Keywords
jaws - tumor and tumor-like lesions - increased bone density - cone beam computed
tomography - imaging
Lesions with Preferential Periapical Location
Lesions with Preferential Periapical Location
Cementoblastoma
Cementoblastoma is a rare neoplasm of cementoblasts around the apex of a tooth root.[1] The mandible is more frequently involved than the maxilla with predilection of the
premolar or first molar of the mandible.[2]
[3] Children and adults < 30 years are usually affected.[1]
[2]
On panoramic radiographs and cone beam computed tomography (CBCT), the lesion appears
as a well-delineated round radiopaque mass of disorganized cementum often surrounded
by a thin radiolucent halo of nonmineralized germinative cells.[2] Cementoblastoma typically fuse with the root of one or more teeth and may invade
the root canal and pulp chamber.[4] Because of the intimate relationship with the root of the teeth, tooth extraction
may be difficult.[3]
Cemento-ossifying Fibroma
Cemento-ossifying fibroma is a benign neoplasm composed of fibrous tissue and mineralized
material, often found in the third and fourth decades with a marked female predilection.[5]
[6] Clinical presentation consists of a painless slow-growing mass that may cause facial
asymmetry.
On panoramic radiographs and CBCT ([Fig. 1] and [Fig. S1]), the lesion is usually mixed radiopaque-radiolucent and less commonly either radiolucent
or radiopaque. Advanced lesions become more radiopaque due to progressive matrix mineralization.
The lesion is well delineated and grows concentrically with buccolingual expansion.
Large lesions may cause tooth displacement and root resorption.[7] The mandibular canal may be displaced inferiorly, whereas in fibrous dysplasia the
canal may be displaced in any direction.[8]
[9]
Fig. 1 Cemento-ossifying fibroma of the maxilla. (a) Axial and (b) sagittal reformatted CBCT images show a well-delineated radiopaque lesion with ground-glass
appearance in the left anterior maxilla. Note some intralesional radiolucent foci
(white arrows) and resorption of the root of tooth 22.
Periapical Cemento-osseous Dysplasia
Although its precise etiology has not been unraveled, periapical cemento-osseous dysplasia
(PCOD) is believed to be a reactive process resulting from proliferation of connective
tissue within the periodontal membrane.[2]
[3] PCOD typically presents as an asymptomatic lesion in the bone around the root apices
of the mandibular incisors of middle-aged black women. Some lesions can be painful.[3]
Radiographically, three stages may be seen depending on the age of the lesions: initially,
the lesion is well defined and radiolucent (osteolytic stage), followed by a mixed radiolucent-radiopaque stage ([Fig. 2]), with a dense central core (cementoblastic stage), and finally a mineralized radiopaque mass surrounded by a thin radiolucent zone
may develop (mature inactive stage). The tooth remains vital in contradistinction to the devitalized tooth seen with
periapical granuloma.[10]
Fig. 2 Periapical cemento-osseous dysplasia, cementoblastic type. (a) Panoramic and (b) sagittal reformatted CBCT images show a mixed radiolucent-radiopaque lesion around
the apex of the left mandibular canine at the left anterior mandible with a dense
central core (arrow).
The term florid cemento-osseous dysplasia (FCOD) is used for a massive involvement of periapical cemental dysplasia involving
two of four quadrants of the tooth-bearing areas of the jawbones.[2]
[11]
[12] It is most frequently seen in the mandible of middle-aged black women, although
it may also occur in whites and Asians.[1]
[3] The lesion is found incidentally during routine dental examination and is often
asymptomatic or may present with pain.[11]
On radiographs and CBCT, FCOD presents as multifocal mixed osseous changes in the
jawbones.[2] There is often bone expansion. Sclerotic lesions do not fuse with the tooth root
and are located above the mandibular canal.[13]
FCOD usually has no hereditary basis, but familial cases have been reported. Familial
FCOD has no demographic predilection, presents at a younger age, and may progress
more rapidly than its sporadic counterpart.[11]
The differential diagnosis on imaging includes fibrous dysplasia, Paget's disease,
Gardner's syndrome, chronic sclerosing osteomyelitis, and osteoblastic bone metastasis.[11]
[12]
Fibrous dysplasia (FD) is often polyostotic and involves the maxilla more frequently
than the mandible.[11] It is typically unilateral and often extends into contiguous bones such as the zygoma
and sphenoid.[11] FD may be radiolucent in the initial stage but typically has a ground-glass appearance
and may cause superior displacement of the mandibular canal.[3]
[14]
Paget's disease is also often polyostotic but rather involves the entire mandible
and is characterized by elevated alkaline phosphate levels, whereas laboratory findings
in FCOD are normal.[12]
Gardner's syndrome is not restricted to the tooth-bearing area and may involve other
bones than the jawbones.[11]
In chronic osteomyelitis, usually one bone segment is involved and the lesion is poorly
circumscribed, whereas FCOD is seen as multiple round or lobulated opaque masses.
