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一名54岁女性筛窦原发性滑膜肉瘤的罕见表现:病例报告及文献综述

An unusual presentation of primary synovial sarcoma of the ethmoid sinus in a 54-year-old woman: A case report and literature review.

作者信息

Abdul-Hafez Hamza A, Abu-Alrub Reem A, Barakat Mohammed A, Meri Ahmad Ziad, Rass Hanood Abu

机构信息

Department of Medicine, Faculty of Medicine and Health Sciences, An-Najah National University, Nablus, Palestine.

Department of Medicine, Faculty of Medicine and Health Sciences, An-Najah National University, Nablus, Palestine.

出版信息

Int J Surg Case Rep. 2025 Jan;126:110784. doi: 10.1016/j.ijscr.2024.110784. Epub 2024 Dec 26.

Abstract

INTRODUCTION AND IMPORTANCE

Synovial sarcoma is a malignant soft tissue tumor primarily affects the extremities. Its presence in the paranasal sinuses, especially within the ethmoid sinus, is exceedingly rare.

CASE PRESENTATION

We report a case of monophasic synovial sarcoma of the ethmoid sinus in a 54-year-old woman, who presented with 3 months history of left eye pain and bulging. CT with contrast, MRI, and histopathology confirmed the diagnosis. Whose management was partial surgical resection with postoperative chemotherapy and radiotherapy. Post-treatment, the patient showed a good clinical outcome and remained under regular follow-up care by the oncology team.

CASE DISCUSSION

To our knowledge, there are only six reported cases of primary synovial sarcoma in the ethmoid sinus. Its atypical presentation and unspecific features make diagnosis challenging. Partial surgical resection with postoperative chemotherapy and radiotherapy is the standard treatment. However, the prognosis remains poor, with a high risk of recurrence, necessitating thorough follow-up.

CONCLUSION

This case highlights the presentation and management of a significantly rare tumor in unusual body region.

摘要

引言与重要性

滑膜肉瘤是一种主要累及四肢的恶性软组织肿瘤。它在鼻窦,尤其是筛窦内出现极为罕见。

病例介绍

我们报告一例54岁女性筛窦单相滑膜肉瘤病例,该患者有3个月左眼疼痛和眼球突出病史。增强CT、MRI及组织病理学确诊了该诊断。其治疗为部分手术切除,术后进行化疗和放疗。治疗后,患者临床结局良好,仍在肿瘤团队的定期随访护理之下。

病例讨论

据我们所知,仅有6例筛窦原发性滑膜肉瘤的报道病例。其非典型表现和非特异性特征使得诊断具有挑战性。部分手术切除联合术后化疗和放疗是标准治疗方法。然而,预后仍然较差,复发风险高,需要进行全面随访。

结论

本病例突出了在不寻常身体部位一种极为罕见肿瘤的表现及治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc0/11743864/f008fabc12c7/gr1.jpg

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