ISSN: 2161-0681

Journal of Clinical & Experimental Pathology
Open Access

Our Group organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)

Case Report

Oral Rhabdomyosarcoma: A Case Report

Deyhimi Parviz* and Khalesi Saeideh

Department of Oral & Maxillofacial Pathology, Dentistry School, Isfahan University of Medical Sciences, Isfahan, Iran

*Corresponding Author:
Parviz Deyhimi
Associate Professor
Department of Oral & Maxillofacial Pathology
Dentistry School, Isfahan University of Medical Sciences, Isfahan, Iran
Tel: 0098-311-7922879
E-mail: Deihimy@dnt.mui.ac.ir

Received Date: December 10, 2013; Accepted Date: February 19, 2014; Published Date: February 21, 2014

Citation: Parviz D, Saeideh K (2014) Oral Rhabdomyosarcoma: A Case Report. J Clin Exp Pathol 4:161. doi: 10.4172/2161-0681.1000161

Copyright: © 2014 Parviz D, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Rhabdomyosarcoma (RMS) is a malignant soft tissue neoplasm of skeletal muscle origin. The most common sites of occurrence are the head and neck, genitourinary tract, and extremities. Although Rhabdomyosarcoma has a relative predominance for head and neck region, it is less frequent in oral cavity, and accounts for only 0.04% of all head and neck malignancies. Some studies have been showed that soft palate and tongue are the most common sites for oral RMS. We present a case of oral Rhabdomyosarcoma in a 15 year old girl, and demonstrate the clinical, radiological, histological, and immunohistochemical features of this neoplasm.

Keywords

Top