Abdessayed Nihed, Barka Malek, Mabrouk Samiha, Nfikha Zeineb, Maatoug Zeineb, Fejji Yosra, Jarrar Mohamed Salah, Youssef Sabri, Mokni Moncef
Department of Pathology, Farhat Hached University Hospital, Sousse, Tunisia.
Research Lab: Transfer in Technology in Anatomic Pathology (LR12SP08), Sousse, Tunisia.
Surg Case Rep. 2023 Sep 6;9(1):158. doi: 10.1186/s40792-023-01744-2.
Synovial sarcoma is an uncommon soft tissue malignancy that mainly occurs near tendon sheath and bone joints. Primary intra-abdominal location is exceedingly rare and characterized by non-specific clinical signs.
We report the case of a young female without medical history who presented with acute abdominopelvic pain. Ultrasound echography revealed a right mass measuring 7 cm in greater diameter cystic with solid areas, likely of ovarian origin. A coelioscopy with peritoneal biopsies was performed. Histological examination with immunohistochemistry concluded the diagnosis of GIST. The patient was referred to the surgery department and after laboratory routine analysis and computed tomography, the patient was proposed to surgical management. Per-operative findings revealed a mesenteric mass locally invading the greater omentum and the appendicular wall. Pathological examination with immunochemistry confirmed the diagnosis of mesenteric monophasic synovial sarcoma invading the appendicular wall with positive surgical margins. Chemotherapy was proposed with a good response. Our patient is free from disease 9 months later.
We aimed through this case report to discuss mesenteric presentation monophasic SS, mimicking ovarian malignancy, emphasizing clinicopathological features and differential diagnoses.
滑膜肉瘤是一种罕见的软组织恶性肿瘤,主要发生在腱鞘和骨关节附近。原发性腹腔内滑膜肉瘤极为罕见,临床症状不具特异性。
我们报告一例无病史的年轻女性,因急性腹盆腔疼痛就诊。超声检查发现右侧有一肿块,最大直径7厘米,呈囊实性,可能起源于卵巢。进行了腹腔镜检查及腹膜活检。免疫组织化学的组织学检查确诊为胃肠道间质瘤(GIST)。患者被转至外科,经实验室常规分析和计算机断层扫描后,拟行手术治疗。术中发现肠系膜肿块局部侵犯大网膜和阑尾壁。免疫组织化学病理检查确诊为肠系膜单相滑膜肉瘤侵犯阑尾壁,手术切缘阳性。建议进行化疗,患者反应良好。9个月后,患者无疾病迹象。
我们通过本病例报告旨在探讨模仿卵巢恶性肿瘤的肠系膜单相滑膜肉瘤的表现,强调其临床病理特征和鉴别诊断。