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Intermuscular Fibrolipoma of the Neck: A Rare Case Report
Kamal Nain Rattan1,2, Vijay Kalra3, Anshu Mangla3
1Present Address: SPES Hospital, Sheila bypass road, Rohtak, Haryana India.
Summary
This case report details a rare pediatric neck mass: an intermuscular fibrolipoma. Surgical resection was successful, highlighting the importance of considering rare diagnoses in pediatric neck tumors.
Area of Science:
- Pediatric Surgery
- Oncology
- Pathology
Background:
- Lipomas are benign tumors, typically slow-growing and uncommon in children.
- Intermuscular fibrolipomas are a rare subtype, characterized by their location within muscle tissue.
Purpose of the Study:
- To report an extremely rare case of an intermuscular fibrolipoma in a pediatric patient.
- To emphasize the diagnostic considerations and successful management of such rare neck masses in children.
Main Methods:
- A 3-year-old child presented with a right-sided neck mass and limited neck mobility.
- Diagnostic imaging included ultrasound and computed tomography (CT) of the neck.
- Complete surgical resection of the mass was performed.
Main Results:
- Imaging suggested an intermuscular lipoma.
- Histopathological examination confirmed the diagnosis of intermuscular fibrolipoma.
- The patient experienced a successful outcome following surgical intervention.
Conclusions:
- Intermuscular fibrolipomas are exceptionally rare in the pediatric population, particularly in the posterior neck.
- Complete surgical excision is an effective treatment modality.
- This case underscores the need for thorough evaluation of pediatric neck masses, even those with unusual presentations.

