首页> 外文期刊>Journal of the Siena Academy of Sciences >RENAL DUPLEX SYSTEM IN PEDIATRIC POPULATION: MANAGEMENT AND LONG-TERM FOLLOW-UP
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RENAL DUPLEX SYSTEM IN PEDIATRIC POPULATION: MANAGEMENT AND LONG-TERM FOLLOW-UP

机译:小儿人口肾脏双重系统:管理和长期随访

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Duplex system is a duplication of renal parenchyma, pelvis and collecting system. It could be complete, if ureters lead to bladder separately or incomplete, if they joint before coming out. This study aims duplex system management evaluation, defining indications of conservative or demolitive therapy, and results. Materials and methods. At the section of pediatric surgery of University of Siena we have observed 27 patients with duplex system from January 1980 to May 2011: 7 male (26%) and 20 female (74%), 18 (67%) with complete duplicity, 9 (33%) with incomplete one. Patients were divided into 2 groups: the first one was composed by 12 children (44%), they had negative diagnostic exams for alterations of renal function and associated diseases and no symptoms;the second group had 15 children (56%) whose diagnostic-therapeutic iter was based on associated malformations and symptoms of each case. We found: 5 RVU (33%) with 1 Hutch diverticulum; 5 ureteroceles (33%); 3 ectopic ureters (20%); 4 megaureters (26%), 6 renal dysplasia and upper pole function <10% (40%). Results. Children belonging to second group were treated in different ways. 5 babies (33%) with RVU were approached with submeatal infiltration; 1 baby (7%) with ureterocele was treated with excision of the malformation and Cohen reimplatation; 2 ureteroceles (13%) were incised by transurethral approach and RVU appeared, 1 of them was then treated with eminephroureterectomy; in 1 case of ureterocele (7%)and 1 of ectopic ureter (7%) no treatment was undertaken and 1 baby with ureterocele (7%) needed eminephoureterectomy; 4 kidneys (26%) with upper pole impaired function required em- inephroureterectomy. All second group patients, except 3, had a 2-16 years follow-up and they showed normal growth and no symptoms. First group children had negative exams and excellent clinic conditions. Conclusions. Our results suggest that management should be decided on patient’s age, clinic presentation and associated diseases.
机译:双工系统是肾实质,骨盆和收集系统的重复。如果输尿管分别引至膀胱,则可能是完整的;如果输尿管在流出前已接合,则可能不完整。这项研究旨在评估双系统的管理评估,定义保守或拆除疗法的适应症和结果。材料和方法。在锡耶纳大学的儿科外科部分,我们观察了1980年1月至2011年5月的27例双系统患者:男性7例(26%)和女性20例(74%),18例(67%)完全重复,9例( 33%),其中一项不完整。患者分为两组:第一组由12名儿童组成(44%),他们对肾功能和相关疾病的改变进行了阴性诊断检查,没有症状;第二组有15名儿童(56%)的诊断-根据每个病例的相关畸形和症状进行治疗。我们发现:5 RVU(33%)与1 Hutch憩室; 5个输尿管囊肿(33%); 3个异位输尿管(20%); 4个大输尿管(26%),6个肾发育不良和上极功能<10%(40%)。结果。属于第二组的儿童受到了不同的对待。对5名RVU婴儿(33%)进行了肉下浸润;切除畸形并再行Cohen再植入治疗输尿管膨出1例(7%)。经尿道切开2例输尿管囊肿(13%),出现RVU,其中1例接受了肾盂肾切除术治疗; 1例输尿管囊肿(7%)和1例异位输尿管囊肿(7%)未接受治疗,1例输尿管囊肿婴儿(7%)需要行红细胞输尿管切除术。需要进行上肾电镜切除术的4个肾脏(26%)具有上极功能受损。除3例外,所有第二组患者均进行了2-16年的随访,并显示出正常的生长且无症状。第一组儿童的检查阴性,并且临床状况良好。结论。我们的结果表明,应根据患者的年龄,临床表现和相关疾病决定治疗方案。

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