| Literature DB >> 26628304 |
Shipra Agarwal1, Gaurav P S Gahlot1, Ashu Bhalla2, Sameer Bakhshi3.
Abstract
Small cell osteosarcoma is a rare tumour that histologically mimics Ewing sarcoma, mesenchymal chondrosarcoma and lymphoma, the presence of osteoid being diagnostic. This variant needs different management protocol, being non-radiosensitive and behaving more aggressively than conventional osteosarcoma. The aim of this article is to highlight such an entity at an unusual site--the parietal region--with unique diagnostic, treatment and prognostic considerations in a 16-year-old girl. 2015 BMJ Publishing Group Ltd.Entities:
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Year: 2015 PMID: 26628304 PMCID: PMC4680564 DOI: 10.1136/bcr-2015-210086
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X