|Year : 2016 | Volume
| Issue : 2 | Page : 48-52
Management of a rare case of mandibular condylar aplasia in a resource-limited setting
Adebayo Aremu Ibikunle1, Olutayo James2, Olufemi Erinoso2, Modupe Olugbenga Ogunlewe2
1 Department of Surgery/Dental and Maxillofacial Surgery, Usmanu Danfodiyo University/Usmanu Danfodiyo University Teaching Hospital, Sokoto, Nigeria
2 Department of Oral and Maxillofacial Surgery, College of Medicine, University of Lagos, Lagos, Nigeria
|Date of Web Publication||16-Aug-2018|
Dr. Adebayo Aremu Ibikunle
Department of Oral and Maxillofacial Surgery, Usmanu Danfodiyo University Teaching Hospital, Sokoto
Source of Support: None, Conflict of Interest: None
Condylar aplasia is a rare anomaly often associated with varying functional and/or esthetic consequences. These associated challenges have been managed with different methods, including orthognathic surgery, augmentative surgery, and distraction osteogenesis (DO). Indeed, combinations of these techniques have been utilized in its management. This case report describes the management of a patient with dentofacial asymmetry secondary to condylar aplasia using DO. It also highlights the challenges of management in resource-limited settings. Acceptable functional and esthetic results were achieved.
Keywords: Condylar aplasia, dentofacial asymmetry, distraction osteogenesis
|How to cite this article:|
Ibikunle AA, James O, Erinoso O, Ogunlewe MO. Management of a rare case of mandibular condylar aplasia in a resource-limited setting. Niger J Exp Clin Biosci 2016;4:48-52
|How to cite this URL:|
Ibikunle AA, James O, Erinoso O, Ogunlewe MO. Management of a rare case of mandibular condylar aplasia in a resource-limited setting. Niger J Exp Clin Biosci [serial online] 2016 [cited 2019 Jan 16];4:48-52. Available from: http://www.njecbonline.org/text.asp?2016/4/2/48/239097
| Introduction|| |
Condylar aplasia of the mandible is a very rare anomaly, which may be genetic, developmental, or acquired in origin., Trauma and inflammatory reactions feature prominently among the acquired causes of condylar aplasia.,, Regardless of its etiology, it often results in esthetic and/or functional challenges, which stems from growth disturbance, especially when unilateral.,
Distraction osteogenesis (DO) is a biomechanical process of bone tissue formation, where the distraction forces which act between the bone segments affect the biological potential of the bone by forming a callus of determined length and height., DO was first described in the field of orthopedics by Codville who reported its use in lengthening a femur by axial distraction., However, modern DO evolved primarily from the work of Gavriel llizarov.,,
McCarthy performed the first human mandibular distraction in 1992, using an external distractor in patients with hemifacial microsomia. This signaled the beginning of successful applications of DO in the maxillofacial region. Its use in the maxillofacial region has been reported by several authors, such as in the reconstruction of segmental defects and alveolar bone augmentation. However, few have reported its use in the treatment of condylar aplasia, which itself is a rare occurrence.
Both extraoral and intraoral devices may be used. The extraoral distraction devices are not socially convenient and may leave residual skin scars, while intraoral distraction device is more convenient socially and leaves no residual skin scars.,
We present a case of a 10-year-old male with nonsyndromic, right condylar aplasia complicated by mandibular growth deficiency and resultant asymmetry. The asymmetry was successfully managed with the use of DO.
| Case Report|| |
A 10-year-old male presented with a complaint of facial asymmetry and consequent poor esthetics of 5 years' duration. There was no previous history of trauma, childhood illness, ear infection, or forceps delivery. Clinical examination revealed obvious facial asymmetry with deviation of the mandible and the chin to the right side. The left side of the face was flat and elongated, while the right side was full and appears shorter than the left [Figure 1]. The temporomandibular joint (TMJ) movement was palpable on the left only.
Intraoral examination revealed a midline shift of the occlusion to the right side by about 4 mm [Figure 2]. A three-dimensional reconstruction and computerized tomography of the face and the mandible revealed right condylar aplasia and absence of the glenoid fossa, ipsilateral prominent antegonial notch, and a mandibular deviation to the right [Figure 3] and [Figure 4]. A diagnosis of condylar aplasia was made, and DO of the right mandible was planned. An extraoral submandibular approach for placement of the DO device under general anesthesia was selected.
|Figure 2: Preoperative clinical photograph showing a midline shift to the right|
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|Figure 3: Preoperative three-dimensional reconstruction of facial skeleton|
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|Figure 4: Coronal computerized tomography showing flattened right glenoid fossa and condylar aplasia|
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Airway was maintained through the orotracheal approach. Antibiotic prophylaxis was administered (1 g of ceftriaxone) through the intravenous route. Routine scrubbing and draping were done. A 5-cm surface marking for the proposed submandibular incision was made, and 5 ml of 1:200,000 adrenaline solutions was infiltrated along the marking. Thereafter, a standard submandibular incision measuring about 5.5 cm was made and deepened using blunt dissection till the mandible and its periosteal covering were visible. A longitudinal periosteal incision was made, and the periosteum was then elevated carefully using a sharp Howarth's periosteal elevator. A marker was used to define the intended corticotomy, the longitudinal axis of the distraction device, and the screw holes as determined preoperatively.
