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Journal of Advances in Medicine and Medical Research, ISSN: 2456-8899, ISSN: 2231-0614 (Past),Vol.: 23, Issue.: 10

Case Report

Oral Fibrolipoma-: A Rare Presentation Case Report and Review of Literature

 

Rohit Mishra1, Neha Bhasin2*, Anurag Sahu3 and Sonalika Ghate4

1Department of Periodontics, Hitkarini Dental College and Hospital, Madhya Pradesh Medical Science University, India.

2Department of Oral Medicine and Radiology, Hitkarini Dental College and Hospital, Madhya Pradesh Medical Science University, India.

3Department of Orthodontics, Hitkarini Dental College and Hospital, Madhya Pradesh Medical Science University, India.

4Department of Oral Pathology and Microbiology, Hitkarini Dental College and Hospital, Madhya Pradesh Medical Science University, India.

Article Information

Editor(s):

(1) James Anthony Giglio, Adjunct Clinical Professor of Oral and Maxillofacial Surgery, School of Dentistry, Virginia Commonwealth University, Virginia, USA.

Reviewers:

(1) Takahiro Kanno, Shimane University Faculty of Medicine, Japan.

(2) Manas Bajpai, NIMS Dental College, Jaipur, India.

(3) Ihsan Yıldız, Suleyman Demirel University, Turkey.

Complete Peer review History: http://www.sciencedomain.org/review-history/20841

Abstracts

Lipomas are classified as benign soft tissue neoplasms of mesenchymal origin and comprise 4-5% of benign tumors in the body. They are relatively rare in the oral cavity with a rate of 1/5000 individuals. The buccal mucosa, tongue, and floor of the mouth are among the common locations. Surgical excision is the treatment of choice. The fibrolipoma is an unusual histologic variant of lipoma that is comprised of neoplastic fat cells embedded in condensed collegen tissue.  Clinicians should be aware of these lesions in order to develop better clinical differential diagnoses. This is a report of a rare case of an oral fibrolipoma in an unusual location in the lower labial oral mucosa.  The biological characteristics of the lesion are described.

Keywords :

Labial mucosa; oral fibrolipoma; rare.

Full Article - PDF    Page 1-5

DOI : 10.9734/JAMMR/2017/35854

Review History    Comments

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