Intraductal papilloma is a rare benign epithelial neoplasm of the salivary duct system, characterized by papillary proliferation of ductal epithelium into a cystic lumen. It predominantly occurs in minor salivary glands, particularly in the lips and buccal mucosa, and is rarely found in the mandibular region. We report a case of intraductal papilloma in the left retromolar trigone of a 46-year-old woman. Clinically, the lesion presented as a painless, well-circumscribed bluish submucosal mass. Radiographic findings were nonspecific, and a provisional diagnosis of hemangioma was made. The lesion was surgically excised under general anesthesia. Histopathological examination revealed a cystic cavity lined by cuboidal to columnar epithelial cells with intraluminal papillary projections, consistent with intraductal papilloma. Scattered mucous-producing cells were also noted. No evidence of recurrence was noted at the 24-month follow-up. This case highlights the importance of histopathological confirmation in diagnosing intraoral submucosal lesions.
A 48-year-old woman visited the oral and maxillofacial surgery department complaining of swelling under the left mandible. The patient said that the size of the small lump had not changed much since it was first discovered, but it seemed to have grown slightly recently after 5 years. She visited another hospital 1 week ago and had a CT scan, but no specific findings were found. A firm and mobile mass was palpated in the submandibular gland area during clinical examination. Ultrasound imaging and contrast-enhanced CT were performed, and the patient was diagnosed with pleomorphic adenoma. Submandibular gland resection was performed, and the mass was confirmed as pleomorphic adenoma by histopathological examination. There has been no recurrence to date, 8 years later. In this study, we will examine the diagnostic process of a rare submandibular gland pleomorphic adenoma and review the literature.
Localized juvenile spongiotic gingival hyperplasia (LJSGH) is a rare gingival lesion predominantly affecting individuals aged <20 years. Although it has a distinct clinical presentation, its underlying pathogenesis remains poorly understood and standardized treatment guidelines are yet to be established. Surgical excision is the most common treatment; however, concerns regarding recurrence, aesthetic impact, and patient cooperation, particularly in pediatric cases, highlight the need for alternative approaches. Although spontaneous regression of LJSGH has been suggested, well-documented cases are rare. This report presents a case of LJSGH demonstrating spontaneous resolution without surgical intervention. A lesion on the mandibular anterior facial gingiva fully resolved over a 32-month period, further supporting the potential for natural resolution, and emphasizing the need for a conservative management approach.