卵巢纤维肉瘤病例报告

Julia Akhter Nira
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摘要

卵巢纤维肉瘤是一种极为罕见的卵巢恶性性索间质瘤,是一种由良性纤维瘤肿瘤恶变而来的新发或继发肿瘤。截至今天,全世界报告的病例总数不超过100例,没有明确的诊断标准、预后因素和治疗方式。通常表现为单侧实体瘤。它可以发生在任何年龄,尽管绝经后的诊断更频繁。大多数患者表现为模糊的腹痛和卵巢引起的下腹部肿块。超声检查通常显示卵巢单侧实体性同质肿瘤,回声增强不均匀,血管增加。血清肿瘤标志物和性激素如CA-125通常在正常水平内发现。术前冷冻切片研究往往得出错误诊断的结论,术后组织病理学诊断通常显示梭形细胞具有较高的有丝分裂活性,背景为纤维组织。根据有丝分裂活性,即与出血和坏死相关的细胞异型性,它与有丝分裂活动的良性纤维瘤区分开来。免疫组化结果可能是阳性的波形蛋白,α-抑制素,SMA,雌激素受体,孕激素受体。Ki-67阳性率与恶性肿瘤的严重程度,即分级和预后有关。我们的病例具有上述特征,术后通过组织学和组织化学证实,Vimentin和Ki-67阳性。由于没有足够的病例来得出最终的治疗方案,到目前为止,接受治疗的病例显示,全细胞减灭术后再进行术后化疗具有更好的预后。在卵巢纤维肉瘤的鉴别诊断中,应采用圆形、实心的单侧异质性卵巢肿瘤。由于这是一种极为罕见的卵巢肿瘤,通常没有特异性肿瘤标志物的升高,目前也没有结论性的诊断标准,涉及多中心方法的临床研究与分子水平的研究相结合是妇科医生未来更好地诊断和治疗的首要要求。J Bangladesh Coll Phys Surg 2023;41:89-92
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Case Report - Fibrosarcoma of Ovary
  Fibrosarcoma of ovary, a tumour arising do novo or secondary to malignant transformation of benign fibromatous tumours, is an extremely rare malignant sex cord stromal tumour of ovary. As on today, the total number of reported cases throughout the world is not more than hundred, There is no clearcut diagnostic criteria, prognostic factor and treatment modalities. Usually it presents as unilateral solid tumour. It can occur at any age though postmenopausal diagnosis is more frequent. Majority of the patients present with vague abdominal pain and a lump in lower abdomen arising from ovary. Ultrasonographic findings usually reveals unilateral solid homogenous tumour in ovary with uneven echo enhancement and increased vascularity. Serum tumor markers and sex hormones such as CA-125 usually found within normal levels. Peroperative frozen section study often concludes into wrong diagnosis, postoperative histopathological diagnosis usually reveals spindle cells with high mitotic activity with  Background of fibrous tissue. Depending on mitotic activity, cellular atypia associated with haemorhage and necrosis, it is differentiated from benign fibroma with mitotic activity. Immunohistochemistry findings may be positive for vimentin, á-inhibin, SMA, estrogen receptor, progesterone receptor. Ki-67 positive rate is associated with degree of severity of malignancy i.e, grading and prognosis. Our case was having the above features and was confirmed postoperatively by histological and later by histochemistry with positive Vimentin and Ki-67. As there were not enough cases to conclude a final treatment protocol, so far treated cases revealed total cytoreductive surgery followed by postoperative chemotherapy has the better prognosis. A round, solid unilateral heterogenous ovarian tumor should be taken in differential diagnosis of ovarian fibrosarcoma. As this is an extremely rare tumour of the ovary, there is usually no rise of specific tumuor marker, no conclusive diagnostive criteria available at present, clinical studies involving multicentered approach associated with studies at molecular level is a prime requirement for the gynaecologist to diagnose and treat in a better way in future. J Bangladesh Coll Phys Surg 2023; 41: 89-92
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