Bi Rui, Zhao Yan, Yang Wen-tao
Department of Pathology, Cancer Center, Fudan University; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China.
Department of Pathology, Taizhou People's Hospital, Taizhou 225300, China.
Zhonghua Bing Li Xue Za Zhi. 2013 Oct;42(10):660-4.
To study the clinicopathologic characteristics of mitotically active cellular fibroma (MACF) of the ovary.
The clinicopathologic features of 11 cases of MACF from 2008 to 2012 years were retrospectively reviewed and immunohistochemic EnVision method was performed.
The age of patients ranged from 21 to 65 years (mean = 46 years). The maximum tumor diameter varied from 6 to 16 cm (mean = 9.8 cm). The tumors were densely cellular and composed of intersecting bundles of spindle cells, sometimes associated with storiform pattern. The mitotic count ranged from 4 to 20 per 10 high-power field (mean = 8.4). Atypical mitotic figures were not identified and coagulative tumor necrosis was not found. There was at most mild to moderate degree of nuclear atypia. Immunohistochemically, 8 cases showed positive stain for vimentin and 5 cases expressed diffusely or focally WT-1. In 6 cases, Ki-67 positive index ranged from 5%-30%, including 1 case (10%), and 1 case (30%) in which mitotic figures were 20/10 HPF. CK,AE1/AE3, CD117, CD34, CD99 and desmin were negative in the detected 5 cases. Reticular fiber staining in 2 cases showed dense reticular fibers enveloping individual tumor cells. Ten patients who followed-up range from 4 to 38 months were alive without evidence of recurrence or disease progression. One patient was alive with local recurrence 94 months after surgery.
Cellular fibromatous neoplasm with mitotic count of ≥ 4/10 HPF but relatively bland nuclear features should be considered as MACF rather than ovarian fibrosarcoma. MACF is a group of ovarian tumor which carries a low malignant potential and occasional chance of recurrence.
研究卵巢有丝分裂活跃性细胞性纤维瘤(MACF)的临床病理特征。
回顾性分析2008年至2012年期间11例MACF的临床病理特征,并采用免疫组织化学EnVision法检测。
患者年龄21至65岁(平均46岁)。肿瘤最大直径6至16厘米(平均9.8厘米)。肿瘤细胞密集,由梭形细胞相互交织的束状结构组成,有时伴有席纹状结构。每10个高倍视野有丝分裂数为4至20个(平均8.4个)。未发现非典型有丝分裂象,也未发现凝固性肿瘤坏死。核异型性至多为轻度至中度。免疫组织化学检测,8例波形蛋白染色阳性,5例WT-1弥漫或局灶性表达。6例中,Ki-67阳性指数为5%至30%,其中有丝分裂数为20/10 HPF的分别有1例(10%)和1例(30%)。所检测的5例中,细胞角蛋白、AE1/AE3、CD117、CD34、CD99和平滑肌肌动蛋白均为阴性。2例网状纤维染色显示密集的网状纤维包绕单个肿瘤细胞。随访4至38个月的10例患者存活,无复发或疾病进展迹象。1例患者术后94个月局部复发存活。
有丝分裂数≥4/10 HPF但核特征相对温和的细胞性纤维瘤性肿瘤应考虑为MACF而非卵巢纤维肉瘤。MACF是一组具有低恶性潜能和偶有复发机会的卵巢肿瘤。