Isolated Infratemporal Fossa Desmoid Fibromatosis: A Rare Case Report and Review of Literature.

孤立性颞下窝纤维瘤病 ：罕见病例报告及文献复习.

• 发表时间: Oct 2022
• 来源期刊: Indian J Otolaryngol Head Neck Surg
• DOI: 10.1007/s12070-020-02294-x
• PMID: 36452559
• 文章类型: Journal Article
• 作者列表: Munnangi A,Kadapathri A,Pillai V,Bhat S,Rajeswarie RT,Shetty V,Subramanium N,Kolur T,Bhushan R V

关键词: Aggressive fibromatosis; Desmoid tumor; Endoscopic; Infratemporal fossa; Mandibulotomy; Pediatric

Abstract

Desmoid fibromatosis (DF) arising from musculoaponeurotic structures rarely affects the head and neck region with the abdomen being the most common site of origin. These are benign tumors with locally infiltrative nature usually presenting as painless swellings that are rapidly growing. The infratemporal fossa DF is an extremely rare location with few clinical reports. This article discusses the management of a 2-year-old child with DF of the infratemporal fossa (ITF) along with literature review.

摘要

由肌筋膜结构引起的纤维瘤病（DF）很少影响头颈部，腹部是最常见的起源部位。这些是具有局部浸润性的良性肿瘤，通常表现为快速生长的无痛肿胀。颞下窝DF是极为罕见的位置，临床报道很少。本文讨论了2岁儿童的颞下窝DF（ITF）的管理以及文献综述。