Abstract
Introduction
The radiology of the most important and/or frequent lesions affecting the bones of the face and jaws has been set out in this review and pictorial essay.
Methods
The latter is composed of multiple images displaying one or more key radiological features derived from almost every one of the most important and/ or frequent lesion affecting the face and the jaws. These images have been grouped together in 18 figures, each served by a detailed and free-standing legend. These lesions are outlined in a flowchart, which focuses on one or at most two radiological features in turn.
Results
It begins with those lesions that could indicate systemic disease, such as multiple lesions, and then proceeds onward to single lesions. The first of these single lesions are the neoplasms which need not only an early diagnosis, but also complete ablation in the majority of cases. Cystic lesions are then next, including consideration of the frequently occurring non-cysts such as simple bone cysts and lingual bone defects which require no treatment. Finally, it ends with the periapical radiolucency of inflammatory origin.
Conclusion
The most important and/or frequent lesions affecting the bones of the face and jaws that present to the oral and maxillofacial clinician can be considered systematically en route to the ‘periapical radiolucency of inflammatory origin,’ which is one of the most usually encountered lesions in clinical dentistry.
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Introduction
It is the purpose of this paper to review the radiological presentation of the most frequent and/or important lesions affecting the bones of the face and the jaws. These are set out in Fig. 1. The calcified carotid artery atheroma and its differential diagnosis of radiopacities presenting in the soft tissues of the neck have been already fully addressed elsewhere [1]. Although a three-dimensional (3D) perception of the anatomy and lesion by conventional radiography (CR) is limited, the vast majority of lesions are diagnosed by CR alone. CR is also superior to any advanced imaging modality due to its ease of access, low-cost, relatively very low radiation dose, and superior spatial resolution. Furthermore, the conventional panoramic radiograph will display the entire jaws optimally exhibiting the site and extent of lesions, such as that of systemic sclerosis (scleroderma) in Fig. 2a [2]. Since CR of the most important and/or frequent lesions affecting the face and jaws has been fully addressed in the standard radiology textbooks, the limited space in this paper will be dedicated to cross-sectional imaging, substantially derived from cone-beam computed tomography (CBCT). These will reveal a perspective of these lesions hitherto not obvious on two-dimensional (2D) CR images alone. CBCT also enhances pre-surgical planning of cysts and benign neoplasms of up to four dental units [3]. Lesions of this size can be effectively treated in out-patient facilities. Larger lesions are better treated in an in-patient hospital setting, where medical CT [now almost always multidetector CT (MDCT)] and/or MRI are widely available. Asaumi and co-workers have revealed that the roles magnetic resonance imaging (MRI) can play in the differentiation between different lesions [4].
Although periapical radiolucencies of inflammatory origin (PRIOs) [6] are the most frequent lesions that present in dentistry there are many other lesions that should be considered first. The text will follow the flowchart in Fig. 1 by first addressing those lesions likely of systemic origin.
Multiple lesions within the jaw bones
Figure 1 begins at the very top with multiple discrete lesions. Such lesions are generally underpinned by a systemic disease process, and thus caution the primary care dentist, particularly those in general or family dentistry’ that the treatment they deliver will be limited in scope and that the patient may need to be considered for referral to an appropriate specialist. Osteoporosis is generally osteolytic, and therefore, the jaws present radiologically more translucent. Although the OSTEODENT index predicts probability of a hip fracture caused by osteoporosis derived in part from a panoramic radiograph prospective trials are needed to confirm this finding and to determine its practicability in clinical dental practice [7].
Lesions may create changes in the jaws from outside or within the jaws. Scleroderma is an important example of the former resulting in the disappearance of the normal anatomical elements of the mandible, such the condylar and coronoid processes, angles, and parts of the ramus (Fig. 2a) [2]. Although most other changes are radiolucencies, the malignant transformation in the polyposis coli of Gardner’s syndrome may be preceded by multiple osteomas in the jaws and other facial bones (Fig. 2b, c) [5].
