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Ultrasonographic Evaluation of Salivary Glands for Sjogren's Syndrome: Diagnostic and Monitoring Insights
Published on: October 13, 2023
[Salivary gland tumors in children]
Juliette Thariat1, Pierre-Olivier Vedrine, Daniel Orbach
1University Nice Sophia-Antipolis, Anti Cancer Centre Antoine-Lacassagne, Department of Radiation Oncology/IBDC CNRS UMR 6543, 33, avenue Valombrose, 06189 Nice Cedex 2, France. jthariat@hotmail.com
Insights
Pediatric salivary gland tumors are rare but frequently malignant, unlike adult tumors. Early diagnosis and surgical treatment are crucial for epithelial tumors, with radiotherapy and chemotherapy used selectively.
Area of Science:
- Pediatric oncology
- Head and neck surgery
- Tumor pathology
Context:
- Salivary gland tumors represent 8-10% of pediatric head and neck tumors.
- Clinicians must consider these rare tumors in children presenting with non-inflammatory masses.
- Pediatric salivary gland tumors have a higher malignancy rate (50%) compared to adults (10-25%).
Purpose:
- To highlight the unique characteristics of pediatric salivary gland tumors.
- To emphasize the importance of prompt diagnosis and appropriate management strategies.
- To inform clinicians about the differential diagnosis and treatment options for these rare pediatric neoplasms.
Summary:
- Epithelial tumors are the most common type in children, with mucoepidermoid carcinomas of the parotid gland being particularly prevalent.
- Surgery is the primary treatment modality for epithelial salivary gland tumors.
- Adjuvant radiotherapy is considered for unfavorable prognostic factors, balancing benefits against risks of growth defects and secondary cancers. Chemotherapy has a limited role, reserved for unresectable or metastatic cases.
Impact:
- Increased awareness among clinicians can lead to earlier diagnosis and improved patient outcomes.
- Understanding the higher malignancy risk in children underscores the need for specialized pediatric care.
- This information aids in tailoring treatment strategies, optimizing surgical intervention, and judiciously applying adjuvant therapies to minimize long-term sequelae.
Abstract:
Salivary gland tumors in children are rare: they correspond to 8-10% of head and neck pediatric tumors. Clinicians of all disciplines should be aware of this diagnosis in front of non-inflammatory mass of the parotid or in the territory of other salivary glands. In children, 50% of salivary gland tumors are malignant which contrasts with a 10-25% risk in adults. Epithelial tumors are the most common, mucoepidermoïd carcinomas of the parotid in particular. Surgery is the treatment of choice in epithelial tumors. Adjuvant radiotherapy may be indicated in case of unfavorable prognostic factors but must be balanced with the risk of radiation-induced growth defects and secondary cancer. The role of chemotherapy is limited in these tumors, but should be discussed in case of an inoperable or metastatic lesion.
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