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

被引:1
|
作者
Munnangi, Ashwini [1 ]
Kadapathri, Abhimanyu [1 ]
Pillai, Vijay [1 ]
Bhat, Sunil [2 ]
Rajeswarie, R. T. [3 ]
Shetty, Vivek [1 ]
Subramanium, Narayana [1 ]
Kolur, Trupti [1 ]
Bhushan, R. Vidya [1 ]
机构
[1] Mazumdar Shaw Canc Ctr, Head & Neck Oncol, Bangalore, Karnataka, India
[2] Mazumdar Shaw Canc Ctr, Pediat Hematol Oncol, Bangalore, Karnataka, India
[3] Mazumdar Shaw Canc Ctr, Pathol, Bangalore, Karnataka, India
关键词
Aggressive fibromatosis; Desmoid tumor; Pediatric; Infratemporal fossa; Endoscopic; Mandibulotomy; PEDIATRIC AGGRESSIVE FIBROMATOSIS; METHOTREXATE; TUMORS; NECK; HEAD; CHEMOTHERAPY; VINBLASTINE; CHILDREN;
D O I
10.1007/s12070-020-02294-x
中图分类号
R61 [外科手术学];
学科分类号
摘要
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.
引用
收藏
页码:2609 / 2613
页数:5
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