Niu Zhi Bin, Yang Yi, Hou Ying, Chen Hui, Wang Chang Lin
Shengjing Hospital of China Medical University, 36 Sanhao Road, Heping District, Shenyang, China.
Pediatr Surg Int. 2007 Apr;23(4):323-6. doi: 10.1007/s00383-007-1884-z. Epub 2007 Feb 15.
To better define the demographics, urothelial distribution and typical gross anatomic and radiologic appearances of fibroepithelial polyps of the ureter in children. We reviewed 15 cases of fibroepithelial polyps of the ureter with hydronephrosis from the archives of our department. Data were collected from radiographic studies, gross anatomic pathology and pathology and radiology reports and categorized by age, sex, clinical presentation, lesion size and location. The mean patient age was 9.1 years, and 80% were male. All of them presented with hematuria and/or flank pain. The polyps were located in the upper ureter or ureteropelvic junction (UPJ) and pelvis. Of the polyps, 60% were multiple polyps or filiform, and 40% were single or bilobed and 1-6 cm in size. Only four cases showed typical filling defect on intravenous urography. In five cases, sonography showed a mildly echogenic structure extending into the ureter from the renal pelvis. Enhanced CT revealed soft tissue filling UPJ or/and proximal ureter in six cases, and hydroureter was found in one case by three-dimensional (3D) image. Fibroepithelial polyps were diagnosed in all cases by postoperative histological examination. Fibroepithelial polyps are the most common benign tumors of the ureter. Congenital factor may be associated with the origin of fibroepithelial polyps in children. The preoperative diagnosis of ureteral polyps is difficult. A history of flank pain, hematuria or both, other than abdominal mass, light-to-moderate hydronephrosis with soft-tissue in UPJ or upper ureter, shown by sonography and radiological examination, may help in the diagnosis of ureteral polyps in children. Ureteral polyps should be recognized as an important etiology for hydronephrosis in children.
为了更明确儿童输尿管纤维上皮息肉的人口统计学特征、尿路上皮分布以及典型的大体解剖和放射学表现。我们回顾了本部门存档的15例伴有肾积水的输尿管纤维上皮息肉病例。数据收集自影像学研究、大体解剖病理学以及病理和放射学报告,并按年龄、性别、临床表现、病变大小和位置进行分类。患者的平均年龄为9.1岁,80%为男性。他们均表现为血尿和/或胁腹疼痛。息肉位于输尿管上段或输尿管肾盂连接处(UPJ)及肾盂。其中,60%的息肉为多发性或丝状,40%为单发性或双叶性,大小为1 - 6厘米。仅4例在静脉肾盂造影上显示典型的充盈缺损。5例超声检查显示有一轻度回声结构从肾盂延伸至输尿管。增强CT显示6例UPJ或/和输尿管近端有软组织充盈,三维(3D)图像显示1例有输尿管积水。所有病例均通过术后组织学检查确诊为纤维上皮息肉。纤维上皮息肉是输尿管最常见的良性肿瘤。先天性因素可能与儿童纤维上皮息肉的起源有关。输尿管息肉的术前诊断困难。胁腹疼痛、血尿或两者兼有,而非腹部肿块,超声和放射学检查显示UPJ或输尿管上段有轻至中度肾积水并伴有软组织,可能有助于儿童输尿管息肉的诊断。输尿管息肉应被视为儿童肾积水的一个重要病因。