Spindle Cell Sarcoma of the Maxilla: A Rare Entity, Case Report, and Review of the Literature

被引:3
|
作者
Schwitzer, David [1 ]
Kim, Roderick [2 ,3 ]
Williams, Fayette [3 ]
Hammer, Daniel [3 ]
机构
[1] Parkland Mem Hosp & Affiliated Inst, UT SouthWestern Med Ctr, Dept Oral & Maxillofacial Surg, 5323 Harry Hines Blvd,CS3-104, Dallas, TX 75390 USA
[2] John Peter Smith Hosp, Res, Ft Worth, TX 76104 USA
[3] John Peter Smith Hosp, Div Maxillofacial Oncol & Reconstruct Surg, Ft Worth, TX 76104 USA
关键词
RADIATION-THERAPY; SOFT-TISSUE; HEAD; CARCINOMA; FEATURES; SINUS;
D O I
10.1016/j.joms.2020.02.003
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Spindle cell sarcoma (SCS) is a malignancy, with the most recent Surveillance, Epidemiology, and End Results (SEER) data citing a total of 250 reported cases occurring in the head and neck. Of these cases, none originated in the maxillofacial hard tissue. To the best of our knowledge, only 2 cases of primary osseous SCS of the maxillofacial region have been reported. These cases were not accounted for in the SEER data. The diagnosis of SCS requires its differentiation from other sarcomas and spindle cell neo-plasms. Therefore, a comprehensive review to reinforce its inclusion in oral and maxillofacial surgeons' differential diagnosis for osseous neoplastic pathology is desired. In the present case report, we have described a maxillary SCS in a patient with an initial diagnosis of a spindle cell lesion of uncertain biologic behavior. We reviewed the data for SCS, including the epidemiologic data, diagnostic challenges, clinical and radiographic presentations, prognostic indicators, and treatment. (C) 2020 American Association of Oral and Maxillofacial Surgeons
引用
收藏
页码:1334 / 1342
页数:9
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