Oral Cavity: The Jaw and Teeth
Diagnosis | Findings | Comments |
Periodontal/radicular cyst/periapical cyst | Radiograph (panorex): well-circumscribed radiolucency around apex of tooth surrounded by thin rim of cortical bone. | Most common cyst. Associated with carious teeth. If large may displace teeth. |
Dentigerous/follicular cyst | Plain radiograph/panorex/CT: well-defined unilocular cyst, which incorporates the crown of the unerrupted tooth. | Vary in size. More common in mandible. If maxillary, may project into antrum. |
Odontogenic keratocyst/primordial cyst Multiple indicates Gorlin syndrome | Radiograph/CT: expansile cystic lesion, uni-multiloculated, smooth/scalloped border, ± impacted tooth. | Characteristically in body/ramus of mandible. Often recurs. Aggressive. |
Residual cyst | A cyst that remains or develops after surgical removal of a tooth. |
Diagnosis | Findings | Comments |
Fissural cyst | Radiograph/panorex: round or ovoid midline cyst near anterior palatine papilla. | Unusual in children. Developmental cyst in incisive canal. Often incidental. |
Aneurysmal bone cyst | Radiograph/panorex: large, multiloculated. CT: cystic, expansile, multiple fluid-fluid levels. | More common in females. Rapidly growing, painless. |
Giant cell granuloma | Plain radiograph/CT: Expansile, multilocular radiolu-cent lytic lesion with tiny bone septa traversing lesion. Contains intralesional mineralization. Enhances postcontrast. MRI: T1 and T2 hypointense, enhances postcontrast. | Rare, benign, slow-growing lesion in mandible/maxilla. Present with swelling and pain. Teeth and root displacement occurs. |
LCH | Radiograph/CT: Lytic destructive bone lesion with resorption of lamina dura resulting in floating teeth appearance. Associated heterogeneously enhancing soft-tissue mass. MRI: T1 iso-/hypointense mass, T2 hyperintense, variable CE. | |
Hemangioma | Radiograph/CT: Radiolucent area traversed by t rabeculae forming various sized cavities. If trabeculae arranged in radiating pattern, then sunburst appearance. | Rare. Rapid proliferation phase followed by slower involution phase. |
Metastasis | Radiograph/CT: fairly well-defined, lytic mass with soft-tissue component. | |
Bone cyst due to trauma/injury | Radiograph/panorex: slightly irregular cyst with poorly defined borders and scalloped margins between the roots. | Often incidental. May regress spontaneously. |
Fibrous dysplasia | CT: Depends on fibrous vs osseous component. Varies from radiolucent to ground-glass. Uni-/multilocular lesion, well-defined margin. MRI: sharply demarcated mass, variable signal intensity, diffuse CE. | |
Pain, swelling, and displacement of teeth. Active growth in childhood. Malignant transformation in polyostotic variant described. |
Diagnosis | Findings | Comments |
Burkitt lymphoma | Radiograph: Poorly-defined destructive, mottled bone lesion with root resorption and loss of lamina dura of developing teeth. Associated cortical loss. CT: destructive soft-tissue mass with extension into surrounding soft tissue. MRI: diffuse infiltration, heterogenous mass with CE. | African variant most common childhood malignancy in Africa. African Burkitt strongly associated with Epstein-Barr virus (EBV). |
LCH Fig. 4.150, p. 387 | Radiograph/CT: Lytic destructive bone lesion with resorption of lamina dura resulting in floating tooth appearance. Associated heterogeneously enhancing soft-tissue mass. MRI: T1 iso-/hypointense mass, T2 hyperintense, variable CE. | |
Osteosarcoma | Radiograph/CT: lytic bone destruction with ill-defined margins (osteolytic type) or areas of sclerosis (o steoblastic type) with aggressive periosteal reaction, ± sunburst effect, ± cortical breakthrough, and ± calcification/osteoid formation. MRI: heterogeneous mass. NM: increased uptake, identifies other bone lesions. | Prone to recurrence and metastases. |
Rhabdomyosarcoma | CT: Soft-tissue mass with variable but diffuse CE, ± bone erosion. May extend to involve mandible depending on site. MRI: T1 isointense, T2 hyperintense, variable but diffuse CE. | Forty percent occur in head and neck. May extend intracranially. |
Leukemia | Radiograph/CT: loss of lamina dura, varying degree of lytic bone destruction. | |
Odontoma | Radiograph/panorex: initially radiolucent then calcified, with the calcified portion separated from expanded cortex by a radiolucent zone ± impacted, unerrupted tooth. | Benign tumor made up of various components of teeth (enamel, dentin, cementum, pulp). Located between roots of teeth. May be associated with unerupted tooth. |
Metastasis | Radiograph/CT: fairly well-defined, lytic mass with soft-tissue component. | |
Cementoma: cementifying fibroma | Radiograph/panorex: Early—well-circumscribed, well-demarcated radiolucent lesion with no internal radiopacities. Late—contains internal radiopacities. | Slow growing: 1–2 cm. |
