Mraihi Fathi, Basly Jihene, Slama Feryal, Azouz Eya, Ayari Asma, Chelli Dalenda
D Department at the Maternal Center of Tunis, Tunis, Tunisia.
D Department at the Maternal Center of Tunis, Tunis, Tunisia.
Int J Surg Case Rep. 2023 Nov;112:108938. doi: 10.1016/j.ijscr.2023.108938. Epub 2023 Oct 10.
Ovarian fibrosarcoma is a rare cancer. In the literature, there have been very few occurrences of fibrosarcoma with ascites. The presence of ascites complicates the diagnosis further, and is associated with a poor prognosis and has been linked to chemoresistance and metastasis. We present this case of an ovarian fibrosarcoma with ascites to provide a comprehensive overview of the clinical presentation, diagnostic evaluation and management of this pathology, which remains a challenge given the rarity of this entity.
We report the case of a 60-year-old woman who was referred to our unit, because of abdominal bloating, sporadic pelvic pain and abdominal distension. Ultrasound showed a heterogeneous mass over the right adnexa with ascites. Serum tumour markers were within normal limits. During surgery, a total abdominal hysterectomy plus bilateral adnexectomy was performed. The final histopathological findings showed a well-differentiated fibrosarcoma. The patient was followed up regularly and no recurrence was seen 2 years after surgery.
Ovarian fibrosarcomas are uncommon cancers with no known risk factors. Diagnosis can be difficult, especially in the presence of ascites, and other diagnostic options should be considered. Pathological and immunohistochemistry investigations are required for a clear diagnosis. Early metastases and resistance to adjuvant chemotherapy characterize the prognosis of ovarian fibrosarcoma with ascites.
Ovarian fibrosarcoma with ascites is a rare and challenging ovarian disease, highlighting the need for postoperative pathology to make a clear diagnosis, complete cytoreductive surgery and individual consideration of adjuvant radiochemotherapy should be included in the management.
卵巢纤维肉瘤是一种罕见的癌症。在文献中,伴有腹水的纤维肉瘤病例极少。腹水的存在使诊断进一步复杂化,与预后不良相关,并与化疗耐药和转移有关。我们呈现这例伴有腹水的卵巢纤维肉瘤病例,以全面概述这种病理情况的临床表现、诊断评估和管理,鉴于该实体的罕见性,这仍然是一项挑战。
我们报告一例60岁女性病例,该患者因腹胀、散发性盆腔疼痛和腹部膨隆被转诊至我院。超声检查显示右侧附件区有一不均质肿块伴腹水。血清肿瘤标志物在正常范围内。手术中,进行了全腹子宫切除术加双侧附件切除术。最终组织病理学检查结果显示为高分化纤维肉瘤。患者接受定期随访,术后2年未见复发。
卵巢纤维肉瘤是罕见的癌症,尚无已知的危险因素。诊断可能困难,尤其是在有腹水的情况下,应考虑其他诊断方法。明确诊断需要进行病理和免疫组织化学检查。早期转移和对辅助化疗的耐药是伴有腹水的卵巢纤维肉瘤预后的特征。
伴有腹水的卵巢纤维肉瘤是一种罕见且具有挑战性的卵巢疾病,强调需要术后病理以明确诊断,管理中应包括完整的肿瘤细胞减灭术和对辅助放化疗的个体化考虑。