A single continuous, circumferential osteotomy cut was made just distal to the ipsilateral first permanent molar using fissure burs and osteotome [Figure 5]. The device was then fixed to the mandible using three monocortical screws on either side of the osteotomy cut [Figure 6]. The distractor was tested intraoperatively by distracting for 2 mm and found to produce satisfactory movement of the mandibular segments. The device was then deactivated, by reapproximating the mandibular bony segments. Subsequently, suturing was done in layers with the skin closed primarily using wound adhesive (cyanoacrylate).
|Figure 6: Application of the distraction osteogenesis device intraoperatively|
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A latency period of 3 days was allowed. Distraction was done at a rate of 0.5 mm/day in two sessions for 8 days by which time the midline shift was largely corrected. The patient spent a total of 6 days on hospital admission postsurgery and had six separate activations of the DO device done, three of which were done by the parent under close supervision by the surgeon before discharge. Further activations of the device were done by the parent on outpatient basis with strict instructions to make a quarter turn in the morning and another quarter turn in the evening. To allow adequate monitoring, one of the two daily activations was done under supervision at the hospital, every other day. A consolidation phase of 6 weeks was then instituted with instructions that patient should be on soft diet. Postoperative orthopantomogram was taken to evaluate the procedure.
After the consolidation period, removal of the distractor was done through an incision placed along the preexisting surgical scar under general anesthesia. The patient was given 2-weekly appointments for the 1st month after removal of device and is now being seen monthly for review. The extraoral wound healed satisfactorily with minimal scaring. No complications were observed. There was no clinical evidence of infection during the distraction and consolidation period. The patient was evaluated using serial orthopantomogram during the postoperative period.
Satisfactory correction of facial asymmetry, mandibular occlusal midline, and improvement in mouth opening to about 3 cm was achieved [Figure 7] and [Figure 8]. The patient has been followed up for 6 months with no untoward effect of the surgery or relapse observed.
|Figure 7: Postoperative clinical photograph showing the distractor activating arm exit and the corrected midline on the 14th postoperative day|
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| Discussion|| |
Mandibular lengthening by DO was reported by McCarthy in 1994. Since then, its use in the maxillofacial region has been reported by several authors. Developmental anomalies of the mandible are varied in nature. They are often categorized into aplasia, hypoplasia, hyperplasia, and bifidity. Condylar aplasia is a rare developmental anomaly that often results in some esthetic challenges. Proposed etiological factors include trauma, radiotherapy, hormonal imbalance, and inflammatory conditions such as juvenile arthritis., Interestingly, none of these was identified in this patient; the cause of the anomaly in this case may have been due to a spontaneous genetic defect or idiopathic.,
Downward and forward growth of the affected side is impaired, resulting in significant esthetic challenges. The cheek appears full on the affected side, and the mandible deviates to the affected side. Furthermore, there may be an occlusal cant, mandibular retrognathia, as well as a shortened ramus height with resultant facial asymmetry.
The TMJ develops from the temporal and condylar blastema, which begins to develop around the 8th week of intrauterine life. The right condylar fossa was shallow in this case, which indicates that this defect may have been present prenatally. There was no history of traumatic birth delivery.
Several options for management of this condition have been proposed, including DO, use of functional appliances, surgical osteotomies, and surgical reconstruction of the joint with the use of costochondral graft. In this case report, DO was opted for because of its availability, ease of use, and existing expertise. Functional appliances such as the KLAMPT appliance have also been found quite useful for the treatment of condylar aplasia in growing patients. However, functional appliances require the cooperation of the patient; it may also require a long period of treatment and relies heavily on growth spurts.
Costochondral grafts on the other hand offer the possibility of growth and subsequent correction of the facial asymmetry; however, they may be rejected, and growth in them may be unpredictable as it grows at another rhythm compared to the condyle., Furthermore, the absence of a well-defined glenoid fossa which is required for articulation may complicate its use.
Presurgical orthodontics was done to decompensate for occlusal adaptations. A linear DO device was used. DO offers an effective alternative. It stimulates both hard- and soft-tissue growth. It was secured with monocortical screws so as to avoid developing tooth buds of the molars. Notably, a multiplanar DO device would have been preferred; however, due to financial incapacitation and limitation in resources, a uniplanar DO device was used. The multiplanar DO device offers multidirectional distraction of the bony segments, which would have been useful in this case where both horizontal and vertical deficiencies were identified.
Notwithstanding the facial asymmetry which was largely corrected by the uniplanar device used, the vertical deficiency remained uncorrected. The TMJ was also not reconstructed because of financial incapacitation. Focus was on addressing the patient's main complaint, which was the facial asymmetry. Correction of the horizontal deficiency was sufficient to address this.
Therefore, lengthening of the right body of the mandible and increment of the ramus height were planned for and achieved by placing the DO device about 4 mm from the right angle of the mandible and ensuring that the resultant force had both a vertical component and a horizontal component. Hence, the facial asymmetry, which was the primary complaint of the patient, was corrected.
| Conclusion|| |
This case report has demonstrated effective use of DO in correcting the untoward effects of condylar agenesis. We were able to correct the midline shift and improve the mouth opening of the patient.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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