Primary soft tissue Ewing’s sarcoma of the maxillary sinus in elderly patients: presentation, management and prognosis
Identifieur interne : 001808 ( Main/Merge ); précédent : 001807; suivant : 001809Primary soft tissue Ewing’s sarcoma of the maxillary sinus in elderly patients: presentation, management and prognosis
Auteurs : Mainak Dutta [Inde] ; Soumya Ghatak [Inde] ; Gautam Biswas [Inde] ; Arya Sen [Inde]Source :
- Singapore Medical Journal [ 0037-5675 ] ; 2014.
Abstract
Nonosseous or soft tissue Ewing’s sarcoma is a rare form of Ewing’s sarcoma/primitive neuroectodermal tumour that seldom affects the head and neck region. Involvement of the nose and paranasal sinuses is extremely uncommon, with only eight of such patients being reported to date, mostly affecting adolescents and young adults. To our knowledge, this study is the first comprehensive report of primary soft tissue Ewing’s sarcoma involving the paranasal sinuses in an elderly patient who successfully completed treatment. We herein discuss the pathogenesis, management and factors affecting the prognosis of this rare group of tumours involving the nose and paranasal sinuses, in relation to the available literature.
Url:
DOI: 10.11622/smedj.2013263
PubMed: 24442190
PubMed Central: 4294066
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PMC:4294066Le document en format XML
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<front><div type="abstract" xml:lang="en"><p>Nonosseous or soft tissue Ewing’s sarcoma is a rare form of Ewing’s sarcoma/primitive neuroectodermal tumour that seldom affects the head and neck region. Involvement of the nose and paranasal sinuses is extremely uncommon, with only eight of such patients being reported to date, mostly affecting adolescents and young adults. To our knowledge, this study is the first comprehensive report of primary soft tissue Ewing’s sarcoma involving the paranasal sinuses in an elderly patient who successfully completed treatment. We herein discuss the pathogenesis, management and factors affecting the prognosis of this rare group of tumours involving the nose and paranasal sinuses, in relation to the available literature.</p>
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