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Spontaneous combined rupture of a pelvicalyceal cyst into the collector system and retroperitoneal space during the acquisition of computed tomography scan images: a case report

机译:电脑断层扫描图像采集过程中骨盆腔囊肿自发合并破裂进入收集器系统和腹膜后腔的病例报告

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摘要

Abstract Introduction Pelvicalyceal cysts are common findings in autopsies and can manifest with a variety of patterns. These cystic lesions are usually a benign entity with no clinical significance unless they enlarge enough to cause compression of the adjacent collecting system and consequently obstructive uropathy. Few cases of the spontaneous rupture of pelvicalyceal renal cysts have been published and to the best of our knowledge there is no report of a combined rupture to collector system and retroperitoneal space documented during a multiphase computed tomography. Case presentation We report a case of a ‘real-time’ spontaneous rupture of a pelvicalyceal cyst into the collecting system with fistulization into the retroperitoneum. The patient was a 78-year-old Caucasian man with a previous history of renal stones and a large pelvicalyceal renal cyst who was admitted to our Emergency department with acute right flank pain. A multiphase computed tomography was performed and the pre-contrast images demonstrated a right pelvicalyceal renal cyst measuring 12.0 × 6.1cm in the lower pole causing moderate dilation of the upper right renal collection system. In addition, a partially obstructive stone on the left distal ureter with mild left hydronephrosis was noted. The nephrographic phase did not add any new information. The excretory phase (10-minute delay) demonstrated a spontaneous rupture of the cyst into the pelvicalyceal system with posterior fistulization into the retroperitoneal space. Conclusion In this case study we present time-related changes of a rare pelvicalyceal cyst complication, which to the best of our knowledge has fortunately not been previously documented. Analysis of the sequential images and comparison with an earlier scan allowed us to better understand the physiopathological process of the rupture, the clinical presentation and to elaborate hypotheses for its etiopathogenesis.
机译:摘要简介睑板膜囊肿是尸体解剖中的常见发现,并且可以多种形式表现出来。这些囊性病变通常是无临床意义的良性实体,除非它们扩大到足以引起相邻收集系统受压并因此阻塞性尿路病的程度。据报道,极少发生骨盆腔肾囊肿自发性破裂的病例,据我们所知,尚无多阶段计算机断层扫描记录到收集器系统和腹膜后间隙合并破裂的报道。病例介绍我们报告一例“实时”自发性骨盆腔囊肿破裂进入收集系统,并有瘘管进入腹膜后。该患者是一名78岁的白人,曾有肾结石病史和较大的盆腔肾囊肿,因急性右胁腹痛入我们急诊科。进行了多阶段计算机体层摄影术,造影前图像显示右下颌骨中的右骨盆腔肾囊肿长12.0×6.1cm,导致右上肾收集系统适度扩张。另外,在左远端输尿管上发现了部分阻塞性结石,伴有轻度左肾积水。肾病相未添加任何新信息。排泄期(延迟10分钟)显示,囊肿自发性破裂进入骨盆腔系统,后瘘管进入腹膜后间隙。结论在本案例研究中,我们介绍了罕见的盆腔囊肿并发症的与时间相关的变化,据我们所知,幸运的是,以前没有文献记载。对顺序图像进行分析并与早期扫描进行比较,使我们可以更好地了解破裂的生理病理过程,临床表现,并详细阐述其病因。

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