Multiple radiolucencies particularly in the young may prompt consideration of cherubism (Fig. 3a) and multiple keratocystic odontogenic cysts (KCOT; also called ‘odontogenic keratocysts’), suggestive of nevoid basal cell carcinoma syndrome (NBCCS; formerly called ‘Gorlin–Goltz syndrome’) (Fig. 3b–d) [8, 9]. This syndrome requires multi-disciplinary management, embracing many dental and medical specialties. Another cause is cherubism (Fig. 3a) [10]. Although the cherubism proband classically presents with bilateral and bimaxillary multilocular radiolucencies mainly in the posterior sextants, other family members of the proband upon investigation frequently present with atypical lesions, such as radiolucencies in the midline of the mandible [6]. The lesions in cherubism can cause ocular and respiratory problems, generally in the early stages. The latter is due to obstruction of the airway resulting from a backward displacement of the tongue or to an obstruction of the nasal passages. Lymphadenopathy may also occur in the early stages [10].
The degree of marginal definition or ‘zone of transition’ (as frequently called by medical radiologists) is the most important feature of a lesion presenting on CR. A lesion on a CR with a zone of transition 1 mm or less will appear well-defined, whereas as those greater will appear poorly defined (Fig. 4a) [11]. The latter presentation prompts consideration of a malignant or an infected lesion; the distinction is often provisionally made with regard to the lesion’s clinical presentation. A radiopaque lesion with a poorly defined margin on CR could be fibrous dysplasia (Fig. 4a) or sclerosing osteomyelitis (Fig. 6b). In those cases affecting the body of the mandible, the outline of the mandibular canal is enhanced by either lesion. This enhancement is due to the investment of the mandibular canal by dysplastic bone or osteosclerosis, respectively [11].
Polyostotic fibrous dysplasia manifests in the young patient (Fig. 4), with McCune–Albright syndrome presenting in the infant [12]. Fibrous dysplasia arising within the jaw bones presents on CR as a poorly defined lesion, observed on CR (Fig. 4a, b), whereas fibrous dysplasia arising elsewhere, namely, the appendicular skeleton, is usually well-defined. It should be noted that the poorer defined margins of fibrous dysplasia of the jaw on CR were not noted in MDCT reflecting the poorer spatial resolution of the latter (Fig. 4c–e) [13]. Nevertheless, the poorer defined margins may also be appreciated on CBCT when a higher spatial resolution is used; see both cases in Fig. 5. The difference between the gnathic and appendicular cases of fibrous dysplasia may reflect the fact that the bones of the jaws developed in membrane, whereas the most of appendicular skeleton developed by endochondral ossification. This supposition is supported by the presence of cartilage in fibrous dysplasia affecting the appendicular skeleton, but absent in those affecting the jaws [12].
This leads onto the monostotic fibrous dysplasia affecting the face and jaws. This accounts for well over 90% of all such cases of fibrous dysplasia [12]. Figure 5 displays CBCTs of two such cases 5a and b affecting the mandible and 5c and d affecting the maxilla. Typically, only one side of the jaw is affected by fibrous dysplasia. Figure 5a, b displays a lack of lamina dura associated with tooth roots invested by dysplastic bone. Figure 5c, d exhibits the obturation of the maxillary sinus which was also noted in Fig. 4c–e. They are the two more important diagnostic features of fibrous dysplasia affecting the face and jaws. Figure 5c, d displays the sharply defined demarcation between a completely dysplastic bone, here the maxillary bone, and the adjacent normal bone, the zygomatic or malar bone precisely at the zygomatico-maxillary suture in a monostotic case, in comparison with Fig. 4c–e, a polyostotic case in which these contiguous bones are both dysplastic.
Other diseases with multiple lesions affecting the jaws are florid osseous dysplasia and periapical osseous dysplasia. Since these are generally not accompanied by other lesions elsewhere in the body, they will be addressed in the next section addressing ‘other radiopaque lesions’.
Other radiopaque lesions
Other radiopaque lesions that have poorly defined margins like fibrous dysplasia are sclerosing osteomyelitis (Fig. 6b) and medication-related osteonecrosis of the jaws (MRONJ) (Fig. 7). Although both sclerosing osteomyelitis and MRONJ can display a zone of sclerosis (increased radiopacity) extending outside the alveolus into adjacent basal bone, some buccolingual expansion (due to new bone formation) and a sequestrum (an island of dead bone), all three are generally viewed together in MRONJ. The MRONJ can arise when antiresorptive agents, such as bisphosphonates and denosumab, were used to treat osteoporosis or oncology patients [14]. A long term Japanese study reported that although bisphosphonates delay tooth-socket healing, they did not cause a single case of MRONJ [15]. CBCT was used to predict future bone exposure of Stage 0 MRONJ by identifying radiographic sequestration [16].
