References

Stafne EC. Bone cavities situated near the angle of the mandible. J Am Dent Assoc. 1942; 29:1969-1972
Turkoglu K, Orhan K. Stafne bone cavity in the anterior mandible. J Craniofac Surg. 2010; 21:1769-1775
Kim H, Seok JY, Lee S Bilateral stafne bone cavity in the anterior mandible with heterotopic salivary gland tissue: a case report. Korean J Pathol. 2014; 48:248-249
Schneider T, Filo K, Locher MC Stafne bone cavities: systematic algorithm for diagnosis derived from retrospective data over a 5-year period. Br J Oral Maxillofac Surg. 2014; 52:369-374
de Courten A, Küffer R, Samson J, Lombardi T. Anterior lingual mandibular salivary gland defect (Stafne defect) presenting as a residual cyst. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2002; 94:460-464
Falconer N, Ujam A, Siddle A, Ali N. Stafne bone cavity: the important role of MRI imaging in achieving diagnosis. Br J Oral Maxillofac Surg. 2015; 53:10-87
Bouquot JE, Gnepp DR, Dardick I, Hietanen JH. Intraosseous salivary tissue: jawbone examples of choristomas, hamartomas, embryonic rests, and inflammatory entrapment: another histogenetic source for intraosseous adenocarcinoma. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2000; 90:205-217
Sisman Y, Miloglu O, Sekerci AE, Yilmaz AB, Demirtas O, Tokmak TT. Radiographic evaluation on prevalence of Stafne bone defect: a study from two centres in Turkey. Dentomaxillofac Radiol. 2012; 41:152-158

Stafne's bone cavity – unusual presentation in the anterior mandible

From Volume 45, Issue 4, April 2018 | Pages 340-341

Authors

Ioan Davies

DCT2 Oral and Maxillofacial Surgery, St George's Hospital, Tooting, London, UK

Articles by Ioan Davies

Holly Boyes

Foundation Dentist, St Helens

Articles by Holly Boyes

James Wykes

Head and Neck Fellow, St George's Hospital, Tooting, London, UK

Articles by James Wykes

Graham Smith

(Consultant Oral and Maxillofacial Surgeon) Kingston Hospital

Articles by Graham Smith

Abstract

Abstract: Stafne's Bone Cavity (SBC) is a well described but uncommon asymptomatic pseudocyst of the mandible. Most commonly occurring in the posterior mandible, presentations anterior to the mental foramen are extremely rare and warrant thorough investigation. This case describes the presentation of a 55-year-old male with an anteriorly-positioned SBC that resembled asymptomatic dental pathology. Clinicians should be aware of SBCs as a differential diagnosis for radiolucent lesions of the mandible.

CPD/Clinical Relevance: To raise awareness of radiolucent lesions to dental professionals in both general and specialist settings.

Article

Ioan Davies

Case report

A 55-year-old male was referred to the Oral and Maxillofacial Surgery (OMFS) Department at St George's Hospital by his general dental practitioner for further investigations of an incidental finding of a radiolucency of the anterior mandible. The patient's medical history was unremarkable; he was a non-smoker and revealed no history of previous facial trauma or surgery. Initial examination revealed a moderately restored adult dentition with average oral hygiene. There was neither pain nor swelling of the buccal and lingual sulci of the mandible, and no cervical lymphadenopathy. All teeth were vital, non-mobile, not tender to percussion and no caries was identified.

An orthopantomogram (OPG) showed a well-defined, unilocular radiolucency below the apices of an unrestored and non-carious lower left first premolar (LL4). It was decided that a cone beam computed tomogram (CBCT) would be beneficial in diagnosing this lesion and in treatment planning; three-dimensional views allow an accurate assessment of size, location, and proximity to vital structures. Although not a routine imaging modality for SBC, we decided that, as we did not have a definitive diagnosis of SBC from the OPG, it would be necessary should any surgical intervention be required (Figures 1 and 2).

Figure 1. Orthopantomogram showing a unilocular radiolucent lesion inferior to the apex of the lower left first premolar.
Figure 2. Cone Beam CT showing a unilocular lesion interrupting the lingual cortex of the mandible and positioned anteriorly to the mental foramen.

The case was discussed in the OMFS radiology-pathology multidisciplinary team meeting; it was agreed that a biopsy was not warranted and the patient was discharged back to his dentist.

Literature review

Stafne's bone cavity was originally described by EC Stafne in 1942 and has a reported incidence rate of approximately 0.009% to 0.3%.1,2 The majority of cases are located between the first mandibular molar and the angle of the mandible inferior to the inferior dental canal. A review of the literature revealed under 60 reported cases in the anterior mandible.3

Usually an asymptomatic lesion, it is best described as a depression of the lingual aspect of the mandibular bone. However, its radiographic features may mimic that of an intra-bony cystic or neoplastic lesion. It is most likely to occur as a unilateral lesion in males (M:F 3:1) over the age of 50, however, bilateral cases have been reported.3,4 Specifically with regard to cases of anterior SBC, a wide range (18 to 64 years) with a mean of 43 years was noted.5

SBC is primarily identified on routine dental radiography and presents as a well-defined, unilocular, circular radiolucency; however, diagnosis with plain film alone cannot be accurately achieved.5 Cross-sectional imaging, such as CT or CBCT, are useful. MRI has been advocated due to its ability to confirm the presence of salivary gland tissue within the lesion and to limit the radiographic exposure to the patient.6

Histopathological examination is seldom necessary; however, the cavities are usually filled with normal salivary gland tissue arising from the submandibular gland. There have been reports of adipose tissue, blood vessels, skeletal muscle, fibrous connective tissue or lymphoid tissue herniating into the space.2,3

Several pathogenic theories have been suggested in relation to SBC, but the congenital malformation theory (which suggests salivary gland tissue gets entrapped within the mandible during development) is the most universally accepted.6 Lesions as a result of congenital malformation are typically associated with a thin but intact lingual cortex, but this is not consistent with our case.7 Another theory is that of adjacent structures, such as the submandibular gland compressing the lingual aspect of the mandible or local lymphatic infiltration, which may be the causative factor in our case.8

Conclusion

This is another case which highlights that SBC can present at any position along the mandible. There are multiple differential diagnoses for radiolucent lesions found on imaging. We aim to increase the awareness amongst dental practitioners as a conservative management approach is warranted. This will help to prevent unnecessary dental or surgical intervention, therefore improving care and decreasing the morbidity to patients.