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Primary Retroperitoneal Mucinous Cystadenocarcinoma: A Case Report and Review of the Literature

机译:原发性腹膜后黏液性膀胱腺癌:一例报道并文献复习

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摘要

Primary retroperitoneal mucinous cystadenocarcinoma is a rare tumor. Only about 30 such cases have been reported in the worldwide literature, and a few Korean cases have been reported. The pathogenesis is not clear, and coelomic metaplasia of the retroperitoneal mesothelium has gained wide support. There is no consensus on the appropriate treatment, but surgical exploration is needed for the diagnosis and treatment, and adjuvant chemotherapy may be recommended following complete surgical excision. The long-term prognosis has not been established.We report here on a 32-year-old woman who was diagnosed as having a retroperitoneal mucinous cystadenocarcinoma with mural nodules of sarcomatoid change. Tumor excision and adjuvant chemotherapy were done and the patient is doing well without any evidence of recurrence at 42 months postoperatively.
机译:原发性腹膜后粘液性囊腺癌是一种罕见的肿瘤。全球文献中仅报道了约30个此类病例,而韩国也报道了一些病例。发病机制尚不清楚,腹膜后间皮的结肠化生已获得广泛支持。对于合适的治疗方法尚无共识,但诊断和治疗仍需进行外科手术探索,并建议在完全手术切除后进行辅助化疗。长期预后尚未确定。我们在这里报道了一名32岁的妇女,她被诊断患有腹膜后粘液性囊腺癌,并伴有肉瘤样改变的壁结节。进行了肿瘤切除和辅助化学疗法,并且患者在术后42个月无任何复发迹象,情况良好。

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