Omfr Master Document
Omfr Master Document
Omfr Master Document
M Notes
SYNDROMES/SYSTEMIC......................................................................................................................................................................... 2
CHERUBISM...................................................................................................................................................................................................... 2
NEVOID BASAL CELL CARCINOMA SYNDROME (NBCCS)...........................................................................................................................................3
FIBRO-OSSEOUS LESIONS....................................................................................................................................................................... 4
FIBROUS DYSPLASIA............................................................................................................................................................................................ 4
OSSIFYING FIBROMA........................................................................................................................................................................................... 5
OSSEOUS DYSPLASIA...........................................................................................................................................................................................6
ODONTOMA..................................................................................................................................................................................................... 8
OTHER RADIOPAQUE LESIONS OF THE JAWS........................................................................................................................................... 9
ANTRAL PSEUDOCYST......................................................................................................................................................................................... 9
CEMENTOBLASTOMA........................................................................................................................................................................................ 10
SCLEROSING OSTEITIS/CONDENSING OSTEITIS.......................................................................................................................................................11
DENSE BONE ISLAND (DBI)............................................................................................................................................................................... 11
RADIOLUCENT LESIONS OF THE JAWS................................................................................................................................................... 12
LATERAL PERIODONTAL CYST..............................................................................................................................................................................12
DENTIGEROUS CYST.......................................................................................................................................................................................... 13
KERATOCYSTIC ODONTOGENIC TUMOR (KCOT).....................................................................................................................................................14
AMELOBLASTOMA............................................................................................................................................................................................ 15
ODONTOGENIC MYXOMA.................................................................................................................................................................................. 16
NASOPALATINE DUCT CYST................................................................................................................................................................................ 17
PSEUDOCYSTS...................................................................................................................................................................................... 18
SIMPLE BONE CYST (TRAUMATIC BONE CYST).......................................................................................................................................................18
LINGUAL BONE DEFECT (STAFNE DEFECT).............................................................................................................................................................19
PERIAPICAL RADIOLUCENCY OF INFLAMMATORY ORIGIN (PRIO)...............................................................................................................................19
VARIOUS RADIOGRAPHS...................................................................................................................................................................... 20
DIFFERENTIAL DIAGNOSIS FLOWCHARTS.............................................................................................................................................. 26
A VERY LARGE TABLE............................................................................................................................................................................ 47
Syndromes/Systemic
Cherubism
= Rare Autosomal Dominant condition
Radiographic
Features
Page | 2
Clinical Features Variable phenotypes including:
- Multiple Basal Cell Carcinoma of the skin, Palmar and planting pitting, Skeletal abnormalities (bifid ribs,
vertebral fusion, polydactyly, temporoparietal bossing), Calcified Falx Cerebri.
- Multiple KCOTs
- BCC most frequent in North Europeans
- Multiple KCOT most frequent in East Asians
- Presents in 20-30s (10 years earlier than single KCOTs)
Page | 3
Fibro-Osseous Lesions
(Fibrous Dysplasia, Ossifying Fibroma, Osseous Dysplasia, Odontoma)
Fibrous Dysplasia
- Symptomatic regional alteration of bone in which the normal architecture is replaced by fibrous tissue and
nonfunctional trabeculae-like osseous structures; lesions may be monostotic or polyostotic, with or without
associated endocrine disturbances.
Clinical Features
Site More often in the Mandible, apical to premolars and molars (superior to IAN
canal)
When in Maxilla -> Canine fossa area
Shape Well Defined, encapsulated with a thin RL line
- cortex may appear thickened and sclerotic
Size
Shade Mixed RL/RO -> Similar to Fibrous Dysplasia (ground glass, cotton-wool)
Surroundings Beach Ball expansion
Thinning (but still intact) of the cortical borders of the jaw
May resorb Teeth
- Lamina Dura is missing
Density
Displacement May displace IAN and expand cortical plates
Displacement of Maxillary sinus floor
Displaces adjacent teeth
Diameter
Differential Dx Fibrous Dysplasia
Osseous Dysplasia
Complex Odontoma
Tx Surgical Enucleation + Curettage
Local Excision + Block Resection
Osseous Dysplasia
- Diffuse asymptomatic radiopaque and radiolucent intraosseous areas of osseous tissue that involve one or both arches.
