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一例鼻窦原发性尤因肉瘤。

A sinonasal primary Ewing's sarcoma.

作者信息

Howarth K L, Khodaei I, Karkanevatos A, Clarke R W

机构信息

Department of Otolaryngology, Royal Liverpool Childrens' Hospital, Eaton Road, West Derby, Liverpool, L12 2AP, UK.

出版信息

Int J Pediatr Otorhinolaryngol. 2004 Feb;68(2):221-4. doi: 10.1016/j.ijporl.2003.09.011.

Abstract

Nasal fractures are a common complaint familiar to all otolaryngologists. Sinonasal primary Ewing's sarcomas are extremely rare. The case of a 9-year-old boy is presented whose nasal fracture and subsequent lateral nasal wall hematoma revealed an underlying Ewing's sarcoma. There are several unusual features in the history and clinical course of this patient. Following biopsies, immunohistochemistry proved essential in distinguishing a Ewing's sarcoma from other small cell tumours. It is important that a seemingly common condition can be the first presentation of a less common, more sinister pathology.

摘要

鼻骨骨折是所有耳鼻喉科医生都熟悉的常见病症。鼻窦原发性尤因肉瘤极为罕见。本文报告了一名9岁男孩的病例,其鼻骨骨折及随后出现的鼻侧壁血肿揭示了潜在的尤因肉瘤。该患者的病史和临床过程有几个不寻常的特征。活检后,免疫组化对于鉴别尤因肉瘤与其他小细胞肿瘤至关重要。看似常见的病症可能是较罕见、更凶险病理情况的首发表现,认识到这一点很重要。

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