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腋窝滑膜肉瘤复发累及臂丛神经,来自巴基斯坦的罕见病例报告

Axillary synovial sarcoma recurrence involving brachial plexus, a rare case report from Pakistan.

作者信息

Virji Safna Naozer, Pirzada Muhammad Ammar, Siddiqui Nadeem Ahmed, Idrees Romana, Zeeshan Sana

机构信息

Section of General Surgery, Department of Surgery, Aga Khan University Hospital, Karachi, Pakistan.

Section of Vascular Surgery, Department of Surgery, Aga Khan University Hospital, Karachi, Pakistan.

出版信息

Int J Surg Case Rep. 2023 Jun;107:108325. doi: 10.1016/j.ijscr.2023.108325. Epub 2023 May 19.

Abstract

INTRODUCTION

Synovial sarcomas are rare tumors, and the incidence of axillary synovial sarcoma involving the brachial plexus has been reported as 2.9 % among all axillary soft tissue tumors. However, the recurrence of axillary synovial sarcomas has not been reported in literature.

CASE PRESENTATION

A 36-years-old Afghan female presented in Karachi, Pakistan with a history of persistently increasing, recurrent, right axillary mass for 6 months. Initially diagnosed as a spindle-cell tumor on excision in Afghanistan, she had received ifosfamide and doxorubicin, but the lesion recurred. On examination, it was a 5 × 6 cm, hard mass palpable in right axilla. After radiological work-up and a multidisciplinary team discussion, she underwent complete excision of the tumor with successful preservation of brachial plexus. The final diagnosis was reported as monophasic synovial sarcoma FNCLCC Grade 3.

DISCUSSION

Our patient presented with a recurrent right axillary synovial sarcoma that was involving the axillary neurovascular bundle and brachial plexus, which was initially diagnosed as a spindle cell sarcoma. Pre-operative core-needle biopsy was unable to provide a definitive diagnosis. MRI scan was useful in delineating the proximity of the neurovascular structures. Re-excision of the tumor was performed which is the mainstay of treatment for axillary synovial sarcomas, combined with radiotherapy depending on the disease grading, staging and patient factors.

CONCLUSION

Axillary synovial sarcoma recurrence with involvement of the brachial plexus is an extremely rare presentation. Our patient was successfully managed through a multidisciplinary approach with complete surgical excision and preservation of the brachial plexus followed by adjuvant radiotherapy.

摘要

引言

滑膜肉瘤是罕见肿瘤,据报道,在所有腋窝软组织肿瘤中,累及臂丛神经的腋窝滑膜肉瘤发生率为2.9%。然而,腋窝滑膜肉瘤的复发情况在文献中尚未见报道。

病例介绍

一名36岁的阿富汗女性因右腋窝肿物持续增大、反复出现6个月就诊于巴基斯坦卡拉奇。该患者在阿富汗最初切除时被诊断为梭形细胞瘤,接受过异环磷酰胺和阿霉素治疗,但病变复发。查体发现右腋窝可触及一个5×6cm的硬肿块。经过影像学检查及多学科团队讨论后,她接受了肿瘤完整切除,成功保留了臂丛神经。最终诊断为单相性滑膜肉瘤,FNCLCC 3级。

讨论

我们的患者表现为复发性右腋窝滑膜肉瘤,累及腋窝神经血管束和臂丛神经,最初被诊断为梭形细胞肉瘤。术前粗针穿刺活检未能明确诊断。MRI扫描有助于确定神经血管结构的毗邻关系。对肿瘤进行了再次切除,这是腋窝滑膜肉瘤的主要治疗方法,并根据疾病分级、分期及患者因素联合放疗。

结论

腋窝滑膜肉瘤复发并累及臂丛神经是一种极其罕见的表现。我们的患者通过多学科方法成功治疗,完整手术切除并保留臂丛神经,随后进行辅助放疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da07/10225970/f2a37facefd4/gr1.jpg

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