翼腭窝孤立性纤维性肿瘤1例报告及文献复习。

IF 2.2
Jian-Sheng Zhou, Hui Yuan, Jiu-Qiang Chen, Lei Shen
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引用次数: 0

摘要

单发纤维性肿瘤是一种罕见的梭形细胞肿瘤,可发生在身体的各个部位。在翼腭窝中未见单发纤维性肿瘤的报道。病例报告:25岁男性,自诉右侧面部麻木20天。鼻窦的计算机断层扫描显示以右侧翼腭窝为中心的边界清晰的病变。磁共振成像T1加权成像(T1WI)病变与肌肉呈均匀等强,T2加权成像(T2WI)病变与肌肉呈轻微高强度。术中冷冻病理显示为良性梭形细胞瘤。经鼻联合Caldwell-Luc入路成功切除肿瘤,无并发症。最终病理结合免疫组化证实为孤立性纤维性肿瘤。术后无进一步放疗。随访半年,无复发。结论:翼状腭窝肿瘤应考虑单发纤维性肿瘤的可能性,内镜下根治性切除为首选治疗方法。
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 pterygopalatine fossa: a rare case report and literature review.

Introduction: Solitary fibrous tumor is a rare spindle cell tumor that may occur in various parts of the body. No documented case of solitary fibrous tumor has been reported in pterygopalatine fossa.

Case report: A 25-year-old male complained of right facial numbness for 20 days. Computed tomography of the paranasal sinuses demonstrated a well-circumscribed lesion centered in the right pterygopalatine fossa. On magnetic resonance imaging the lesion was homogenously isointense to muscle on T1 weighted imaging (T1WI) and slightly hyperintense to muscle on T2 weighted (T2WI). The intro-operative frozen pathology reveals a benign spindle cell tumor. The tumor was removed successfully via transnasal combined with Caldwell-Luc approach without complications. However, the final pathology combined with immunohistochemistry confirmed the diagnosis of solitary fibrous tumor. No further radiotherapy is performed post-operation. After half a year follow up, there is no recurrence.

Conclusion: For the tumor in the pterygopalatine fossa, the possibility of solitary fibrous tumor should be considered and radical endoscopic resection should be the preferred treatment approach.

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