Focal variant: a single lesion, affecting only 1 sextant/tooth
Radiographic
Features
Antral Pseudocyst
- retention of fluid in the lining of the sinus
Radiographic
Features
Radiographic
Features
Adjacent teeth
- Rare to see root resorption
- Very rare to see displacement
- PDL space is visible and separates the root from the lesion
Density
Displacement Displacement is very rare
Diameter
Differential Dx Sclerosing Osteitis -> SO has an associated widened PDL and is centered around the root apex
Osseous Dysplacia, Cementoblastoma -> Both of these have RL rim
Tx No Tx
Radiolucent Lesions of the Jaws
(Lateral Periodontal Cyst, Lateral Radicular Cyst, Dentigerous Cyst, Nasopalatine Duct Cyst, Simple Bone Cyst) (Ameloblastoma,
Keratocystic Odontogenic Tumor, Odontogenic Myxoma)
- Well defined radiolucencies: consider cysts
o cysts rarely cause root resorption compared to neoplasms and inflammation
- Poorly defined radiolucencies: consider inflammation and malignancy
Clinical Features
- Often Asymptomatic
- Tooth is vital
Radiographic
Features
Clinical Features
Central: Attached to CEJ on both sides with the entire body of the cyst above the CEJ
Lateral: Only attached to 1 side of the CEJ, cyst is coronal to the CEJ on the other side
Circumferential: Similar to central, but portions of the cyst are apical to the CEJ
Radiographic
Features
Ameloblastoma
- A benign and locally aggressive neoplasm of odontogenic epithelium that has a wide spectrum of histologic patterns resembling early
odontogenesis (enamel organ)
Odontogenic Myxoma
- An aggressive intraosseous lesion derived from embryonic connective tissue associated with odontogenesis and primarily consisting of a
mucoid ground substance with widely scattered undifferentiated spindled mesenchymal cells, similar to embryonic dental papilla
Clinical Features - Rare
- Painless, slowly growing swelling of the jaw
Radiographic
Features
Adjacent teeth:
- Causes tooth displacement (less than ameloblastoma)
- Rarely causes resorption
Density
Displacement
Diameter
Differential Dx Ameloblastoma
KCOT
Central Giant Cell Granuloma
Tx Resection
Nasopalatine Duct Cyst
- An intraosseous developmental cyst of the midline of the anterior palate, derived from the islands of epithelium remaining
after closure of the embryonic nasopalatine duct.
Clinical Features
Radiographic
Features
Site Centered in the maxillary midline within the nasopalatine foramen or canal
Shape Well defined corticated border, round or ovoid in shape
- Anterior nasal spine may be superimposed giving it a heart shape
Size
Shade RL
Surroundings May expand the labial or palatal cortices of the maxilla
Adjacent teeth
- May displace roots so they diverge
- Root resorption is possible
Density
Displacement May displace the floor of the nasal fossa superiorly
Diameter
Differential Dx PRIO -> Check to ensure the PDL is intact and separate from this lesion
Tx Enucleate
Pseudocysts
Simple Bone Cyst (Traumatic Bone Cyst)
- Asymptomatic intraosseous empty cavity of young patients located primarily within the mandible, lined by a thin loose
connective tissue membrane and is adequately treated when blood enters the space during an intraosseous biopsy.
Clinical Features
- Commonly in children and teeths
- Usually asymptomatic
- Primarily in the Mandible
- Associated teeth are vital
Radiographic
Features
Site Almost all are in the mandible -> most common in the posterior
Shape Well defined, delicately (sometimes not visible) corticated border
- Scallops between roots and teeth
Size
Shade RL
Surroundings May expand the bone if large, otherwise they prefer to scallop along the inside
of the bone
Adjacent teeth
- Usually no effect, Lamina dura is usually intact
Density
Displacement
Diameter
Differential Dx Aneurysmal Bone Cyst
Lateral Periodontal Cyst
Odontogenic Myxoma
Unicystic Ameloblastoma
Radicular Cyst
KCOT
Central Giant Cell Granuloma
Tx Monitor
Lingual Bone Defect (Stafne Defect)
A developmental concavity of the lingual cortex of the mandible, usually in the third molar area, caused by overextension of an accessory
lateral lobe of the submandibular gland, and has the radiographic appearance of a well-circumscribed cystic lesion within the bone, usually
below the inferior alveolar canal.