The rest of the radiopacities are well-defined. The majority is either areas of sclerosing osteitis, which occur secondary to pupal necrosis (Fig. 6b), or dense bone islands. Although the dense bone island is considered idiopathic (that is having no known cause), hence, its alternative name of idiopathic sclerosis, a relation between its size and its prevalence and the concentration of fluoride in the water were discussed in one report [20]. This report included an East Asian community [20]. Both sclerosing osteitis and dense bone islands can be further distinguished from the other well-defined radiopacities as their trabeculae are continuous with the adjacent normal bone, whereas the rest are generally separated from the adjacent bone by a capsule [11]. These encapsulated lesions are osseous dysplasias (Figs. 8, 9, 10), cementoblastomas (Fig. 6a–d), odontomas (Fig. 6e), and ossifying fibromas (OF) (Fig. 11). The only exception to this is the juvenile variants of OF (Fig. 11d, e), which do not generally display capsules. This absence of a capsule may account for their higher recurrence, due to the difficulty, during surgery, of the surgeons detecting a clear boundary between the normal adjacent tissues and the lesion [12].
Osseous dysplasia is prevalent in middle-to-old-aged females of East Asian and Sub-Saharan African origin presenting as one of two variants; the florid variant (affects more than one sextant; Figs. 8, 9) or the focal variant (a single or multiple adjacent lesions confined to a single sextant; Fig. 10) [12]. Osseous dysplastic lesions begin as radiolucencies which undergo central mineralisation (Fig. 8) [12]. Although these generally require no treatment, they pose problems if they become secondarily infected. Furthermore, their presence in the edentulous alveolus contraindicates implant placement [11]. Therefore, avoidance of these difficulties may be achieved by retention of the associated teeth. Therefore, non-vital teeth or those of questionable vitality should be referred to endodontists for treatment. In very rare cases, these lesions may expand massively necessitating ablative surgery. Reports of expanding osseous dysplasia (EOD: also called by some gigantiform cementoma) [21] are now found in all ethnicities and affect both genders. There is yet another variant, which though reported in all ethnicities, is most prevalent in young females of European origin. It is non-expanding. It is periapical osseous dysplasia (POD; formerly called periapical cemental dysplasia) [12]. POD presents initially as multiple juxtaposed periapical radiolucencies confined to the lower anterior sextant (Fig. 10). Its early radiolucent stage may occasionally prompt unnecessary endodontic treatment. Well-defined radiopacities that exhibit buccolingual expansion, root resorption and/or tooth displacement are OF (Fig. 11).
Malignant lesions
The most important feature particularly in radiolucent lesions is marginal definition or zone of transition defined earlier. A lesion presenting on CR with a zone of transition greater than 1 mm is generally considered to be either a malignant (Fig. 12) and/or an infected lesion (Fig. 13a). Although the former are the most important, the clinical examination and history generally determine the provisional diagnosis. Nevertheless, even if the lesion appears well-defined, if it displays ‘spiking’ or ‘spiked’ root resorption (Fig. 12c), ‘floating’ teeth (Fig. 12a, c) or an unexplained widening of the periodontal ligament space, then a malignant lesion should be considered. The most frequent malignancies of the face and jaws are carcinomas or non-Hodgkin lymphomas (NHL) (Fig. 12). Although both principally arise intraorally within the mucosa, the latter predominantly from the lymphoid tissue in the tonsil (lingual, palatine or pharyngeal), a minority arise within the alveolus; the carcinomas from epithelial remnants of odontogenesis (primary intraosseous squamous cell carcinoma) [11] and the NHLs from lymphocytes within the alveolus associated with dental infections in some cases [22, 23]. Kato et al. reported the advanced imaging differences between SCC and NHLs arising within the sinus [24].
