scr - os & histopathology - tumours Flashcards

(44 cards)

1
Q

odontogenic tumours

A

majority asymptomatic often discovered due to:
- non eruption of teeth
- late stage bony expansion
- incidental finding
pain is usually due to pathological # or 2ndary infection

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2
Q

3 groups of odontogenic tumour

A
  1. epithelial -> ameloblastoma / adenomatoid odontogenic tumour / calcifying epithelial odontogenic tumour
  2. mesenchymal -> odontogenic myxoma
  3. mixed (both of above) -> odontoma
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3
Q

mixed tumours specifically

A

can have enamel / dentine formation due to concept of induction
1st formed dentine from odontoblasts which are mesenchymal in origin
ameloblasts mature & form enamel only when dentine starts getting laid down so present of dentine crucial for induction for maturation of ameloblast formation of enamel

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4
Q

odontogenic sources of epithelium

A

rests of malassez - from hertwig’s epithelial root sheath
rests of serres - from dental lamina
reduced enamel epithelium - from enamel organ

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5
Q

ameloblastoma

A

benign epithelial tumour
locally destructive but slow growing & typically painless
1% of OMFS tumours
4th-6th decades most common
80% posterior mandible
M>F

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6
Q

radiographic appearance of ameloblastoma

A

well defined bone surrounding pathology
well defined corticated margins
scalloped & multicystic
thick curved septa i.e. soap bubble appearance
primarily radiolucent

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7
Q

adjacent structures to ameloblastoma

A
  1. displacement; characteristic expansion pattern (expands in all directions fairly equally)
  2. thinning of bony cortices
  3. ‘knife edge’ external root resorption
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8
Q

histopathological criteria of ameloblastoma

A

can be:
follicular
plexiform
desmoplastic

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9
Q

plexiform form

A

shows fibrous tissue / stellate reticulum like tissue / ameloblast like cells
no CT capsule
so cells can grow & infiltrate into jaw bone & is one of the main reasons for high recurrence rate

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10
Q

follicular form

A

islands bordered by cells that resemble ameloblasts
tissue in middle of follicles is loose resembling stellate reticulum of tooth germ & can sometimes have cystic changes in follicle

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11
Q

management of ameloblastoma

A
  1. surgical resection with margin
  2. recurrence relatively common ~ 15%
  3. risk of malignant transformation <1% (ameloblastic carcinoma)
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12
Q

how would benign tumour appear in ultrasound (4)

A

well defined
encapsulated
peripheral vascularity
no lymphadenopathy

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13
Q

options for differential diagnosis for multilocular radiolucency in mandible

A

OKC
ameloblastoma
ameloblastic fibroma
odontogenic myxoma
odontogenic fibroma

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14
Q

follicular histopathology

A

tumour cells in follicular pattern
resemble enamel organ in developing tooth with a central mass resembling the stellate reticulum
surrounded by ameloblast like cells that display the typical reversed polarity, the nuclei are located away from the basement membrane opposite to what is usual

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15
Q

changes in the stellate area within the follicle

A

cystic breakdown - looks like large white spaces
squamous metaplasia
granular cell changes

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16
Q

plexiform histopathology

A

neoplastic epithelium arranged as a network of strands and irregular masses displaying the same cell layers as the follicular pattern with reversed polarity obvious
cyst degeneration in this type is mainly due to stromal degeneration

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17
Q

adenomatoid odontogenic tumour

A

benign epithelial tumour
3% of odontogenic tumours
most common 2nd decade
F>M
anterior maxilla

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18
Q

key about AOT

A

75% associated with u/e tooth, commonly maxillary canine

19
Q

radiographic criteria of AOT

A

unilocular radiolucency
majority have internal calcification / radiopacities which increase as tumour matures
margins well defined & corticated
may displace adjacent structures but external root resorption rare
very similar to dentigerous cyst

20
Q

difference between AOT & dentigerous cyst

A

AOT has
1. thicker cortical margins
2. attaches further down root (cyst attaches at CEJ)

21
Q

histopathological criteria of AOT

A

epithelial in origin
arranged in duct like structures (big hole) described as rosette appearance
distinctive with patchy calcification
well developed fibrous tissue capsule surrounding cells so removal of tumour straightforward surgically & recurrence rate is LOW

