Implant Therapy and Apical Actinomycosis: Case Report



Treatment of periapical actinomycosis includes extraction of the involved tooth; however, indications for and timing of implant therapy remain unclear. In this case report, we describe treatment of apical actinomycosis in a 63-year-old woman following tooth extraction. After monitoring the patient for 6 months, implant therapy was carried out and remained successful after 1 year follow-up.



The long-term success rate for osseointegrated implants is high when they are used to rehabilitate fully or partially edentulous patients or for single-tooth replacement.1-3 Success of osseointegration depends mainly on the quality and quantity of the host bone bed and its healing capacity. Teeth with a history of periapical infection may be considered for replacement with endosseous implants; however, there is controversy over whether implant therapy should be delayed and several authors recommend against immediate implants in the presence of periapical or periodontal pathosis.4-6

Actinomycosis is a chronic granulomatous infectious disease characterized by suppuration, abscess formation and draining sinus tracts. Clinical and radiographic manifestations of apical actinomycosis are usually indistinguishable from common apical periodontitis.7 Actinomycotic infection slowly spreads to contiguous tissues without regard for tissue planes.8 Although nonsurgical endodontic treatment has been successful in most cases, some do not heal, even after removal of the tooth.

The most common factor associated with lack of healing is the presence of strains of Actinomyces.9 Sakellariou10 reported 47 cases where lack of periradicular healing after endodontic treatment was associated with strains of Actinomyces. A. israelii is the most common species found in periapical infections. The genus Actinomyces contains species of bacteria that are gram-positive, pleomorphic or filamentous, non-spore-forming and anaerobic or micro-aerophilic.

Other therapeutic approaches include surgical curettage supplemented by short-term antibiotic treatment, and the outcome of this treatment has been reported as favourable.11

To the best of our knowledge, this report is the first to describe implant therapy at a site with a recent history of periapical actinomycosis.

Case Report

A 63-year-old woman was referred to the graduate periodontology clinic at the faculty of dentistry, University of Manitoba, Winnipeg, Manitoba, with the main complaint of moderate, episodic pain in the area of tooth 44. An allergy to sulfanomides had been documented in her medical history.

Figure 1: Radiograph showing a periapical radiolucency associated with tooth 44 along with gutta-percha extending through the apical foramen.

The patient's periodontal record indicated satisfactory oral hygiene (modified O'Leary plaque score12 = 8%). On examination, the existing dentition in the lower sextants appeared periodontally healthy. She was wearing a complete upper denture. A panoramic radiograph revealed an overfilled root canal at the apex of tooth 44 (Fig. 1). The differential diagnosis included periapical abscess, periapical cyst and granuloma.

The tooth was extracted. At 6 months follow-up, periapical and subsequent cone-beam computed tomography showed a radiolucent lesion at the healing site. Exploratory surgery was planned to acquire tissue for histopathologic examination and to debride the area. A full thickness flap was raised and an osteotomy was performed using a trephine bur to expose the pathologic tissue.

On removal of the cortical buccal plate, a bony lesion was detected from which a yellow–white aggregate material (similar in appearance to cottage cheese) was removed for histologic investigation (Fig. 2). The lingual cortical plate was intact. A biopsy specimen was taken from the periapical nonhealing area (4 mm below the alveolar crest) as well as adjacent normal-appearing bone. Immediately after surgery, the biopsy specimen was immersed in 10% neutral buffered formalin and dispatched to the pathology laboratory. The remaining affected area was completely debrided and irrigated with saline solution. The flap was reapproximated and sutured closed with 5-0 extended poly-tetra fluoroethylene sutures (Gortex, Gore, Flagstaff, AZ).

The patient's postoperative home care instructions included rinsing her mouth with 0.12% chlorhexidine gluconate (Peridex, 3M ESPE, West Palm Beach, FL) mouthwash and a prescription for amoxicillin (500 mg, 3 times a day for 7 days). The sutures were removed 10 days later.

Healing was uneventful and the patient reported only mild discomfort and swelling around the surgical site. Histologic examination revealed fragments of fibrous and fibrovascular connective tissue containing moderate to dense mixed and chronic inflammatory cell infiltrates (Fig. 3). Bacterial colonies exhibiting club-shaped filaments surrounded by neutrophils were observed. Also seen were speckles of vital bone, collections of foamy macrophages, fragments of foreign material consistent with root canal filling, a fragment of polarizable foreign material of unknown origin and products of hemorrhage. The pathologic diagnosis was a lesion containing bacterial colonies consistent with Actinomyces.

