Affiliation:
1. St. Stephen’s Hospital, Tis Hazari, Delhi, India
2. S
Abstract
Rhabdomyosarcoma is a malignant neoplasm of mesenchymal cells, which shows varying degrees of striated muscle cell differentiation. It predominantly occurs in children while rarely found in adults. Involvement of the oral cavity accounts for only 10-12% of all head and neck cases. Herewith, we report a rare case of oral spindle cell / sclerosing rhabdomyosarcoma in a 47-year-old male presented with a small mass involving the gingiva of right upper incisor. The mass was excised with a preoperative diagnosis of gingival epulis and subjected to histopathological and immunohistochemical examination which confirmed it to be spindle cell / sclerosing rhabdomyosarcoma. Data regarding its clinical course, genetic abnormalities and prognosis as a combined subtype is scant.
Publisher
IP Innovative Publication Pvt Ltd
Reference18 articles.
1. Weiss SW, Goldblum JR, .Enzinger and Weiss's Soft Tissue Tumors 2020;7:652-652
2. Fletcher, C. D. M., .WHO Classification of Tumours of Soft Tissue and Bone.134-139
3. Cavazzana A O, Schmidt D, Ninfo V, Harms D, Tollot M, Carli M, Spindle cell rhabdomyosarcoma. A prognostically favorable variant of rhabdomyosarcoma.Am J SurgPathol 1992;16:229-264
4. Mentzel T, Katenkamp D, Sclerosing, pseudovascularrhabdomyosarcoma in adults. Clinicopathological and immunohistochemical analysis of three cases.Virchows Arch 2000;436:305-316
5. Mentzel T, Kuhnen C, Spindle cell rhabdomyosarcoma in adults: clinicopathological and immunohistochemical analysis of seven new cases.Virchows Arch 2006;449:554-60