组织病理学
医学
血管纤维瘤
耳鼻咽喉科
青少年鼻咽血管纤维瘤
少年
人口
组织学
鼻中隔
病理
皮肤病科
鼻子
外科
生物
环境卫生
遗传学
作者
Jijitha Lakshmanan,Karthikeyan Ramasamy,Arun Alexander,Sivaraman Ganesan
出处
期刊:Case Reports
[BMJ]
日期:2024-08-01
卷期号:17 (8): e256667-e256667
标识
DOI:10.1136/bcr-2023-256667
摘要
Sinonasal tumours of varying histology are not unusual in otolaryngology surgical practice. Juvenile angiofibroma (JAs) are vascular tumours usually occurring in adolescent male population; but rare in females. But similar clinical and radiological presentations are possible in females inducing strong suspicion of JA which needs to be ruled out by detailed evaluation. Here we present a case of a young female in her 20s who presented with a bleeding nasal mass which was finally diagnosed as sinonasal glomangiopericytoma which is a very rare sinonasal tumour. Tumours resembling JA do present in the female population but rarely turn out to be JA. A strong index of suspicion along with a handful of special blood investigations to rule out androgen insensitivity syndrome is mandatory.
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