes fibroblasts and osteoblasts to grow excessively
Radiographically margins merge with surrounding normal bone
Monostotic- causes enlargement of one bone M=F
Polystotic- widespread and may be associated with endocrine abnormalities
What is the most common benign tumours (2)
Ameloblastoma
Odontomes
What benign odontogenic tumours are of epithelial origin
3
Ameloblastoma
Squamous odontogenic tumour
Calcifying epithelial odontogenic tumour (pindborg tumour)
What are the benign odontogenic tumours of epithelial and ectomesenchyme origin
4
Odontomes
Ameloblastic fibroma
Adenomatoid odontogenic tumour
Calcifying odontogenic cyst
What is a benign odontogenic tumour of ectomesenchyme origin
1
Cementoblastoma