Odontoblastoma is a rare tumor in the oral cavity that usually develops from the epithelial cells of the developing tooth germ and occurs primarily in the mandible. Although these tumors are usually benign, they can cause serious facial deformities and other health problems if left untreated. This article will analyze the characteristics, types, diagnosis, and treatment of odontoblastoma and explore its impact on quality of life.
Odontogermoma is often found in adolescents or young adults and is usually associated with unerupted teeth.
According to the 2017 classification of the World Health Organization (WHO), odontoblastoma is mainly divided into four types:
Odontoblastomas can occur in both the upper and lower jaws, however 80% are located in the lower jaw, especially in the hind limbs. These tumors are often associated with unerupted teeth and may cause displacement and root resorption of surrounding teeth. Patients experience chronic, painless swelling and often develop facial deformities.
If the tumor is not treated, it may spread to the nasal cavity and oral cavity, causing breathing difficulties and even causing a crisis.
Initial diagnosis of odontoblastoma relies on radiographic examination, but definitive diagnosis requires a biopsy. On radiographic images, the tumor area usually appears as a round, well-defined bony shadow, with cystic features that may be seen as a "soap bubble" appearance. Common differential diagnoses include keratocyst, central giant cell granuloma, and odontogenic myxoma.
The most common treatment for odontoblastoma is surgical resection. Although chemotherapy and radiotherapy have not been proven to be effective in some cases, surgery remains the treatment of choice. Studies have shown that if the tumor is completely removed while retaining a certain amount of surrounding normal tissue, the prognosis will be more ideal.
During surgery, doctors must remove the entire tumor and at least 10 mm of surrounding normal bone tissue to reduce the chance of recurrence. Larger odontoblastomas may require removal of part of the jawbone and bone grafting. According to a systematic review, 79% of tumors require resection, while conservative treatment requires careful selection of appropriate cases.
Regular follow-up examinations are essential for patients with odontoblastoma. About 50% of patients will experience recurrence within 5 years after surgery, so annual examinations are required, especially for patients with obvious symptoms. In some cases, recurrence can occur many years after surgery.
Effective follow-up and further treatment require flexible adjustment according to individual case circumstances.
The latest research reveals that BRAF V600E gene mutations occur at a relatively high frequency in odontoblastoma, and these mutations lead to excessive activation of cell proliferation signals. These results provide new ideas for future treatments.
Although odontoblastoma is a benign tumor, the facial deformity and impact on quality of life it causes cannot be underestimated. Based on the current clinical data and research results, how to more effectively prevent and treat this type of tumor has become a new challenge for clinicians and experts. So, what new treatment options will be developed in the future to address this worrying health problem?