Recurrence of a Giant Peripheral Osteoma of Mandible

Abstract

Osteomas are rare benign tumours in the bone. We describe a case of giant osteoma involving the lingual side of the ramus and body of mandible that recurred 8 years after its surgical treatment at another hospital. Surgical resection with reconstruction is the treatment of choice for this lesion. The clinicopathological features of osteoma are discussed and Gardner’s syndrome was excluded.

Introduction

Osteomas are benign lesions composed of mature compact and/or cancellous bone that grows continuously. The pathogenesis of this tumour is currently unknown [1]. Both hamartomatous and neoplastic factors have been advocated, but no definite conclusion has been reported in any study so far.

Osteomas are of three forms: central, peripheral, or extraosseous. The central form derives from the endosteum and the peripheral form derives from the periosteum, whereas the extraosseous form develops in muscular tissue structures [2].

The most common location of the periosteal osteoma is the skull. However, lesions also occur in the mandible, especially on the lingual aspect of the body, angle and inferior border of the mandible [3].

Histologically, three types of osteoma can be identified: compact (ivory), cancellous (trabecula), and fibrous (spongy) [4].

The purpose of this article is to describe a giant osteoma involving almost half of the mandible with pain and disfigurement and complete removal of lesion by resection was the treatment option since recurrence was seen.

Case Report

A 16 year old female patient was referred to JSS Dental College and Hospital by a private dental practitioner with complaints of swelling and recurrent pain over the left posterior region of the mandible since 1 month and slowly increasing in size (Figs. 1, 2).

Fig. 1.

Pre operative lateral view

Fig. 2.

Pre operative intraoral view

Patient gave history of a swelling 8 years back in the same region where pieces of bones were surgically removed from the lingual side along with extraction of teeth on the same side in another hospital for which there was no record regarding the nature of the surgery performed.

A solitary well defined mixed radiopaque radiolucent lesion around 4 cm × 5 cm was found in the left mandibular ramus and angle region extending superiorly up to coronoid process on a orthopantomograph, mandibular left lateral view showed lingual cortical expansion (Figs. 3, 4).

Fig. 3.

Pre operative orthopantomograph

Fig. 4.

Mandibular left lateral radiograph

On palpation diffuse bony hard solitary swelling over alveolar ridge and external oblique ridge approximately 2 cm × 2 cm was noticed which was non tender on palpation with no signs of any surface mucosal changes. The lower left 2nd and 3rd molars were missing.

A single tender lymph node was palpable on the left submandibular region.

Under local anaesthesia incisional biopsy was done and histopathological study suggested cancellous osteoma.

The results of blood and serum chemistry were within the normal limits. Gardner’s syndrome was excluded in this patient as there were no relevant clinical findings as well as in ultrasound evaluation.

Informed consent was obtained preoperatively and under general anaesthesia the lesion was exposed through a left sided submandibular incision; segmental resection was done distal to left 1st premolar including the coronoid process (Fig. 5).

Fig. 5.

Intraoperative view showing resected surgical site along with preserved lingual nerve

Iliac bone graft was harvested and grafted with the help of long titanium 2.5 mm reconstruction ‘L’ plate (Fig. 6).

Fig. 6.

Intraoperative view showing placement of ‘L’ reconstruction plate with bone graft

The solitary lymph node was dissected and excised for histopathological study.

Patient underwent periodic clinical and radiographic follow-up and has remained free of tumor 3 years after surgery (Figs. 7, 8, 9, 10).

Fig. 7.

Post operative lateral view

Fig. 8.

Post operative front profile view

Fig. 9.

Post operative intraoral view

Fig. 10.

Post operative orthopantomograph

Gross Pathology

The specimen consisted of resected part of mandible about 6 cm × 6 cm × 2 cm with coronoid process. Surface showed bosellated exophytic bony growth measuring 4 × 3 cm (Figs. 11, 12).

Fig. 11.

Lingual surface of resected mandible

Fig. 12.

Buccal surface of resected mandible

Microscopic Pathology

The mass showed lamellar bone with interspersed adipose tissue and marrow elements and an impression of a cancellous osteoma was given.

The excised lymph node showed fibrocollagenous tissue suggestive of reactive lymph node hyperplasia.

Discussion

Osteomas of the maxillofacial region are often detected on routine examination except in cases where lesion is sufficiently large to cause disfigurement and or functional discomfort to the patient.

Peripheral osteomas of the maxillofacial region affects mainly the frontal bone, mandible and the paranasal sinus [4].

Cases affecting the mandible have predilection to affect the angle and condylar region followed by the molar region of the mandibular body and the ascending ramus [5–8].

The clinical, radiological and histological features of the present case support the diagnosis of peripheral cancellous osteoma of posterior lingual mandible [8].

Peripheral osteomas almost certainly arise from the periosteum and as they grow they exhibit either a pedunculated or sessile bases that are continuous with the underlying cortical bones.

Studies suggest that peripheral osteoma can be completely cured by surgical intervention, and there is no recurrence. Compact bone is made up the outer zone, covering an intermediate area of cancellous bone and showing increased osteoblastic activity. Centrally, there is a loose fibrous stroma with more vessels, plump osteoblasts, and a few trabeculae of immature bone. This zonation suggests that growth commences centrally with increasing maturation of bone toward the external surface, and it may also explain why partial excision leaving only a peripheral residuum does not usually lead to recurrence [4, 9].

Contrary to the above study our patient showed clinical recurrence following earlier complete or incomplete surgical removal of the growth.

A diagnosis of osteomas raises the possibility of Gardner’s syndrome, a condition represented by the triad of colorectal polyposis with very high propensity for malignant transformation, skeletal abnormality that include multiple osteomas of the skull and facial skeleton, and multiple supernumerary teeth [6].

Patients with Gardener’s syndrome may also present with symptoms of rectal bleeding, diarrhea and abdominal pains which was not seen in our patient.

In terms of differential diagnosis, peripheral osteomas of the jaws should be distinguished from other bony exostoses of jaws like Tori. Osteoblastoma and osteoid osteomas may present as lingual or buccal bony expansions and should be distinguished from peripheral osteomas [6].

Radiographic features of an osteoma generally show a round or oval well circumscribed radiopaque mass with a broad base [10].

In summary, although osteomas of the jaws remain a rare entity, very large lesions as in the case presented have the potential to interfere with normal function such as mouth opening, swallowing, and speech and may cause facial disfigurement and pain.

Mandibular osteoma, suspected to have Gardener’s syndrome, should be further evaluated to rule out colorectal carcinoma [11].

Malignant transformation of peripheral osteoma has not been reported in literature.

Recurrence of peripheral osteomas after surgical excision is extremely rare due to the histological zonation and increasing maturation of bone toward the external surface that is seen in these lesions [4, 9].