Benign cementoblastoma (true cementoma) | Well-defined, dense radiopaque material attached to tooth root with surrounding radiolucent zone. | Rare. Mandibular first molar most frequently involved. |
Diagnosis | Findings | Comments |
LCH Fig. 4.150, p. 387 | Radiograph/CT: Lytic destructive bone lesion with resorption of lamina dura resulting in floating tooth appearance. Associated heterogeneously enhancing soft-tissue mass. MRI: T1 iso-/hypointense mass, T2 hyperintense, variable CE. | |
Metastasis | Radiograph/CT: aggressive bone destruction, no periosteal reaction/calcification. | |
Leukemia | Radiograph/CT: loss of lamina dura, varying degree lytic bone destruction. CT: permeative bone destruction. MR: T1—leukemic infiltrate of low signal replacing normal fatty marrow. T2—increased signal. | |
Burkitt lymphoma | Radiograph: Poorly defined destructive, mottled bone lesion with root resorption and loss of lamina dura of developing teeth. Associated cortical loss. CT: destructive soft-tissue mass with extension into surrounding soft tissue. MRI: diffuse infiltration, heterogenous mass with CE. | African variant most common childhood malignancy in Africa. African Burkitt strongly associated with EBV. |
Desmoplastic fibroma | Radiograph/CT: destructive, expansile mass, contains lacelike calcification. | Aggressive, high recurrence rate. |
Diagnosis | Findings | Comments |
Osteomyelitis | Radiograph: sclerosis or mixed sclerotic/lucent. | Primary chronic osteomyelitis: nonsuppurative, noninfectious. Actinimycosis occurs in mandible. |
Infantile cortical hyperostosis (Caffey disease) Fig. 4.155, p. 390 | Radiograph: periosteal thickening, dense laminated subperiosteal new bone formation of mandible, may cause mandibular asymmetry. | |
Fibrous dysplasia Fig. 4.151, p. 387 | CT: Depends on fibrous vs. osseous component. Varies from radiolucent to ground-glass. Uni-/multilocular lesion, well-defined margin. MRI: sharply demarcated mass, variable signal intensity, diffuse CE. | |
Camurati-Engelmann disease | Radiograph: sclerosis of base of the skull (BOS) ± cranial vault and facial bones. | |
Van Buchem disease | Radiograph: osteosclerosis and hyperostosis of mandible, endosteal sclerosis of cranium. |
Diagnosis | Findings | Comments |
Down syndrome | Radiograph: hypoplasia of the facial bones and sinuses, short hard palate, hypotelorism, dental abnormalities (delayed tooth eruption, anodontia). | |
Pierre Robin syndrome | Radiograph: mandible hypoplasia, obtuse mandibular angle, cleft palate. | |
Alcohol embryopathy | Radiograph: mandible hypoplasia, microcephaly. | Growth retardation. |
DiGeorge syndrome | Radiograph: mandible hypoplasia, hypertelorism. Thymic aplasia. | |
Crouzon syndrome | Radiograph: premature closure any/all sutures, hypoplasia of the maxillomalar facial mass, recession malar bone, short and distorted zygomatic arches. | |
MPS (Hurler syndrome) | Radiograph: short wide mandible with obtuse angle, short rami, and flat/concave condyles. Premature closure of sutures, thickened calvarium at base, J-shaped sella. | |
Mandibulofacial dysostosis | Radiograph: hypoplasia/agenesis of malar bones, cleft palate. | Abnormality of first and second pharyngeal pouch, groove and arch structures. |
Seckel syndrome | Radiograph: hypoplasia maxilla and mandible, microcrania, hypertelorism. | “Bird-headed appearance.” |
Acrofacial dysostosis | Radiograph: mandible hypoplasia, craniosynostosis. | |
Melnick-Needles syndrome | Radiograph: mandible hypoplasia, BOS sclerosis. | |
Goldenhar syndrome | Radiograph: hypoplasia maxilla ± mandible and temporal bones. | Usually unilateral. |
Caffey disease | Radiograph: periosteal thickening and dense, laminated, subperiosteal new bone formation of mandible causing mandibular asymmetry. | Mandible, clavicles, and ribs most commonly involved. |
Trisomy 13/15 | Radiograph: mandible hypoplasia. | |
Trisomy 17/18 | Radiograph: mandible and maxilla hypoplasia, J-shaped sella, thin calvaria. | |
Pyknodysostosis | Radiograph: mandible hypoplasia, obtuse or absent angle of mandible, wormian bones, dental abnormalities. | Generalized osteosclerosis. |
Hallermann-Streiff syndrome | Radiograph: mandible hypoplasia, anterior displacement of temporomandibular joint, brachycephaly. | |
Campomelic dysplasia | Radiograph: mandible hypoplasia, antegonal notching of mandible, macrocephaly. | |
Metaphyseal chondrodysplasia (Jansen type) | Radiograph: mandible hypoplasia with irregular mineralization, brachycephaly, platybasia. | |
Russell-Silver syndrome | Radiograph: mandible hypoplasia. | Two-thirds have partial or total asymmetry of face, small triangular face. |
Rubenstein-Taybi syndrome | Radiograph: mild retrognathia, mandible hypoplasia, cleft palate. |