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额窦骨外尤文肉瘤:儿科罕见疾病。

Extra-skeletal Ewing's sarcoma of the frontal sinus: a rare disorder in pediatric age.

机构信息

Department of Otorhinolaryngology and Head & Neck Surgery, Hospital de Braga, Braga, Portugal

Department of Otorhinolaryngology and Head & Neck Surgery, Hospital de Braga, Braga, Portugal.

出版信息

BMJ Case Rep. 2020 May 20;13(5):e232460. doi: 10.1136/bcr-2019-232460.

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.

摘要

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。

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本文引用的文献

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Rare case of extraskeletal Ewings sarcoma of the sinonasal tract.鼻窦外尤文肉瘤罕见病例。
J Cancer Res Ther. 2012 Jan-Mar;8(1):142-4. doi: 10.4103/0973-1482.95197.
6
Ewing's family of tumors of the sinonasal tract and maxillary bone.鼻窦和上颌骨的尤因氏肿瘤家族
Head Neck Pathol. 2011 Mar;5(1):8-16. doi: 10.1007/s12105-010-0227-x. Epub 2010 Nov 25.

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