Clinical Features - Anatomic indentation of the posterior lingual mandible
- Always under the IAN Canal
- Asymptomatic
- Found later in life (5th decade) -> So not associated with mandibular fracture really
Radiographic
Features
Radiographic
Features
Cherubism
Dentigerous Cyst
A: Unicystic Ameloblastoma
B: Solid Ameloblastoma
C: Desmoplastic Ameloblastoma
KCOT
KCOT
Odontogenic Myxoma
Giant Cell Radiopaque Ground glass, Md:Mx = 2:1 66% Poorly Resorption teeth, Displace teeth, a. FOL/COF (ground glass)
Granuloma/Tumor multilocular, if defined lamina dura IAN inferiorly,
1st 2 Decades ant to b. Ameloblastoma/odontogenic
(or Central Giant granular wispy malignancy missing Expands cortical
1st molar Md or myxoma (b/c multilocular)
Cell Lesion septa* often Mx, plate Mx & Md
cuspid in Mx,
Md well (undulating),can
Older more
defined destroy Mx plate
posterior
= malignant
appearance
COD – Focal 3 phases; Round, oval Ant. Md apex tooth; Well defined No resorption No a. (mature) benign
PCD Young solitary, Lamina Dura lost cementoblastoma
Early – Rlucent, Seldom >1cm,
Midle age
Mixed – mixed, Can displace jaw b. periapical abscess/cyst
unilateral,
Mature – Rpaque and antrum
c. periapical granuloma
center & Rlucent Old bilateral
boarder often
continuous with
PDL*
COD - Florid PCD in 3-4 quads or a. Paget’s (cotton wool,
extensive in one jaw hypercementosis)
b. chronic diffuse sclerosing
osteomyelitis (cementum like
masses)
d. fibrous dysplasia
e. cementifying/ossifying fibroma
Odontoma Radiopaque = or > Compound (bag Complex – Md 1st & Complex Well defined, Prevent eruption a. COF (odontoma more
adjacent tooth of teeth)* 2nd molar area, smooth or of teeth, Lg radiopaque)
– large
Compund – ant Mx irregular, Complex expand
Compou b. PCD (pcd more centered)
cortical jaw
– crown of nd – size
boarder c. cementoblastoma
unerupted canine of tooth
Cementoblastoma Radiopaque Wheel spoke Md 1st Premolar – Well defined, External root Expansion of a. Solitary PCD
pattern*, Molar, Rlucent Halo resorption, cortical plates,
b. COD (Rlucent band)
Round, B-L just inside Obscures PDL Displace teeth
Fused w/ roots, c. DBI
expansion cortical
boarded
Lesion Shade Shape Site size surroundings Diameter density displacement DDX
Garnder’s Uniformly Rpaque bony trabeculae Angle of Md (look well-defined
Syndrome (multiple for multiple
osteomas) impacted
supernumerary
teeth)
Periapical RadioLucent Unilocular, Tooth apex (assoc. Abcess = Ill Widening of Abcess: Often > a. PCD (early)
Inflamatory Lesion spherical, w/ carious/resto’d defined PDL, can have 1.5cm expansive
b. DBI (for sclerosing ostitis)
PA Abcess (acute) teeth) Granuloma/Cy more bone and displacing*,
Granuloma st have capsul formation = PA Granuloma:
(chronic) sclerosing ostitis, Often < 1.5cm
Cyst(after bone resorption = non-displacing,
granuloma) PA rarefying in chronic -
ostitis external root
resorption, may
destroy cortical
boundaries
Residual Cyst PA Cyst minus the
tooth
Lateral Periodontal RLucent Round/oval Md 2nd premolar – < 1cm Well defined, Resorbs Lamina a. Small KOT (b/c location & x-
Cyst lateral incisor, prominent dura, Lg cysts ray appearance)
Later root surface cortical can cause b. Mental foramen (location)
boundary expansion
c. Radicular Cyst
Dentigerous Cyst RLucent unilocular 3rm molars and Mx Well No root Displaces a. hyperplastic follicle
Canines, w/n 1mm Circumscribed, resorption but can affected tooth
b. OKC ( not at CEJ, doesn’t
of CEJ* & around resorb adjacent apically,
