Chaker Jaber, Khlas Ilyes, Bouassida Imen, Ayed Aymen Ben, Bousnina Mouna, Jmal Amine
Department of Cardiovascular Surgery, Abderrahmane Mami Hospital, Ariana, Tunisia.
Department of Thoracic Surgery, Abderrahmane Mami Hospital, Ariana, Tunisia.
Int J Surg Case Rep. 2024 Feb;115:109252. doi: 10.1016/j.ijscr.2024.109252. Epub 2024 Jan 12.
Synovial sarcoma is a malignant soft tissue tumor typically found near joints; its occurrence in the inguinal region is very rare.
We report a 23-years-old who presented with lower limb swelling. Imaging studies revealed a tumor in the groin area, compressing the femoral vein. A trucut biopsy concluded a synovial sarcoma. A complete resection was performed and the patient had adjuvant radiotherapy and chemotherapy with no evidence of reccurrence at 2-years follow-up.
Synovial sarcoma accounts for approximately 8 to 10 % of all soft tissue sarcomas. It is predominantly localized near the large joints in the limbs, with the inguinal location being extremely rare. Clinical diagnosis of the mass can sometimes be challenging. A needle biopsy, followed by histological analysis, is necessary to establish the diagnosis. MRI is considered the gold standard radiological examination for local staging of the tumor. The main treatment approach for synovial sarcoma is wide-margin resection, involving en-bloc resection of the tumor with clear margins. Vascular resection and reconstruction should be considered for involved vessels. Some authors argue that resection alone is sufficient for treating primary synovial sarcoma. However, adjuvant chemotherapy may be effective in cases where surgery quality is poor, making it a non-standard treatment. Others have highlighted the potential benefits of adjuvant radiotherapy, particularly in high-grade tumors.
Surgical excision remains the mainstay of treatment. Therefore, it is necessary to be aware of the different clinical presentations, which can sometimes be unusual.
滑膜肉瘤是一种恶性软组织肿瘤,通常发生在关节附近;其在腹股沟区的发生极为罕见。
我们报告一名23岁患者,出现下肢肿胀。影像学检查显示腹股沟区有一个肿瘤,压迫股静脉。粗针活检确诊为滑膜肉瘤。进行了完整切除,患者接受了辅助放疗和化疗,在2年随访中无复发迹象。
滑膜肉瘤约占所有软组织肉瘤的8%至10%。它主要局限于四肢的大关节附近,腹股沟部位极为罕见。对肿块进行临床诊断有时具有挑战性。需要进行针吸活检,随后进行组织学分析以确立诊断。MRI被认为是肿瘤局部分期的金标准影像学检查。滑膜肉瘤的主要治疗方法是广泛边缘切除,包括将肿瘤连同清晰边缘整块切除。对于受累血管应考虑进行血管切除和重建。一些作者认为单纯切除足以治疗原发性滑膜肉瘤。然而,辅助化疗在手术质量较差的情况下可能有效,使其成为一种非标准治疗。其他作者强调了辅助放疗的潜在益处,特别是在高级别肿瘤中。
手术切除仍然是主要的治疗方法。因此,有必要了解不同的临床表现,有时这些表现可能不寻常。