Chronic osteomyelitis usually involves the body of the mandible from the alveolus
to the inferior border and may extend into the ramus.[12] However, due to a decreased vascularity of the lesion, FCOD may predispose to chronic
infection and pathologic fracture with poor healing.[11]
Asymptomatic FCOD needs no surgical treatment. A wait-and see policy is recommended
with imaging follow-up every 2 to 3 years.[11]
Condensing Osteitis
Condensing osteitis, also known as focal sclerosing osteomyelitis, represents a mild
focal form of sclerosing osteomyelitis arising in the posterior mandible at the apices
of the premolar or molar teeth.[15] It is the most common sclerotic lesion of the jaw and usually affects children and
young adults.[13]
Radiologically or on CBCT ([Fig. 3]), it appears as a focal area of well-circumscribed or ill-defined bone sclerosis
surrounding the dental roots, often with inflamed or necrotic dental pulp.[11] The lesion may be single or multiple.[4]
Fig. 3 Condensing osteitis. (a) Panoramic reformatted CBCT image demonstrates a radiopaque lesion adjacent to the
apex of tooth 46. The lesion has spicular borders (arrow). (b) Axial reformatted CBCT image shows blending of the spicular borders with the adjacent
trabeculae (arrowheads).
Idiopathic Osteosclerosis
This incidental lesion presents radiographically as a radiopaque area adjacent to
the tooth apex or interradicular region, most commonly in the premolar or molar region.
It occurs in young asymptomatic patients and may be multifocal.
Radiographically or on CBCT ([Fig. 4]), the lesion has sharp angular margins.[13] This lesion resembles a dense bone island, but in the latter, there is no specific
relationship with the dentition. A typical dense bone island has spiculated margins.
Fig. 4 Idiopathic osteosclerosis. (a) Panoramic reformatted CBCT image showing a well-defined radiopaque lesion in the
left mandible between the roots of tooth 36 and 37 (arrow). There is root displacement
of 36 and 37. (b) Axial reformatted CBCT image confirms the radiopaque lesion in the left mandible
(arrow). There is an intimate relationship with the mandibular canal (arrowhead).
(c) Sagittal reformatted CBCT image confirms the intimate relationship with the mandibular
canal (arrowhead) and the dental roots (arrow). The lesion blends into the buccal
and lingual cortex. Note some spiculation at the inferior aspect of the lesion (thin
arrow).
Lesions with Preferential Pericoronal Location
Lesions with Preferential Pericoronal Location
Odontoma
Odontomas are hamartomas originating from differentiated epithelial and mesenchymal
cells (ameloblasts and odontoblasts) and composed of enamel and dentin.[16]
[17] Odontomas are the most common odontogenic neoplasms. They are most prevalent in
children and young adults.[2]
[15]
There are two macroscopic types. The compound odontoma consists of multiple denticles
or small teeth-like structures. The complex odontoma does not resemble a normal tooth
and appears as an amorphous calcified mass.[17]
Radiographically, the compound type ([Fig. 5] and [Fig. S2]) consists of multiple small radiopaque teeth-like structures surrounded by a thin
radiolucent halo. The complex odontoma ([Fig. 6]) presents as an irregularly shaped and amorphous radiopaque mass, also surrounded
by a thin radiolucent halo.[18]
Fig. 5 Compound odontoma. (a) Axial and (b) coronal reformatted dental CT images show multiple small radiopaque tooth-like structures
at the left anterior hemimandible with surrounding radiolucent halo (arrows).
Fig. 6 Complex odontoma in an 11-year-old patient. (a) Axial image, (b) parasagittal reformatted CBCT images, and (c) panoramic image show an amorphous radiopaque lesion within the left upper jaw around
the crown of tooth 24 (arrows), surrounded by a lucent follicle (arrowheads) formed
by a fibrous capsule.
