Bilateral inflammatory myofibroblastic tumor mastoiditis

被引:5
作者
Rodgers, Brian [1 ]
Bhalla, Vidur [1 ]
Zhang, Da [2 ]
El Atrouni, Wissam [3 ]
Wang, Fen [4 ]
Sundararajan, Jayashree [5 ]
Lin, James [1 ]
机构
[1] Univ Kansas Hosp, Dept Otolaryngol Head & Neck Surg, Kansas City, KS USA
[2] Univ Kansas Hosp, Dept Pathol & Lab Med, Kansas City, KS USA
[3] Univ Kansas Hosp, Dept Infect Dis, Kansas City, KS USA
[4] Univ Kansas Hosp, Dept Radiat Oncol, Kansas City, KS USA
[5] Univ Kansas Hosp, Dept Neurol, Kansas City, KS USA
来源
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK | 2015年 / 37卷 / 11期
关键词
inflammatory myofibroblastic tumor; bilateral mastoiditis; sigmoid sinus thrombosis; facial nerve paralysis; inflammatory pseudotumor; TEMPORAL BONE; PSEUDOTUMOR; HEAD; NECK; CELLS;
D O I
10.1002/hed.23978
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background. Inflammatory myoblastic tumors (IMTs) are rare, mesenchymal neoplasms most commonly located in areas of previous inflammation. In the temporal bone, these tumors typically present as solitary, space-occupying lesions that clinically resemble chronic otitis media. Methods. We present a case of bilateral IMTs with facial nerve involvement, sigmoid sinus thrombosis, leptomeningeal enhancement, and seizures. Results/Conclusion. This case demonstrates the need for a high index of suspicion of IMT when imaging reveals bilateral mastoid opacification. These tumors are more aggressive than their orbital counterparts and require multimodality therapy to prevent recurrence and alleviate severe neurotologic symptoms. (C) 2015 Wiley Periodicals, Inc.
引用
收藏
页码:E142 / E145
页数:4
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