resorb/expand as much)
crown of unerupted teeth expands corical
or supernumery bone, displaces c. ameloblastoma – unicystic
teeth (mesiodens teeth & IAN, (early stage)
Mx) grows into
d. Radicular cyst at apex of
antrum,
primary tooth (looks like DC of
crown of 2ndary)
Simple Bone Cyst Rlucent Unilocular Post. Md Variable Lost lamina dura, Generally no a. KOT (b/c longitudinal growth
(traumatic BC) (scalloped), can boarder no tooth expansion of w/ little expansion & scalloped
have septae resorption cortex boarder)
(longitudinal
b. Dentigerous cyst (if
growth)
associated with impacted tooth)
Odontogenic Round/oval or 80% Md, 60% 3rd Well Defined Can resorb roots Little B/L a. Dentigerous cyst (b/c
Keratocyst (OKC) scalloped, expansion, pericoronal center)
molar, Epicenter
(KOT) uni/multilocular Displace IAN
sup. To IAN b. Ameloblastoma (b/c
inf., grow into
multilocular and scalloped)
antrum
c. Odontogenic myxoma (b/c
multilocular & mild expansion)
d. Simple bone cyst (b/c scalloped
& minimal expansion)
Lesion Shade Shape Site size surroundings Diameter density displacement DDX
Gorlin-Goltz multiple a. Cherubism
Syndrome (multiple odontogenetic
b. Multiple dentigous cysts
KOT) keratocysts in Md
molar/premolar &
Mx 3rd molar
Ameloblastoma RLucent unilocular Post Md, can be Larger Well defined, Extensive Root tooth a. Dentigerous cyst – (b/c small
(Unicystic) (early) or occlusal to tooth posterior corticated and Resorption** displacement, unilocular if surround crown of
(also mentioned are multilocular bud , smaller sclerotic thinning of unerupted)
polycystic & (advanced): anterior margins cortical plate &
b. OKT (b/c internal boney septae
peripheral) Soapbubble or B/L expansion
honeycomb – multilocular)
c. odontogenic myxomas (b/c of
septa)
d. Giant Cell Granuloma (b/c
Septae)
e. Ossifying Fibroma (b/c septae)
Odontogenic RLucent 50% mutilocular Md premolar/molar Poorer defined Rare root Tendency for a. Simple bone cyst (b/c scallops
Myxoma resorption longitudinal b/w roots of teeth)
– Tennis
growth (may get
Racquet**, b. Septae list
B/L exp with Lg
fusiform
lesion),
expansion
Displaces teeth
Dense Bone Island RPaque Md premolar/molar, Well defined, May cause root a. Periapical Cemento Dysplasia
(5 or more think DBI vs SO: no capsule or resorption (on (Rpaque)
Gardner’s margin vital tooth & self-
DBI if not assoc. w/ b. Periapical sclerosing osteitis (if
syndrome) limiting) if
tooth, at apex)
involving tooth
Or a non-carious,
unrestored tooth;
SO if carious,
heavily resto’d tooth
Sclerosing Osteitis RPaque Premolar/molar, No bone a. DBI
(response to PA around tooth apex expansion
b. Cementoblastoma (b/c Rpacity
inflammation)
near root)
Stafne bone defect RLucency Round, ovoid, Submandibular Well Defined, Readily Differentiated
lobulated gland fossa, close to dense sclerotic
a. If rare and above IAN – other
inf boarder of Md, boarder,
odontogenic lesion
below IAN* Thicker on
superior
aspect*
Nasopalatine duct RLucent Round or oval, Nasopalatine Well defined, Occasional root Expand bone, a. Lg incisive foramen
cyst may be heart foramen or canal corticated resorption displace teeth
shaped b/c of (b/w apex of 11- (centrals roots b. Radicular cyst (only if cyst
superimposition 21)* diverge), can associated with central incisor
of anterior nasal displace floor of apex b/c it’s asymmetric)
spine nasal fossa
Stylohyoid complex RPaque (seen on Long tapering Mastoid process
PAN) thin process toward hyoid bone,
(thicker at base)