颞肌孤立性纤维瘤1例报告并文献复习。

Q2 Medicine
Archives of Craniofacial Surgery Pub Date : 2023-10-01 Epub Date: 2023-10-20 DOI:10.7181/acfs.2023.00199
Jun Ho Choi, Soo Hyuk Lee, Jae Ha Hwang, Kwang Seog Kim, Sam Yong Lee
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引用次数: 0

摘要

孤立性纤维瘤(SFT)是一种罕见的肿瘤,最常见于胸膜,但偶尔也会在头颈部发展。然而,没有报道描述颞肌中的SFT。在此,我们提出了第一个已知的颞肌SFT病例。一名47岁的男子抱怨他的右太阳穴有一个无痛的明显肿块。面部增强计算机断层扫描在颧骨弓下的右侧颞肌发现一个4.0×2.9×1.4厘米的肿块,表现为血管肿瘤。在全身麻醉下从右侧颞肌切除肿块。组织病理学检查显示肿块为SFT。术后无并发症发生,包括功能障碍或感觉丧失。患者随访3个月,无并发症。尽管肺外区域的SFT很少见,但在颞叶区域肿块的鉴别诊断中应该考虑它。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Solitary fibrous tumor in the temporalis muscle: a case report and literature review.

Solitary fibrous tumor in the temporalis muscle: a case report and literature review.

Solitary fibrous tumor in the temporalis muscle: a case report and literature review.

Solitary fibrous tumor in the temporalis muscle: a case report and literature review.

Solitary fibrous tumor (SFT) is an infrequently occurring neoplasm most commonly observed in the pleura, but it can develop in the head and neck region in occasional cases. However, no reports have described SFT in the temporalis muscle. Herein, we present the first known case of SFT in the temporalis muscle. A 47-year-old man complained of a painless palpable mass on his right temple. Facial enhanced computed tomography identified a 4.0× 2.9× 1.4 cm mass presenting as a vascular tumor in the right temporalis muscle under the zygomatic arch. The mass was excised from the right temporalis muscle under general anesthesia. A histopathologic examination revealed that the mass was an SFT. No complications occurred after surgery, including functional disability or sensory loss. The patient was followed up for 3 months without complications. Although SFT in extrapulmonary regions is rare, it should be considered in the differential diagnosis of masses that occur in the temporal area.

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来源期刊
Archives of Craniofacial Surgery
Archives of Craniofacial Surgery Medicine-Otorhinolaryngology
CiteScore
2.90
自引率
0.00%
发文量
44
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