Related Experiment Video
Updated: Jul 15, 2026
11:31
Repair of a Critical-sized Calvarial Defect Model Using Adipose-derived Stromal Cells Harvested from Lipoaspirate
Published on: October 31, 2012
15.8K
Giant Lipoma Involving the Face in a Child: A Rare Case Report
T N Janakiram1, Soumya Sampath1, Mansi A R Venkatramanan1
1Royal Pearl Hospital, Tiruchirapalli, Tamilnadu India.
Summary
Recurrent pediatric head and neck lipomas are rare. This case highlights the successful surgical excision of a large, recurring facial lipoma in a 15-month-old child using a facelift approach.
Area of Science:
- Pediatric Surgery
- Dermatologic Oncology
- Head and Neck Surgery
Background:
- Lipomas, benign adipose tissue tumors, are uncommon in children, especially in the head and neck.
- Recurrence of pediatric head and neck lipomas can occur, posing surgical challenges.
Purpose of the Study:
- To describe a rare case of a recurrent pediatric facial lipoma.
- To detail the diagnostic workup and surgical management of this challenging condition.
- To emphasize the utility of a facelift approach for optimal cosmetic and functional outcomes in pediatric facial tumor excision.
Main Methods:
- Case report of a 15-month-old male with a recurrent facial swelling.
- Diagnostic imaging including Magnetic Resonance Imaging (MRI) and Fine Needle Aspiration Cytology (FNAC).
- Surgical excision utilizing a facelift approach for scar concealment and facial nerve protection.
Main Results:
- Histopathological confirmation of lipoma.
- Successful complete tumor extirpation with no immediate complications.
- The facelift approach facilitated scar camouflage and preserved facial nerve function.
Conclusions:
- Recurrent facial lipomas in infants require careful diagnostic evaluation and surgical planning.
- A facelift approach can be a safe and effective technique for managing pediatric facial lipomas, ensuring excellent cosmetic results.
More Related Videos
Related Concept Videos
01:20The Retinoblastoma Gene
Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
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 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,...
01:20The Retinoblastoma Gene
Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
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 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,...