A 30-year-old female patient reported to the outpatient department of Vasantdada Patil Dental College and Hospital, Sangli with a chief complaint of gingival swelling on the right maxillary posterior region. The patient noticed a painless swelling 6 months ago, which was small in size initially, started growing gradually and reached the present size. The patient revealed a history of similar swelling in the same region 2 years ago. Surgical removal of the mass had been attempted, however it had been unsuccessful due to heavy bleeding from the site. The bleeding had been controlled by cauterization.

On general examination, the patient showed unilateral port-wine stain on the right side of her face extending from the superior border of the upper lip to the bridge of the nose superoinferiorly and from the midline to the preauricular region anteroposteriorly since her birth. On clinical examination, the patient revealed about 3×3 cm sized solitary extraoral swelling on the right maxilla extending from the midline to the midpupilary line anteroposteriorly and from the superior border of the upper lip to the base of the nose superoinferiorly. The swelling was roughly ovoid in shape with diffuse borders. The overlying skin was erythematous. There was a local increase in temperature of the overlying skin. The swelling was soft in consistency and non-tender on palpation. Intraorally, about 3×6 cm sized solitary swelling, reddish pink in color was found extending from the right central incisor to the third molar on the buccal and palatal gingivae of the maxilla. The swelling involved marginal, papillary, and attached gingivae, and had smooth surface. It was soft in consistency, non-tender on palpation, compressible, pulsatile and blanched on pressure. No bleeding on palpation was noted. The right maxillary first and second premolars showed grade II mobility. The right maxillary lateral incisor was displaced laterally (Fig. 1). A provisional diagnosis of vascular lesion was given and the patient was subjected to radiographic examination. Intraoral periapical radiographs showed coarse bony trabeculae and enlarged marrow spaces on the right maxillary anterior and posterior regions. Alveolar bone loss was revealed on the maxillary central and lateral incisor regions. Widening of periodontal ligament space was seen with lateral incisor, first and second premolar and the first molar was supraerupted (Figs. 2A and B). Panoramic radiograph showed ill-defined, irregular area of bone destruction extending from the mesial surface of the left maxillary central incisor upto the mesial surface of the right maxillary canine. The maxillary central and lateral incisors showed marked displacement (Fig. 2C).

The patient was referred to The Wanless Hospital, Miraj. The ultrasound examination showed a high-flow arteriovenous malformation. Admission laboratory tests showed hemoglobin (Hb) of 7.3 g/dL, a platelet count of 63,000 per mm³, prothrombin time of 17 seconds, activated partial thromboplastin time of 35 sec, and international normalized ratio of 1.3. The patient was then given blood and platelet transfusions after which the blood investigations showed hemoglobin of 13.3 g/dL, platelet count of 1,96,000, prothrombin time 15 seconds, activated partial thromboplastin time of 28 seconds and international normalized ratio of 1.1. Diagnostic angiography was performed after gaining access from the right femoral artery. Selective catheterization of the right external carotid artery was performed under fluoroscopic guidance. The diagnostic angiogram showed a high-flow vascular malformation supplied principally by the alveolar branch of the internal maxillary artery. Surgical treatment of such lesion required extensive resection of the maxilla and might result in the dysfunction and disfigurement. Ligation of the external carotid artery was not advisable, since many anastomoses promoted the rapid appearance of a collateral circulation. Therefore, embolization which consisted of occlusion of the vessels which contributed to the lesion was considered. Further selective catheterization of the maxillary artery was performed. Embolization was performed using polyvinyl alcohol (PVA) particles (Fig. 3). The patient tolerated the procedure well and had an unremarkable postoperative course. One week postoperatively the patient showed complete regression of the palatal lesion (Fig. 4). One year follow-up revealed a significant reduction of clinical symptoms and signs of the lesion without any further complications.

AVMs are extremely rare conditions that can be fatal if left untreated.6 They are caused by disturbances in the late stages of angiogenesis, mainly abnormal differentiation of vascular system.10 Vascular malformations can be subdivided further into high-flow and low-flow lesions.1,2 In the present case, angiography was performed which demonstrated a high-flow AVM.