The size of the lesions may range between 1 and 3 cm.[19] The posterior mandible and ramus is most commonly involved in complex odontoma,
whereas a compound odontoma is most common in the anterior maxilla.[3]
[4]
[15] Lesions may have a mass effect causing impaction, malpositioning, and resorption
of adjacent teeth.[1]
[2]
[20]
Surgical excision is the treatment of choice. Recurrence is rare.[19]
Adenomatoid Odontogenic Tumor
This adenomatoid odontogenic tumor was formerly known as odonto-ameloblastoma.[21] It may be located around the crown of the tooth or without any relation to the tooth.
It is most frequently located in the anterior maxilla in the second decade of life
and predominantly in female patients.[2]
Radiographically and on CBCT, it is primarily of mixed density consisting of a well-delineated
radiolucent lesion with intralesional flecks of calcifications with a “faint snowflake”
or “small pebble” appearance. Most of the lesions are associated with an impacted
tooth that is completely contained within the lesion, in contrast with a dentigerous
cyst that typically attaches at the cementoenamel junction.[2]
Calcifying Epithelial Odontogenic Tumor
Calcifying epithelial odontogenic tumor (CEOT), or Pindborg tumor, is a rare odontogenic
neoplasm originating from odontogenic epithelium. It can occur at any age, but it
is most common in the fifth decade. The posterior mandible is most often involved
with predilection of the first and second molars.[10]
[22]
[23] It may be located either around the crown of the tooth or is not tooth related.[2]
On radiographs and CBCT, the lesion has a variable density ranging from radiolucent,
mixed radiolucent-radiopaque, to dense radiopaque.[24] Clustered intralesional calcifications are typically seen around the tooth crown,
and the lesion is often associated with impaction of one or multiple teeth.[24] CEOT may be either well defined or ill-defined and may have a unilocular or multilocular
appearance.
Dentinogenic Ghost Cell Tumor
Dentinogenic ghost cell tumor (DGCT) is considered a rare neoplastic variant of CEOT.[25] There are two distinct types of DGCT. The intraosseous DGCT tends to be locally aggressive with a mean age of 40 years. It mainly occurs in the
canine to first molar region, usually presents as a painless bony swelling, although
slight numbness and pain may occur as well. The extraosseous DGCT, in contrast, exhibits limited growth potential and usually occurs in the sixth decade.[26] The anterior regions of the jawbones are usually affected, typically at edentulous
areas. Clinically, a firm painless nodule on the gingival or alveolar mucosa is seen.[27]
Radiographically and on CBCT, a variable appearance may be seen. Although the lesion
is most often of mixed density with a variable degree of calcification, it can also
present as a completely radiolucent lesion. Most cases are unilocular, but multilocular
lesions may be observed as well. These tumors are typically well defined, often expansile,
and may result in resorption and divergence of roots of adjacent teeth.[27]
Lesions with a Specific Location
Lesions with a Specific Location
A torus is a localized outgrowth of cortical bone arising at a specific location of
the mandible or maxilla. The pathogenesis is unknown.[13] Tori are usually asymptomatic or may interfere with fitting of a dental prosthesis.
They may become symptomatic following trauma.[4]
Torus Mandibularis
A torus mandibularis ([Fig. 7] and [Fig. S3]) typically arises from the lingual surface of the mandible above the origin of the
mylohyoid muscle. The lesion is usually bilateral and may vary in size and morphology,
ranging from flat, nodular, or slightly pedunculated.[2]
[13]
Fig. 7 Torus mandibularis. Axial reformatted dental CT image shows a lobulated radiopaque
outgrowth at the lingual aspect of the right and left mandible (arrows).
Torus mandibularis should not be confused with genial tubercles that are prominent
insertional spines at the mandibular insertion of the geniohyoid and genioglossus
muscles.[2]
Torus Palatinus
A torus palatinus ([Fig. 8] and [Fig. S4]) is a similar nodular bony overgrowth at the midline of the hard palate.[2]
[15]
Fig. 8 Torus palatinus. Coronal reformatted dental CT image shows a paramedian bilateral
radiopaque outgrowth at the hard palate (arrow).
Torus Maxillaris
A torus maxillaris arises at the lingual surface of the posterior maxilla.[4]
Lesions That May Not Have Contact with Teeth
Lesions That May Not Have Contact with Teeth
Odontoma
Odontoma may occasionally show no contact with the teeth on imaging. For further detailed
discussion of the imaging appearance of odontoma, see the earlier discussion.
Bone Island
Dense bone islands, or enostomas, are common incidental findings, consisting of failure
of resorption of secondary spongiosa within the trabecular bone.[15] Any bone, including the jawbones, may be affected.