22
Q

calcifying epithelial odontogenic tumour

A

benign epithelial tumour
1% odontogenic tumours
most common 5th decade
M>F
posterior mandible most common
slow growing but can become large
1 in 2 associated with u/e tooth

23
Q

radiographic criteria of CEOT

A

variable presentation
uni or multi locular
well or poorly defined margins
internal septa - poor / fine / none

24
Q

odontogenic myxoma

A

mesenchymal benign tumour
3-6% of odontogenic tumours
most common in 3rd decade
F = M
Mandible > maxilla

25
radiographic criteria of odontogenic myxoma
well defined radiolucency +/- thin corticated margin small lesions = unilocular large lesions = multilocular soap bubble appearance of septa slow growth along bone before causing buccolingual expansion scallops between teeth but larger lesions may cause displacement; external root resorption rare
26
histopathological criteria of odontogenic myxoma
loose myxoid tissue with stellate cells may contain islands of inactive odontogenic epithelium no capsule = locally invasive
27
odontogenic myxoma management
curettage / resection depending on size high recurrence ~ 25% follow up important lower recurrence rate if unilocular
28
odontoma
benign mixed tumour technically a hamartoma malformation of dental tissue 1/5 - 2/3 of all odontogenic tumours most common 2nd decade F = M
29
odontoma similarities to teeth
mature to certain stage can be associated with other odontogenic lesions e.g. dentigerous cyst surrounded by dental follicle lie above IAN canal
30
2 types of odontoma
complex -> disorganised mass of dental tissue, more common posterior body of mandible compound -> ordered dental structures, may appear as multiple mini teeth, more common anterior maxilla
31
radiographic criteria of odontoma
well defined clump of radiopaque material
32
histopathological criteria of odontoma
both from mesenchymal & epithelial tissue enamel is inorganic so is dissolved during process of slide development; may not show on slide dependent on level of calcification
33
ossifying fibroma clinical criteria
slow growing wide age range mainly mandible similar to fibrous dysplasia but has capsule which is reflected in radiolucent line surrounding mass whereas dysplasia blends into the bone
34
histopathological criteria of ossifying fibroma
cellular fibrous tissue immature bone acellular calcifications
35
fibrous dysplasia
slow growing asymptomatic bony swelling due to bone being replaced by fibrous tissue active u20yrs of age can be single or multiple bone maxilla > mandible can be syndromic - albright's syndrome (melanin pigment & early puberty)
36
radiographic criteria of fibrous dysplasia
margins often blend into adjacent bone bone maintains approximate shape initially becomes more radiopaque as lesion matures can have variable appearances i.e. cotton wool / amorphous
37
histopathological criteria of fibrous dysplasia
fibro osseous fibrous replacement of bone no capsule separating it from normal bone bone remodels and increases in density
38
rarefying osteitis
localised bone loss in response to inflammation always occurring 2ndary to another form of pathology if at apex of tooth consider apical periodontitis / PA granuloma / PA abscess
39
sclerosing osteitis
localised increase in bone density in response to low grade inflammation most common around apex of tooth with necrotic pulp PA radiopacity often poorly defined may eventually lead to external root resorption if chronic
40
osteosarcoma
malignancy of bone normally in 30s if older generally due to paget's mandible > maxilla recurrence, local destruction & metastases
41
paget's disease
usually >40ys M > F aetiology unknown serum biochemistry shows raised alkaline phosphatase disease of disturbed bone turnover -> deposition & resorption occur at the same time so bone becomes soft & deformed then calcifies in deformed shape
42
dental changes with paget's
loss of lamina dura hypercementosis migration (due to bone enlargement)
43
histology of paget's
reversal lines - indicate change in turnover which can be very darkly stained will burn out itself osteoclastic & osteoblastic activity
44
tx of paget's pt
xla of teeth can be difficult due to hypercementosis / pathological # of mandible / affected bone tends to develop osteosarcoma dense bone harder to LA MRONJ risk as on anti resorptives osteosclerotic stage = less vascular so little bleeding so increased risk of dry socket / MRONJ osteolytic stage = more vascular so lots of bleeding