Sharabati Haneen H, Innab Laila R, Hussein Saja S, Salman Ayman A, Naser Anis M, Bakri Izzeddin A
Al Quds University Faculty of Medicine, Jerusalem, Palestine.
Department of Neurosurgery, Al-Makassed Islamic Charitable Hospital, Jerusalem 00970, Palestine.
J Surg Case Rep. 2024 Oct 2;2024(10):rjae579. doi: 10.1093/jscr/rjae579. eCollection 2024 Oct.
Synovial sarcomas are rare soft tissue tumors primarily affecting the extremities but can occasionally manifest in unusual locations such as the ethmoid sinus, posing diagnostic challenges. We present a case of a 38-year-old male with a 7-month history of recurrent throbbing headaches, left eye pain, and facial nerve palsy, evolving into multiple stroke episodes. Radiological studies showed extension to the cavernous sinus, raising an initial suspicion of vasculitis. Histological findings of an endoscopic biopsy, however, confirmed a monophasic synovial sarcoma. The patient was referred to a specialized center for further management. Unfortunately, he developed another stroke before receiving treatment. Management included chemotherapy and definitive radiation therapy targeting the ethmoid sinus. The patient is currently receiving ongoing palliative care for symptom management. This case underscores the importance of early diagnosis and a multidisciplinary approach in managing rare and aggressive tumors such as synovial sarcoma of the ethmoid sinus.
滑膜肉瘤是一种罕见的软组织肿瘤,主要累及四肢,但偶尔也会出现在不寻常的部位,如筛窦,这给诊断带来了挑战。我们报告一例38岁男性,有7个月反复搏动性头痛、左眼疼痛和面神经麻痹病史,随后发展为多次中风发作。影像学研究显示肿瘤已蔓延至海绵窦,最初怀疑为血管炎。然而,内镜活检的组织学结果证实为单相滑膜肉瘤。该患者被转诊至专科中心进行进一步治疗。不幸的是,他在接受治疗前又发生了一次中风。治疗包括化疗和针对筛窦的根治性放射治疗。该患者目前正在接受持续的姑息治疗以控制症状。本病例强调了早期诊断和多学科方法在管理罕见且侵袭性肿瘤(如筛窦滑膜肉瘤)中的重要性。