Radiologically and on CBCT ([Fig. 9]), the sclerotic focus typically has peripheral thorny radiations, blending with
the trabeculae of the surrounding spongiosa. The shape may be round, oval, or oblong.
Fig. 9 Bone island. (a) Axial and (b) panoramic reformatted images showing a dense bone island with spicular margins within
the right mandible (arrows). The lesion has no relationship with a tooth. It should
be differentiated from sclerosing (condensing) osteitis that represents a chronic
inflammation usually around the apex of a tooth. In the latter, there is often associated
widening of the periodontal ligament around the tooth.
The lesion should not be confused with an osteoblastic metastasis. The presence of
spicular borders argues against osteoblastic metastasis. In addition, attenuation
measurements on CT may also be useful to distinguish untreated osteoblastic metastases
from enostomas in patients with a history of a primary malignancy. A mean attenuation
of 885 HU and a maximum attenuation of 1,060 HU provide reliable thresholds below
which a metastatic lesion is the favored diagnosis.[15] On magnetic resonance imaging (MRI), the lesion is typically of low signal on all
pulse sequences. Most bone islands do not grow and do not demonstrate scintigraphic
activity.[15]
Osteoma
Osteomas are benign tumors composed of mature compact or cancellous bone and mostly
arise in the craniofacial bones ([Fig. S5]), with the posterior mandibular body or condyle the most common.[4] Bone expansion may be seen. Multiple osteomas are associated with Gardner's syndrome.[4]
Osteomas are further discussed in the article “Fibrous Dysplasia, Paget's Disease,
and Uncommon Bone Lesions of the Craniofacial Bones.”
Chronic Osteomyelitis
Chronic osteomyelitis of the jawbones results from either a persistent infection due
to inadequately treated acute infection or a long-term low-grade infection.[2]
[15] There are three types of chronic osteomyelitis of the jaws.
The first type, chronic sclerosing osteomyelitis, has a predominant sclerotic component that may be either diffuse or focal. The focal
subtype is also designated as periapical osteitis or condensing osteitis and presents
radiographically and on CBCT ([Fig. S6]) as a well-circumscribed periapical radiopaque lesion (see earlier).[2]
[15] The diffuse subtype is less frequent and characterized by diffuse endosteal sclerosis
on radiographs and CBCT.[2]
Chronic suppurative osteomyelitis ([Fig. 10]) is the second subtype and characterized radiologically by a mixture of bone destruction,
sequestrum, and extensive involucrum formation.[2]
[15] Inflammation into the adjacent soft tissue may cause myositis, abscess formation,
and sinus tracts.[2]
Fig. 10 Chronic suppurative osteomyelitis. (a) Axial CBCT image shows a mixture of bone destruction with intralesional sequestrum
(thin arrow) and extensive periosteal reaction (involucrum) at the buccal and lingual
cortex of the right mandible (arrows). (b) Sagittal reformatted CBCT image shows extensive periosteal reaction (involucrum)
(arrows) and a sinus tract to the buccal cortex (arrowhead).
Fig. 11 Osteomyelitis with proliferative periostitis of Garré in a 12-year-old boy. (a) Axial CT image shows sclerosis of the left mandible and marked periosteal reaction
of the buccal and lingual cortex (arrows). (b) Oblique sagittal reformatted CBCT image shows inhomogeneous sclerosis of the mandible
(arrowhead).
The third type is osteomyelitis with proliferative periostitis or Garré osteomyelitis ([Fig. 11]). It is typically seen in children and adolescents. On radiographs and on CBCT,
there is a multilamellar periosteal reaction, with an onion peel appearance, most
often located at the inferior, buccal, and lingual aspect of the mandible.[2]
[15]
Osteoradionecrosis
Osteoradionecrosis of the jawbones may develop after radiation therapy for head and
neck tumors receiving a dose > 60 Gy.[15] It usually occurs between 4 months and 3 years following radiotherapy.[15] It most commonly affects the body of the mandible, with typical sparing of the chin
and the angles, presumably because of its muscular insertions.[4] The buccal cortex is more vulnerable than the lingual cortex.[4]
On radiograph and CBCT ([Fig. 12] and [Fig. S7]), osteoradionecrosis exhibits a mixed lytic and sclerotic appearance, with areas
of fragmentation or sequestration. Intralesional gas may be seen as well and strongly
supports the diagnosis of osteoradionecrosis.[1]
[13]
[28]
[29]
Fig. 12 Osteoradionecrosis. Axial CT image shows irregular delineated bone destruction with
cortical breakthrough of the buccal and lingual cortex of the left mandible (pathologic
fracture) (arrows). Note subtle intralesional gas and sequestrum formation.