The diagnosis of AVMs can be made clinically in conjunction with imaging studies. Most AVMs have a history that includes the presence of a vascular blush in the overlying skin in the childhood, which begins to expand more rapidly as the patient enters puberty or undergoes other hormonal changes. They may also reveal a history of trauma to the involved area prior to the notification of the lesion. Bleeding, pain, and tissue destruction are often subsequent signs in AVM.1,6 On physical examination, early AVMs may have an overlying vascular blush in the skin similar to an early port-wine stain. The mucosa is usually thickened and vascular, and pulsation is usually present. The teeth may be loose or may exhibit pumping movement when pressure is applied and released.1,3,4,6 AVMs can invade the skin where ulcerations and bleeding are common.1,11 Some "high-flow" lesions may result in consumption coagulopathy, requiring transfusion therapy.12,13

Multiple imaging modalities should be used to evaluate characteristics of AVMs such as size, flow velocity, flow direction, relation to the surrounding structures and lesion contents.2 There are no pathognomonic radiographic features to distinguish AVMs on plain radiographs. They may appear as bone erosion, sclerotic change, periosteal reaction or a cyst like radiolucent lesion. A sunburst effect, created by spicules radiating from the center, is often present.2,14 The lesions most often have a multiloculated appearance due to residual bone trapped around vessels. Small radiolucent locules may resemble enlarged marrow spaces surrounded by coarse, dense, and well defined trabeculae. They may have a honey comb or soap-bubble pattern that is well demarcated from adjacent bone. The roots of the teeth in proximity of the lesion may show displacement or resorption. High-flow lesions tend to result in more destructive skeletal changes, appearing as moth-eaten and poorly defined areas of radiolucency.12 The radiographic differential diagnosis of these lesions include ameloblastoma, ameloblastic fiboma, odontogenic myxoma, central giant cell granuloma and metastatic malignant tumors.6

Color Doppler ultrasound examination can provide information about the flow velocity. Contrast enhanced CT can be useful in assessing the AVMs. The drawbacks of CT are considerable exposure to ionizing radiation and limited information about blood flow.2 Angiography and MR imaging are the preferred imaging modalities.2,6,10,15 MRI depicts the anatomic relation of the vascular lesion with adjacent organs and the flow velocity of lesions. It is useful for evaluating the lesions postoperatively.2 Angiography is currently the gold standard for the determination of location and flow characteristics of vascular lesions. Angiography is useful to determine blood vessels supplying blood to the lesion, and the relative venous out-flow characteristics, and the presence or absence of arteriovenous shunts.3 According to Orbach, the angiographic features of AVMs include dilatation and lengthening of afferent arteries, early and preferential filling of shunts, delayed filling of associated normal arteries, early opacification of draining veins and rapid flow to collateral vessels.16

Intentional transarterial embolization was originally described in 1969 by Lalli and coworkers.17 Treatment of vascular malformation with selective embolization procedure is currently highly recommended and often used. The purpose of the selective embolization is to abruptly cut off the blood supply of the lesion, reducing the risk of potentially massive and lethal blood loss after its rupture, enabling a more focused and selective surgical procedure with less morbidity and with maximal preservation of important structures.18 Various materials can be used for embolization. They can be classified as either temporary or permanent. Temporary materials include autologous clot or muscle, Gelfoam19,20 and microfibrillar collagen. Permanent agents include silicone spheres, lyophilized dura, PVA, isobutyl cyanoacrylate and stainless steel or platinum coils. The most commonly used materials are Gelfoam and PVA. PVA was used in present case as it is nonabsorbable and denser than Gelfoam.9

To conclude, vascular malformations represent some of the most difficult lesions to diagnose and treat. Interventional radiography plays an essential role in diagnosis and management of such lesions. With the use of this technique, extensive surgical procedures can be avoided so as to avoid facial disfigurement and functional compromise.