首页> 外文期刊>Pathology Research and Practice >Two cases of supernumerary ovary: one with large fibroma with Meig's syndrome and the other with endometriosis and cystic change.
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Two cases of supernumerary ovary: one with large fibroma with Meig's syndrome and the other with endometriosis and cystic change.

机译:宫外卵巢有2例:1例患有Meig综合征的大纤维瘤,另一例伴有子宫内膜异位和囊性变。

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Reports of supernumerary ovaries are rare. We describe two such cases, one with fibroma and the other with endometriosis and cystic change. A large fibroma measuring 17.4 x 12.0 x 7.5 cm in size was found in the supernumerary ovary of the omentum in the first case of a 47-year-old married woman with Meig's syndrome. The second case was associated with endometriosis and cystic change, measuring 11 x 5 x 3 cm in size and located in the upper abdominal cavity. It was attached to the uterus of a 28-year-old pregnant woman who had neither fibroma nor Meig's syndrome. Histologically, corpus albicans and a few primordial germ cells were demonstrated, respectively. A fibroma showing a storiform pattern was found in the first case. The second case had endometriosis and a thin-walled cyst with bleeding and necrosis caused by torsion. Immunohistochemically, desmin, alpha-smooth muscle actin, c-kit, CA125, Na+/K+ATPase, overexpression of p53, myc and ras were all negative in the fibroma cells of the first case, and in the endometriosis and cyst wall of the second case. The fibroma cells were positive for vimentin and estrogen receptor, and the proliferating cell nuclear antigen was sporadically demonstrated in their nuclei. The mutation of the p53 gene at exons 5-8 was not detected by sequence analysis. Using RT-PCR, bax, bcl-2 and p16 were not detected either. Clinically, the two cases presented here did not show abnormal hormonal symptoms. They were diagnosed as abdominal tumors or masses. Based on these considerations, one might assume that supernumerary ovaries are probably more frequent than reported at present.
机译:关于卵巢过多的报道很少。我们描述了两种情况,一种是纤维瘤,另一种是子宫内膜异位和囊性变。在一名患有Meig综合征的47岁已婚妇女的第一例病例中,大网膜卵巢中发现了一个尺寸为17.4 x 12.0 x 7.5 cm的大纤维瘤。第二例与子宫内膜异位和囊性改变有关,大小为11 x 5 x 3 cm,位于上腹腔。它附着在一名既没有纤维瘤也没有Meig综合征的28岁孕妇的子宫上。在组织学上,分别证明了白色bic体和一些原始生殖细胞。在第一种情况下,发现纤维瘤呈星形状。第二例患有子宫内膜异位症和一个薄壁的囊肿,其扭曲引起出血和坏死。免疫组织化学检查,结蛋白,α-平滑肌肌动蛋白,c-kit,CA125,Na + / K + ATPase,p53,myc和ras的过表达在第一种情况的纤维瘤细胞以及子宫内膜异位和囊肿壁均阴性。第二种情况。纤维瘤细胞对波形蛋白和雌激素受体呈阳性,并在其细胞核中偶尔显示出增殖的细胞核抗原。通过序列分析未检测到外显子5-8处p53基因的突变。使用RT-PCR,也未检测到bax,bcl-2和p16。临床上,这里介绍的两个病例没有显示出异常的荷尔蒙症状。他们被诊断为腹部肿瘤或肿块。基于这些考虑,人们可能会认为多余的卵巢可能比目前报道的更为频繁。

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