The lesion may mimic tumor recurrence.[30] The presence of buccal erosions and involvement of the contralateral side of the
mandible are important clues to the diagnosis of osteoradionecrosis.[31]
[32] Diffusion-weighted MRI may be used to differentiate tumor recurrence from osteoradionecrosis.
High apparent diffusion coefficient (ADC) values are seen in necrosis, whereas low
ADC values are seen in recurrent tumor.[33]
Bisphosphonate-related Osteonecrosis
Bisphosphonate-related osteonecrosis of the jaws (BRONJ) represents bone necrosis
secondary to bisphosphonate treatment, a drug used to treat a variety of diseases
including osteoporosis, multiple myeloma, metastatic disease, and Paget's disease
of bone.[13]
[29] Concurrent steroid treatment may further increase the risk for BRONJ.[4]
BRONJ commonly involves the mandible most often at the mylohyoid line.[4] The maxilla is less frequently involved because of its richer blood supply.[4] It may occur spontaneously or may be precipitated by tooth extraction or dental
surgery.[4]
[33] Clinical presentation is usually painful but may be asymptomatic as well.[4]
On radiographs and CBCT ([Fig. 13] and [Fig. S8]), a mixture of bone sclerosis and osteolysis is seen. Periosteal reaction, fistula
formation, and pathologic fracture may occur in long-standing disease.[34]
Fig. 13 Bisphosphonate-related osteonecrosis of the jaws. (a) Lateral view of the skull shows multiple punched-out lesions in a patient with multiple
myeloma that was therefore treated by bisphosphonates. (b) Sagittal reformatted CBCT image shows an ill-defined area of mixed density in the
right mandible (arrow).
(Osteo)chondroma
Enchondroma originate from cartilaginous remnants in the bone. Compared with their occurrence
in the long bones, they are rare in the jawbones. Radiographically and on CBCT, the
lesion may be radiolucent with typical intralesional popcorn or ring-and-arc chondroid-like
calcification. On MRI, they have a typical cartilaginous matrix, which is of high
signal on T2-weighted images and show a ring-and-arc enhancement pattern after intravenous
administration of gadolinium contrast. Morphologically, the lesions have a multilobular
appearance.
Osteochondroma or cartilaginous exostosis are also rarely seen at the craniofacial bones.[35] These tumors have a predilection for the coronoid and condylar processes of the
mandible[2] that may exhibit a focal mushroom-shaped enlargement. Osteochondroma are usually
solitary but may be part of hereditary multiple exostosis syndrome (HMES). However,
involvement of the mandible has only been exceptionally reported in association with
HMES.[35]
[36]
Small lesions may be asymptomatic, but larger lesions may cause a decreased mouth
opening. Continuity of the cortex and the medullary bone of the lesion and the underlying
host bone is a characteristic imaging finding on plain radiographs and CT ([Fig. 14]). The surface is typically covered by a cartilaginous cap that is of high signal
intensity on T2-weighted images. The thickness of the cartilage cap is an important
parameter to differentiate benign osteochondroma from chondrosarcomas and should not
exceed 2 cm in benign osteochondroma. If thicker, malignancy should be suspected.
Although malignant degeneration is a rare occurrence in solitary osteochondroma, it
is much more frequent in HMES.[36]
[37]
Fig. 14 Osteochondroma of the mandible. (a) Axial and (b) coronal CT image shows a mushroom-shaped radiopaque lesion at the right mandibular
angle. Note continuity of the cortical and trabecular bone of the lesion and the mandible
(arrows).
Osteoblastic Metastasis
Osteoblastic metastasis rarely occurs in the jawbones and is predominantly seen in
prostate carcinoma, although other primary carcinomas (e.g., breast, thyroid, kidney)
may also have a mixed or osteoblastic appearance. Approximately 80 to 85% of metastases
involve the mandible, most commonly the molar region.[11]
[38]
[39] Compared with osteosarcoma, an aggressive periosteal reaction is rare in osteoblastic
metastasis ([Fig. 15] and [Fig. S9]) but may occur, resulting in a pseudosarcomatous imaging appearance.
