Oral Rhabdomyosarcoma: a review
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Oral Rhabdomyosarcoma: a review

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Oral Rhabdomyosarcoma: a review

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dc.contributor.author Tandon, Ankita es
dc.contributor.author Sethi, Kanika es
dc.contributor.author Singh, Anand Pratap es
dc.date.accessioned 2014-05-21T12:45:29Z
dc.date.available 2014-05-21T12:45:29Z
dc.date.issued 2012 es
dc.identifier.uri http://hdl.handle.net/10550/35284
dc.source Tandon, Ankita ; Sethi, Kanika ; Singh, Anand Pratap. Oral Rhabdomyosarcoma: a review. En: Journal of Clinical and Experimental Dentistry, 2012, Vol. 4, No. 5: 302-308 es
dc.subject Odontología es
dc.subject Ciencias de la salud es
dc.title Oral Rhabdomyosarcoma: a review es
dc.type info:eu-repo/semantics/article en
dc.type info:eu-repo/semantics/publishedVersion en
dc.subject.unesco UNESCO::CIENCIAS MÉDICAS es
dc.description.abstractenglish Rhabdomyosarcoma (RMS) is a rare malignant soft tissue neoplasm comprised of cells derived from the primitive mesen¬chyme. About 35% of RMS arises in the head and neck, are are classified as parameningeal and non-parameningeal forms. These are the most common soft tissue sarcoma of the children, adolescents and young adults. Their etiopathogenesis and its molecular relevance have been emphasized. The first line of treatment is radical excision and this is usually supplemented by radiotherapy. It is believed that adjunct combination chemotherapy may greatly improve the prognosis. Inadequately treated tumours grow in an infiltrative manner and recur in a high percentage of cases. Bone does not constitute an effective barrier to the growth of the tumour and bone invasion is a frequent finding in head and neck rhabdomyosarcomas. es

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