[MUCINOUS CYSTIC TUMOR OF LOW MALIGNANT POTENTIAL THOUGHT TO BE OF URACHAL ORIGIN: A CASE REPORT].

Atsuto Suzuki, Takeaki Noguchi, Noriaki Noto, Taku Mitome, Jun Kasuga, Futoshi Sano, Ichiro Ikeda
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Abstract

Mucinous cystic tumor of low malignant potential (MCTLMP) is a very rare disease.The patient was a 50-year-old man. Contrast-enhanced computed tomography and magnetic resonance imaging showed a multiocular cystic lesion on the top of the bladder. We performed surgery to remove the tumor for definitive diagnosis. Intraoperative rapid pathological diagnosis of the cyst wall showed no malignant findings, so we performed combined resection of the peritoneum and part of the bladder wall.Based on imaging findings, tumor location, and pathological and immunostaining findings (CK20 and CDX2 positivity; β-catenin negativity), the patient was diagnosed with MCTLMP thought to be of urachal origin. After the operation, recurrence was not observed.

[被认为是泌尿道起源的低恶性度粘液性囊肿:病例报告]。
低恶性潜能粘液性囊肿(MCTLMP)是一种非常罕见的疾病。对比增强计算机断层扫描和磁共振成像显示,膀胱顶部有一个多囊性病变。我们进行了手术切除肿瘤,以明确诊断。根据影像学结果、肿瘤位置、病理和免疫染色结果(CK20和CDX2阳性;β-catenin阴性),患者被诊断为泌尿系来源的MCTLMP。术后未见复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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