Fig. 15 Osteoblastic metastasis of a breast carcinoma. Axial CT shows an osteoblastic bone
lesion in the left mandible with aggressive hair-on-end periosteal reaction (arrowheads)
and soft tissue extension (arrow). This type of periosteal reaction may also be seen
in a gnathic osteosarcoma.
Osteosarcoma
Osteosarcoma of the jawbones or gnathic osteosarcomas account for up to 10% of all
osteosarcomas.[2]
[13] They tend to occur in an older age group usually between 30 and 39 years and have
an overall better prognosis than conventional osteosarcoma.[13]
[40]
[41] Risk factors include prior radiation therapy of the head and neck region and Paget's
disease of bone.[13]
Early stage gnathic osteosarcoma may be osteolytic, causing widening of the periodontal
ligament or irregular and indistinct lining of the mandibular canal.[2]
[15] Osteolytic lesions may cause bone resorption around the roots of teeth, causing
a floating or hanging tooth appearance.[2] More advanced lesions ([Fig. 16]) are typically osteoblastic or most commonly mixed on radiographs and CBCT, due
to the presence of mineralized osteoid matrix.[2]
Fig. 16 Osteosarcoma of the left maxillary sinus. Axial dental CT shows opacification of
the left maxillary sinus with intralesional calcification (arrow) and hair-on-end
periosteal reaction in the left fossa infratemporalis (arrowheads). Reprinted with
permission from JBSR.
These lesions are typically destructive with poorly defined margins, cortex destruction,
and aggressive periosteal reaction (hair-on-end or sunray type) in 25% of cases.[2]
[13] CBCT is the preferred modality to detect the presence of osteoid matrix, whereas
MRI is the modality of choice for local staging, evaluation of bone marrow, and soft
tissue involvement ([Fig. S10]).[40]
Odontogenic Myxoma/Myxofibroma
Odontogenic myxoma/myxofibromas are rare odontogenic lesions occurring in the second
to fourth decade of life.[15] The lesions are benign but may be locally aggressive causing cortical destruction
and resorption of adjacent teeth on radiographs and CBCT. Lesions are well defined
or ill-defined and may be unilocular or multilocular. Intralesional trabeculations
may result in a honeycomb or tennis-racket appearance on radiographs ([Fig. 17]). The lesions may have a mixed density due to irregular intralesional calcifications.[17]
Fig. 17 Odontogenic myxoma. Axial CBCT shows an osteolytic lesion of the right mandible with
intralesional trabeculations resulting in a honeycomb appearance (arrow).
Osteoid Osteoma and Osteoblastoma
Although osteoid osteoma is a common benign bone tumor, it only rarely affects the
jawbones, with the posterior mandible the most frequently involved. It is often painful,
most pronounced at night, and mitigated by treatment with salicylates.
On radiographs and CBCT, the lesion shows a radiolucent nidus (often with a central
calcification), surrounded by extensive sclerosis.[42] On MRI, the lesion is surrounded by extensive bone and soft tissue edema, but the
small nidus is often less visible than on CBCT.
Osteoblastoma is regarded as a giant osteoid osteoma. It also rarely affects the craniofacial
bones, with a similar predilection as osteoid osteoma for the posterior mandible.
It affects young patients with a mean age < 20 years.
Radiologically, the lesion is usually ill-defined and radiolucent or of mixed opacity,
often with sclerotic margins and intralesional calcifications.[33] On MRI, the lesion shows marked enhancement.[33]
Calcifying (Epithelial) Odontogenic Cyst
The calcifying odontogenic cyst ([Fig. S11]) is also known as keratinizing and calcifying ameloblastoma, keratinizing and calcifying
odontogenic cyst, or Gorlin cyst.[43] The lesion may present either as a unilocular radiolucency or as a lesion with a
mixed radiolucent/radiopaque appearance.[44]
Fibrous Dysplasia and Paget's Disease
Fibrous dysplasia and Paget's disease are discussed further in the article “Fibrous
Dysplasia, Paget's Disease, and Uncommon Bone Lesions of the Craniofacial Bones” in
this issue.
Conclusion
The combination of clinical presentation, age, lesion distribution, and imaging findings
are the cornerstones for appropriate lesion characterization of most radiopaque lesions
and lesions of mixed density of the jaws. This is pivotal for defining further lesion
management. Indeterminate lesions should be referred for biopsy and subsequent histopathologic
examination. It is of utmost importance that interpretation of histopathologic specimens
be correlated with clinical and radiologic examinations to obtain a correct definitive
diagnosis.
