Primary extraskeletal Ewing sarcoma of the sinonasal tract: a rare case report and review of the literature

被引:0
作者
Yao, Li-Ding [1 ]
Tang, Jin-Long [2 ]
Lu, Liang-Ji [1 ]
Sayfoo, Mohammad-Farez [3 ]
Zhu, Xiu-Liang [1 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 2, Sch Med, Dept Radiol, 88 Jiefang Rd, Hangzhou 310009, Zhejiang, Peoples R China
[2] Zhejiang Univ, Affiliated Hosp 2, Sch Med, Dept Pathol, 88 Jiefang Rd, Hangzhou 310009, Zhejiang, Peoples R China
[3] Zhejiang Univ, Sch Med, 866 Yuhangtang Rd, Hangzhou 310058, Zhejiang, Peoples R China
关键词
Ewing sarcoma; extraskeletal; sinonasal tract; PRIMITIVE NEUROECTODERMAL TUMOR; MAXILLARY SINUS; METASTATIC PATTERNS; IMAGING FEATURES; ETHMOID SINUS; ADULTS; FAMILY; DISEASE; NECK; HEAD;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Purpose: Extraskeletal Ewing sarcoma (EES) is a rare, round-cell malignant neoplasm that mostly manifests as a large and bulky soft-tissue mass. EES is most commonly found in the paravertebral region, extremities, chest wall, retroperitoneum, pelvis and hip. EES can occur in the head and neck. However such locations are considered to be rare for this type of malignant neoplasm. Methods: We report a 41 years female diagnosed with EES, and performed a brief review about the clinical features and diagnostic strategies of the EES. Results: The CT and MRI examination reveals a mass in the nasal cavity and paranasal sinuses, and the pathological examination supported the diagnosis of EES. Conclusions: Primary Ewing's sarcoma must be considered when the expansile nasal mass is detected with extensive invasion into adjacent structures and bony destructive changes, although which is a very rare condition.
引用
收藏
页码:5256 / 5262
页数:7
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