| Literature DB >> 32439742 |
Isabel Esteves Costa1, Ana Sousa Menezes2, Antonio Fontes Lima2, Berta Rodrigues2.
Abstract
Paediatric sinonasal tumours comprise numerous aetiologies. Ewing's sarcoma (ES) consists of a malignancy of neuroectodermal origin. This type of sarcoma affects mainly children and adolescents and can assume the skeletal or extra-skeletal form. Primary ES of head and neck is extremely rare, accounting for only 4%-9% of all cases. So far, as much as we know, only a few cases of sinonasal ES have been reported in literature. The authors present a case of a previous healthy 12-year-old girl who presented with a rapidly growing and expansive frontal mass and unilateral nasal obstruction. Immunohistochemical, molecular and cytogenetic analysis of the lesion showed diffuse expression of CD56 and CD99 on tumour cells and a translocation involving chromosome 22q12, confirming ES diagnosis. © BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: chemotherapy; ear, nose and throat/otolaryngology; head and neck cancer; paediatric oncology; paediatrics (drugs and medicines)
Mesh:
Year: 2020 PMID: 32439742 PMCID: PMC7247392 DOI: 10.1136/bcr-2019-232460
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X