Related Experiment Video
Updated: Jul 5, 2026

Endoscopic Third Ventriculostomy and Pineal Biopsy from a Single Entry Point
Published on: June 28, 2024
[Parotid gland's tumors in children]
Fernández Córdoba1, J Gonzálvez Piñera, J P García De La Torre
1Sección de Cirugía Pediátrica, Complejo Hospitalario Universitario de Albacete.
Insights
Pediatric salivary gland tumors, particularly in the parotid gland, are rare but have a higher malignancy risk in children. Early diagnosis and surgical excision are crucial for effective treatment.
Area of Science:
- Pediatric Oncology
- Head and Neck Surgery
- Pathology
Context:
- Salivary gland tumors are uncommon in children, with parotid gland involvement in 80% of cases.
- Malignancy risk is elevated in pediatric salivary gland tumors compared to adults.
Purpose:
- To review eight pediatric cases of salivary gland tumors treated at a single hospital.
- To analyze the clinical presentation, histological features, diagnostic methods, and treatment outcomes.
Summary:
- Eight patients aged 14 years and younger presented with slow-growing, painless parotid masses.
- Diagnoses included pleomorphic adenomas, hemangiomas, epidermal cysts, and one rare myoepithelial carcinoma.
- Fine needle aspiration biopsy had variable diagnostic accuracy; surgical resection was the primary treatment, with total parotidectomy for malignant and recurrent cases.
Impact:
- Highlights the diagnostic challenge as malignant and benign parotid tumors are clinically indistinguishable in children.
- Emphasizes the need for prompt diagnosis and wide surgical margins for pediatric salivary gland tumors.
- Suggests adjuvant therapies may be less effective in pediatric patients compared to adults.
Abstract:
The tumors of the salivary glands are infrequent in children, and parotid gland is involved in 80% of them. When a salivary gland tumor is present, the chance of malignancy is greater in the child than in the adult. We reviewed 8 cases identified in patients aged 14 years and younger in our hospital, analyzing its antecedents, signs and symptoms, histological features, diagnosis, treatment and evolution. All the patients displayed preauricular painless, non-inflammatory and slow-growing masses to an age between 10 months and 14 years. Four or them were pleomorphic adenomas, two haemangiomas, one epidermal cysts and one myoepithelial carcinoma. We emphasize the exceptional nature of the carcinoma for its rareness and for the high degree of malignancy expressed. We made a fine needle aspiration biopsy in four cases but they were conclusive only in three. All were treated by surgical resection of the tumour except for the myoepithelial carcinoma and the recurrent pleomorphic adenoma that were treated by total parotidectomy. The malignant tumours of the parotid gland are clinically indistinguishable of the benign ones, thus when any palpable mass appears in the zone of the parotid gland, an accurate diagnosis should be made without delay. The treatment of choice is the surgical excision with wide margins, being other adjuvant treatments less useful to this age than in the adult age.
Related Concept Videos
The Retinoblastoma Gene
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
The Retinoblastoma Gene
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
The Parathyroid Glands
Oxyphil cells, whose functions remain elusive, emerge during late puberty, adding a layer of complexity to the parathyroid gland's intricacies. In contrast, principal parathyroid cells undertake a vital role by producing...
