Objectives
This prospective clinical trial aimed to examine the predictability of maxillary canine transplantation as compared to biological canine eruption. Additional objectives were to examine hard and soft tissue outcomes, including aesthetic outcome compared to outcomes with the contralateral canines.
Settings and Sample Population
The sample comprised 17 consecutively transplanted maxillary canines in 17 patients (mean age at surgery, 18 years; range, 11‐29 years). Minimal follow‐up time was 12 months post‐transplantation. Clinical and radiographic parameters were recorded for the transplanted and contralateral canines, showing a natural eruption pattern.
Material and Methods
The Maxillary Canine Aesthetic Index (MCAI) and the Autotransplanted Maxillary Canine Radiological Index (AMCRI) were scored for all upper canines. Successful transplantation was considered as the absence of pathology during intermittent clinical and radiographic controls and a good‐to‐excellent outcome compared to the contralateral biological erupted canine, as defined by the MCAI and AMCRI.
Results
The mean follow‐up period was 28 months (±9; range, 12‐40 months). The overall survival rate was 100%, and the success rate reached 68% at 1 year post‐operatively. Significant predictors of success were the extra‐oral time during transplantation, amount of damage to the root surface, quality of surrounding tissues and immediate post‐operative oral hygiene.
Conclusion
Standardized measurements demonstrated clinically satisfactory outcomes with maxillary canine autotransplantation compared to outcomes with the contralateral canine during 1‐3 years of follow‐up. The potential predictors of success identified here should be confirmed with long‐term follow‐up studies.
Trigeminal sensory neuropathy can be caused by a variety of conditions, including local, traumatic, iatrogenic, or systemic causes. Diagnosis and management remain a challenge for maxillofacial surgeons and neurologists. Therefore, a good clinical examination and objective tests and imaging are needed when diagnosing patients who present with facial numbness. We present a case with spontaneous episodes of facial paresthesia. He was diagnosed with hereditary neuropathy with liability to pressure palsies (HNPP), a rare condition that affects the peripheral nerves. Only a few case reports that describe involvement of the cranial nerves in patients with HNPP were found in the literature, and facial paresthesia has not been previously reported.
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