Necrotizing sialometaplasia of the palate: a case report and literature review
10.12016/j.issn.2096-1456.202550529
- Author:
BU Xiangwen
1
;
YE Chuanjin
2
;
CHU Zhijuan
1
;
DUAN Ning
1
;
WANG Xiang
1
;
WANG Wenmei
1
;
PENG Qiao
1
Author Information
1. Department of Oral Mucosal Diseases, Nanjing Stomatological Hospital, Affiliated Hospital of Medical School, Institute of Stomatology, Nanjing University
2. Department of Oral Pathology, Nanjing Stomatological Hospital, Affiliated Hospital of Medical School, Institute of Stomatology, Nanjing University
- Publication Type:Journal Article
- Keywords:
oral mucosal diseases;
necrotizing sialometaplasia;
ulcer;
palate;
self-limiting;
betel nut;
his⁃topathology;
oral malignant tumors
- From:
Journal of Prevention and Treatment for Stomatological Diseases
2026;34(3):273-280
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To enhance the recognition of necrotizing sialometaplasia (NS) by elucidating its clinical, pathological characteristics and key diagnostic points, providing a basis for the diagnosis and treatment of the disease.
Methods:This study has been reviewed and approved by the Medical Ethics Committee, and informed consent has been obtained from patients. Review the data of a patient with NS occurring at the junction of the right soft and hard palate, and comprehensively analyze its diagnostic process based on its clinical manifestations, imaging, and histopathological examination results. And review the relevant literature on the disease.
Results:This study describes a 24-year-old male patient with a documented betel nut habit (2 pieces/day for >6 months), who presented with a bone-deep, irregular crateriform ulcer (3 mm × 6 mm × 5 mm) localized to the right hard-soft palate junction. Spiral CT showed a local soft tissue defect with no apparent underlying bone destruction. Histopathology demonstrated chronic inflammation of the mucosal and minor salivary gland tissues, with no evidence of malignancy. A final diagnosis of NS was established. The ulcer healed completely three weeks after initiation of local anti-inflammatory therapy. A literature review indicates that NS is a rare, benign salivary gland disorder, typically occurring at the hard-soft palate junction in middle-aged men (40-60 years). Its etiology remains unclear, but it is widely attributed to salivary lobe infarction following mechanical trauma-induced ischemia. Due to its clinical resemblance to malignancy, it is often misdiagnosed. Treatment entails local anti-inflammatory measures and meticulous wound care aimed at promoting mucosal healing.
Conclusion:NS is a self-limiting, benign condition that poses a significant diagnostic challenge due to its close clinical simulation of malignancy. Thus, accurate diagnosis requires a combined assessment of clinical presentation, radiological features, and pathological findings. Treatment is predicated based on a conservative strategy with an emphasis on symptomatic management.
- Full text:2026032015504986986腭部坏死性唾液腺化生1例及文献回顾.pdf
