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Primary retroperitoneal mucinous cystadenocarcinoma with mural nodules: A case report and literature review

机译:原发性腹膜后黏液性囊腺癌伴壁瘤:一例报道并文献复习

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摘要

A primary retroperitoneal mucinous cystadenocarcinoma (PRMC) is an extremely rare lesion. To date, only 49 cases have been reported. The presence of mural nodules in a PRMC may indicate a worse prognosis. We report the case of a 40-year-old Japanese woman with a PRMC with mural nodules. Microscopic examination revealed that the stromal cells of the nodules were spindleshaped and varied in size. The nodules were immunoreactive for vimentin but negative for cytokeratin and EMA, and the nuclei of the stromal cells were pleomorphic and strongly Ki-67 immunoreactive. The nodules were diagnosed as true sarcoma. To the best of our knowledge, this is 11th published case report of a PRMC with mural nodules.
机译:原发性腹膜后粘液性囊腺癌(PRMC)是一种极为罕见的病变。迄今为止,仅报告了49例。 PRMC中壁结节的存在可能表明预后较差。我们报道了一名40岁的日本妇女,患有PRMC并伴有壁瘤。显微镜检查发现结节的基质细胞呈纺锤形,大小不一。结节对波形蛋白具有免疫反应性,而对细胞角蛋白和EMA呈阴性,并且基质细胞核呈多形性,且具有强Ki-67免疫反应性。结节被诊断为真正的肉瘤。据我们所知,这是PRMC带有壁瘤的第11例病例报告。

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