| Literature DB >> 26191120 |
Dong-Ni Zhou1, Qing-Qing Yang2, Zhong-Lin Li3, Zhi-Yong Pan4, Yan-Fei Deng5.
Abstract
Head and neck rhabdomyosarcoma (HNRMS) is exceedingly rare and poorly documented. The difficult diagnosis often causes a poor prognosis and high mortality. Hence, we report 4 cases of HNRMS and their follow-up outcomes, and review the clinicopathological features of this rare tumor. The 4 patients ranged in age from 5 to 29 years. Among them, 3 patients had a good prognosis after combination of radiotherapy and chemotherapy or surgery alone. Another patient survived for only 3 months after diagnosis without therapy. Deeply insight into HNRMS might improve the ability of diagnosis and treatment for this disease.Entities:
Keywords: Rhabdomyosarcoma; follow-up; head and neck
Mesh:
Year: 2015 PMID: 26191120 PMCID: PMC4502992
Source DB: PubMed Journal: Int J Clin Exp Pathol ISSN: 1936-2625