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.
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Costa, I. E., Sousa Menezes, A., Lima, A. F., & Rodrigues, B. (2020). Extra-skeletal Ewing’s sarcoma of the frontal sinus: A rare disorder in pediatric age. BMJ Case Reports, 13(5). https://doi.org/10.1136/bcr-2019-232460
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