Based on the histologic analysis, the patient was advised to continue taking 500 mg amoxicillin for 4 more weeks. The patient was then monitored weekly during the first month and, thereafter, every month. No clinical signs or symptoms were present during the follow-up period (Fig. 4). After 4 months, a periapical radiograph revealed no extraordinary findings. Following prosthodontic evaluation, an implant was considered in the area of tooth 44. Informed consent was obtained from the patient. She was advised to take 2 g of amoxicillin 1 hour before the appointment as recommended prophylactic antibiotic treatment prior to implant surgery.13

Figure 2: Yellow–white aggregate material (similar in appearance to cottage cheese) inside the bony lesion.

Figure 3: Gram's stain showing an abundance of gram-positive, filamentous aggregates of bacteria, characteristic of Actinomyces.

Figure 4: Postoperative photograph 4 weeks after exploratory surgery showing no clinical signs or symptoms of infection.


A full-thickness flap was elevated to the extent that the apical portion of the alveolar ridge at the buccal and lingual plates was visible (Fig. 5). A narrow platform implant, 3.5-mm diameter, 10 mm long (Replace Select Tapered, Nobel Biocare, Göteborg, Sweden) was installed at the tooth 44 position (Fig. 6). Implant stability was confirmed by an insertion torque test (> 35 N cm) and a healing abutment was installed immediately after implant placement (Fig. 7). The peri-implant area was examined at 1, 2 and 4 weeks and at 3, 6, 12 and 18 months postoperatively. The patient reported no complications, and there was no infection, pain, bleeding or swelling. Peri-implant mucosa appeared a healthy, normal pink colour. At 18 months postoperatively (14 months after the implant restoration), crestal bone loss was less than 2 mm from the initial level. Probing depth was 3 mm all around. There was no implant mobility. Recession was less than 1 mm. Decreased translucency within the intrabony component of the peri-implant bone defect was apparent on radiographs (Fig. 8). The crown met the patient's expectations in terms of shape, dimensions and colour.

Figure 5: Examination of the alveolar bone revealed no visible signs of bone pathology on the buccal or lingual plate.

Figure 6: Periapical radiograph taken immediately following placement of a 3.5-mm-diameter implant in the previously infected area.


Figure 7: Clinical photograph of the surgical site 4 weeks after placing the implant with a flared healing abutment.

Figure 8: Periapical radiograph 18 months after installation of the implant. The radicular radiolucency decreased markedly over the period of treatment.



Clinical and radiographic manifestations of apical actinomycosis are usually indistinguishable from common periapical pathoses.7 Periapical actinomycosis should be included in the differential diagnosis in cases where a periapical lesion has not responded to appropriate endodontic treatment. Actinomyces has been shown to prevent normal periradicular healing following conventional endodontic therapy, even after removal of the tooth as the bacteria are able to survive in periapical tissues outside root canals.14-16 In such cases, surgical intervention along with long-term antibiotic treatment may be necessary to enable healing.

Clinical reports have suggested that a history of periodontal or endodontic infection is a predictive marker for implant infection and failure.17-20 Although several studies21-23 have supported immediate implant therapy at infected sites, this approach requires thorough debridement and achieving primary stability of the implant to allow osseointegration and subsequent implant survival. Further long-term controlled clinical trials are needed to investigate this approach.

Proper management of implant candidates with a history of local infection requires early diagnosis of the infectious disease and the administration of appropriate medications. Of paramount importance is the patient's compliance with respect to regular attendance at appointments, drug therapy and patience with the long-term management of the disease, the implant therapy and necessary follow-up.

In this article, we describe a clinical picture of chronic periapical inflammation that, on histologic examination, revealed the presence of Actinomyces colonies. Successful treatment of actinomycosis made it possible for us to offer the patient the option of implant therapy in the affected area. The patient was followed for 18 months after installation of a dental implant at the previously affected site, and we intend to follow the case for a longer period to ensure the success of the therapy.



Dr. Angaji is a periodontist in Winnipeg, Manitoba. He was senior resident in the graduate periodontics program at the University of Manitoba's faculty of dentistry when the article was written.

Dr. Brar is a periodontist in Winnipeg, Manitoba. He was senior resident in the graduate periodontics program at the University of Manitoba's faculty of dentistry when the article was written.

Acknowledgements: We thank Dr. Stephen Ahing, division head, oral diagnosis and radiology at the faculty of dentistry, University of Manitoba, for his valuable comments.

Correspondence to: Dr. Mahdi Angaji, 11 Petersfield Place, Winnipeg, MB  R3T 3V5. Email:

The authors have no declared financial interests in any company manufacturing the types of products mentioned in this article.

This article has been peer reviewed.


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