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An unusual tongue base mass in an infant: Tongue base sialolipoma
Dawn T Teo1, Romaine F Johnson, John E McClay
1Department of Pediatric Otolaryngology, Children's Medical Center Dallas, UT Southwestern Medical Center at Dallas, 5323 Harry Hines Blvd., Dallas, TX 75390, USA. dawnttw@gmail.com.
Insights
This study reports the first pediatric case of sialolipoma, a rare tumor, found at the tongue base. Successful surgical removal in an infant led to no recurrence at one year.
Area of Science:
- Otorhinolaryngology
- Pediatric Pathology
Background:
- Sialolipoma is a rare benign tumor originating from salivary glands, typically affecting the head and neck region.
- While common in adults, pediatric cases are exceptionally rare, with limited documentation in medical literature.
Observation:
- A 6-month-old infant presented with progressive dysphagia, reflux, and snoring.
- Physical examination revealed a significant mass at the base of the tongue.
- Surgical exploration and subsequent histological analysis confirmed the mass as a sialolipoma.
Findings:
- Histological examination identified a well-circumscribed lesion comprising mature adipose tissue with entrapped salivary gland elements.
- The findings were consistent with a sialolipoma, a rare salivary gland tumor.
- This represents the first documented instance of a sialolipoma occurring at the tongue base in a pediatric patient.
Implications:
- This case highlights the importance of considering sialolipoma in the differential diagnosis of pediatric neck masses presenting with airway or feeding difficulties.
- Early diagnosis and surgical management appear effective, with no recurrence observed at one-year follow-up.
- Further research into pediatric sialolipomas may improve understanding and management of these rare tumors.
Abstract:
Sialolipoma is a rare tumor that occurs in the head and neck. We present a case arising from a minor salivary gland in an infant. The 6-month-old infant presented with difficulty swallowing, frequent reflux, and snoring that had been worsening several weeks before presentation. Physical examination showed a large mass arising from the tongue base. The patient was taken to the operating room for transoral removal of a presumed cyst. Histologic examination of the lesion showed a well-circumscribed lesion composed of lobules of mature adipose tissue and nodules of entrapped, non-neoplastic acini and ductules separated by thin, fibrous septae, consistent with a sialolipoma. To the best of our knowledge, this is the first reported case of a sialolipoma at the tongue base in a child. The patient has had no evidence of recurrence at 1 year of follow-up.
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