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Lymphatic malformation of the masseter: A case report
Sanjay Kumar1, Padmanidhi Agarwal1, Divya Mehrotra1
1Department of Oral and Maxillofacial Surgery, King George's Medical University, Lucknow, India.
This case report details a rare lymphatic malformation in the masseter muscle, a condition seldom seen in this location. Diagnosis involved fine needle aspiration and CT scans, with surgical excision confirming the findings.
Area of Science:
- Head and Neck Surgery
- Vascular Surgery
- Dermatology
Background:
- Intramuscular vascular malformations are rare, affecting less than 1% of skeletal muscles.
- Lymphatic malformations are less common vascular malformations, with rare occurrences in the masseter muscle.
- Head and neck region accounts for 15% of intramuscular vascular malformations.
Purpose of the Study:
- To report a rare case of lymphatic malformation in the masseter muscle.
- To highlight the diagnostic and management approach for this rare condition.
- To emphasize the rarity of masseter lymphatic malformations and their late presentation.
Main Methods:
- Case presentation of a 27-year-old male with a cheek swelling.
- Diagnostic workup included fine needle aspiration (FNA) and Computed Tomography (CT) scans.
- Surgical excision of the masseter lesion followed by histopathological confirmation.
Main Results:
- Histopathological examination confirmed a lymphatic malformation of the masseter muscle.
- The patient presented with a one-year history of cheek swelling.
- This represents a rare instance of masseter lymphatic malformation with a late onset.
Conclusions:
- Lymphatic malformation of the masseter muscle is exceptionally rare, particularly with late presentation.
- Accurate diagnosis relies on imaging (CT) and FNA, with surgical excision as the definitive treatment.
- Long-term follow-up is essential to monitor for potential recurrence of the malformation.
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