Benign neoplasms
The next stage is the determination as to whether the lesion is a benign neoplasm or a cyst, because the former may recur, particularly after conservative treatment (e.g., enucleation), which is more effective for treating cystic lesions. Although a multilocular appearance (Fig. 14a, b) and/or the presence of root resorption (Fig. 14c) determine the former, their absence does not rule out consideration of a neoplasm [6]. Lesions that arise or are observed to be substantially confined to the alveolus (in the mandible above the mandibular canal, which separates the tooth-bearing alveolus and the basal process) are most likely to be odontogenic. These are either odontogenic neoplasms, such as the ameloblastoma (Fig. 14), KCOT (Fig. 15) and odontogenic myxoma (Fig. 16), or odontogenic cysts such as dentigerous cyst (Fig. 17), radicular cyst (Fig. 18a, b). Other causes are nasopalatine duct cyst (Fig. 18c, d) and/ or early stage dysplastic lesions such as osseous dysplasia (Fig. 8a) [6]. In addition to some subtypes of neoplasm such as the unicystic ameloblastoma (Fig. 14e), which have a substantial cystic component, other odontogenic neoplasms in their early stages may appear unilocular and if they secondarily envelop the crown of an unerupted tooth they need to be distinguished from the dentigerous cyst. The dentigerous cyst is attached to the enamel–cemental junction (Fig. 17a) or within a millimeter apical to it (Fig. 17c), any other relationship should be considered neoplastic. KCOTs, arising the posterior maxilla, are often observed expanding upward into the sinus lumen carrying with them an unerupted third molar. Figure 15c, d displays a KCOT, though arising in the anterior maxilla, has extended sufficiently posteriorly to exhibit a balloon-like expansion of the sinus’ anterior wall and adjacent floor (Fig. 15c) [6].
Expansion of a lesion is indicative of its nature. Almost all neoplasms and all true cysts exhibit expansion due to their centrifugal growth occasioned by cell division in the former and hydrostatic pressure in the latter. Nevertheless, there are different expansive shapes. Most neoplasms, including the ameloblastoma, and cysts exhibit a ‘beach-ball-like’ expansion (Figs. 14a, e, 17c, d, 18), whereas KCOT and odontogenic myxomas, particularly those affecting the body of the mandible (Figs. 15a, b, 16a–c), are more fusiform, as they extend more mesiodistally through the medullary cavity rather than expand buccolingually. This is due, in part, to the KCOT’s low soluble protein content and, therefore, low hydrostatic pressure in conjunction with the thick cortices of the mandible, whereas in the case of the myxoma, this is due to both the lack of a capsule and its gelatinous consistency. In the maxilla, where the cortices are thinner and are adjacent to air-filled spaces, these lesions’ expansive growth is less inhibited (Figs. 15c, d, 16d) [6].
CBCT has come to the dentist’s assistance for the diagnosis and assessment of some lesions without a need for a surgical investigation. Two such lesions that may be effectively diagnosed in this way are the lingual bone defect and some simple bone cysts (Fig. 19). The former is unique to the jaws, whereas the latter is also found elsewhere in the skeleton and is known by many names, such as traumatic bone cyst and solitary bone cyst. The lingual bone defect excavates the medullary cavity of the basal process of the mandible and in some cases erodes and displaces the buccal cortex when reached. Not only does lingual bone defect occur in middle age, so far, there has only been one published report of it causing a pathological fracture in a Japanese patient [28]. This lack of a propensity to fracture is surprising due to the considerable excavation of the body of the mandible, such as that in Fig. 19d–f. This lack of fracturing may reflect older age of onset. This older age may be associated with less of the risk-taking observed in the young. Some lingual bone defects, rather than presenting adjacent to the submandibular gland, present adjacent to the sublingual gland and, therefore, involve the premolar alveolus and need to be distinguished from other lesions; the CBCT again proves invaluable for this task.
Although the mucosal antral pseudocyst (Fig. 13b) and sinus polyps (Fig. 13c), arising within the mucosa of the maxillary sinus, outside the maxillary alveolus, are clearly displayed on panoramic radiographs [11], they still need to be excluded from pulpal necrosis in subjacent teeth, particularly if accompanied by obvious caries, large restoration/s or evidence of dental trauma. A subjacent non-vital tooth would indicate a PRIO. CBCT’s cross-sectional imaging would be indicated, where any other lesion is suspected; examples of these are Figs. 3c, d, 5c, d, 7b, 12b, 15c–f.
A PRIO (Fig. 3a, 18a, b) represents at least three separate pathological lesions the radicular cyst, the periapical granuloma and the periapical abscess. Although the granuloma is most likely to regress following optimally performed orthograde endodontics or extraction, this is not necessarily true for the radicular cyst. The latter may account for many of the persistent PRIOs observed in a nearly 30-year-long study of endodontically treated teeth [6, 11, 29].
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MacDonald, D. The most frequent and/or important lesions that affect the face and the jaws. Oral Radiol 36, 1–17 (2020). https://doi.org/10.1007/s11282-019-00367-4
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DOI: https://doi.org/10.1007/s11282-019-00367-4