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Intramuscular haemangioma of mylohyoid muscle: A case report.

作者信息

Nair Arun B, Manjula B V, Balasubramanyam A M

机构信息

Department of Otolaryngology and Head and Neck Surgery, St. Johns Medical College and Hospital, Bangalore, India.

出版信息

Indian J Surg. 2010 Jul;72(Suppl 1):344-6. doi: 10.1007/s12262-010-0079-3. Epub 2010 Oct 20.

Abstract

OBJECTIVE

To report a case of intramuscular haemangioma (IMH) with a rare presentation in the mylohyoid, with emphasis on the clinical appearance, and histologic characteristics of the lesion.

METHOD

Case report and review of the literature.

CONCLUSION

Neck swellings can often present a diagnostic dilemma, with a wide preoperative differential diagnosis. IMH are rare benign haemangiomas occurring within the skeletal muscle. They account for approximately 1% of all haemangiomas. These are uncommon in the head and neck region and occur most frequently in the trunk and extremities. In the head and neck, masseter and trapezius are the most common sites involved. Intramuscular haemangioma is seldom diagnosed preoperatively, perhaps due to unfamiliarity with this uncommon lesion and nonspecific clinical findings.

摘要

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Intramuscular haemangioma of mylohyoid muscle: A case report.
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