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蝶窦内黏液瘤的罕见表现:病例报告及文献复习

The Unusual Presentation of a Myxoma Within the Sphenoid Sinus: Case Report and Review of the Literature.

作者信息

Clarke Julian V, Mandpe Aditi H, Weber Peter B, Vogel Hannes, Leng Lewis Z

机构信息

Washington University School of Medicine, St. Louis, Missouri, USA.

Department of Otolaryngology-Head and Neck Surgery, California Pacific Medical Center, San Francisco, California, USA.

出版信息

World Neurosurg. 2017 Jul;103:951.e5-951.e12. doi: 10.1016/j.wneu.2017.04.019. Epub 2017 Apr 20.

Abstract

BACKGROUND

We describe a rare case of a sphenoid sinus myxoma that was resected via an endoscopic endonasal skull base approach. We review the literature regarding these rare tumors of the paranasal sinuses.

CASE DESCRIPTION

A 72-year-old woman was diagnosed with an incidental sphenoid sinus tumor and left sphenoid wing meningioma during a workup for left-sided proptosis and diplopia. Biopsies of the sphenoid wing and sphenoid sinus tumors were obtained. After undergoing surgical resection of the meningioma, the patient then underwent definitive resection of the sphenoid sinus myxoma via endoscopic endonasal skull base approach. Postoperative imaging demonstrated a gross total resection. The patient suffered postoperative thromboembolic complications due to underlying hypercoagulable state but made a complete recovery and returned to her neurologic baseline. There has been no evidence of recurrent myxoma in the sphenoid sinus 24 months after surgery.

DISCUSSION

Myxomas are benign tumors derived from primitive mesenchyme. Myxomas very rarely present in the paranasal or skull base location. Complete surgical resection is the primary treatment for these tumors. The endoscopic endonasal approach is an effective technique for resecting various benign and more aggressive extradural skull base tumors.

CONCLUSIONS

Myxomas of the sphenoid sinus are rare. The endoscopic endonasal skull base approach is an effective and minimal access technique for resection of this rare tumor of the sphenoid sinus.

摘要

背景

我们描述了一例罕见的蝶窦黏液瘤,通过鼻内镜经鼻颅底入路进行了切除。我们回顾了关于这些罕见鼻窦肿瘤的文献。

病例描述

一名72岁女性在因左侧眼球突出和复视进行检查时,被诊断出偶然发现蝶窦肿瘤和左侧蝶骨嵴脑膜瘤。获取了蝶骨嵴和蝶窦肿瘤的活检样本。在接受脑膜瘤手术切除后,患者随后通过鼻内镜经鼻颅底入路对蝶窦黏液瘤进行了根治性切除。术后影像学检查显示肿瘤全切。患者因潜在的高凝状态出现了术后血栓栓塞并发症,但完全康复并恢复到神经功能基线水平。术后24个月,蝶窦未见黏液瘤复发迹象。

讨论

黏液瘤是源自原始间充质的良性肿瘤。黏液瘤极少出现在鼻窦或颅底部位。完整的手术切除是这些肿瘤的主要治疗方法。鼻内镜经鼻入路是切除各种良性及更具侵袭性的硬膜外颅底肿瘤的有效技术。

结论

蝶窦黏液瘤罕见。鼻内镜经鼻颅底入路是切除这种罕见蝶窦肿瘤的一种有效且微创的技术。

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