Department of Otorhinolaryngology and Head & Neck Surgery, Hospital de Braga, Braga, Portugal
Department of Otorhinolaryngology and Head & Neck Surgery, Hospital de Braga, Braga, Portugal.
BMJ Case Rep. 2020 May 20;13(5):e232460. doi: 10.1136/bcr-2019-232460.
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.
小儿鼻-鼻窦肿瘤有多种病因。尤因氏肉瘤(Ewing's sarcoma,ES)是一种神经外胚层来源的恶性肿瘤。这种肉瘤主要影响儿童和青少年,可以是骨内或骨外形式。头颈部原发性 ES 极为罕见,仅占所有病例的 4%-9%。据我们所知,目前文献中仅报道了少数几例鼻 ES 病例。作者报告了一例先前健康的 12 岁女孩,她表现为快速生长和扩张的额部肿块和单侧鼻塞。病变的免疫组织化学、分子和细胞遗传学分析显示肿瘤细胞弥漫表达 CD56 和 CD99,以及涉及染色体 22q12 的易位,证实了 ES 的诊断。