首页> 外文期刊>Journal of the Siena Academy of Sciences >BILATERAL VESICO-URETERAL REFLUX IN PATIENT WITH CROSSED RENAL ECTOPIA AND FUSION TYPE A
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BILATERAL VESICO-URETERAL REFLUX IN PATIENT WITH CROSSED RENAL ECTOPIA AND FUSION TYPE A

机译:交叉性肾外膜异位和融合型A型患者的双侧输尿管反流

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Introduction. Crossed renal ectopia with fusion is a very rare congenital anomaly and the reported incidence varies between 1:1000 and 1:7000. The kidney is located on the opposite site of the mid- line from where the ureter enters the bladder. Eighty-five percent of crossed renal ectopia kid- neys are fused from below to the normally located kidney. This anomaly is more frequent for left kidney and it’s associated with vesico-ureteral re- flux (VUR) in 25-70% of cases. We report the management of a six-years-old patient with Pluri- malformative Syndrome, trisomy p16 and mono- somy q2, crossed renal ectopia with fusion type A and bilateral vesico-ureteral reflux (grade IV in the right kidney and grade III in the left).Materials and Methods. A 6-year-old boy was ammitted to our hospital for UTI in plurimalfor- mative syndrome characterized at birth by cleft palate, macrocephaly, congenital clubfeet, twisted right arm, congenital dysplasia of the hip, balanic hypospadias, bilateral inguinal hernia, right renal agenesis and epilepsy tonic-clonic. MRI revealed a fusion of the ectopic kidney with the left ortho- topic kidney (crossed renal ectopia with fusion type A). Voiding cystography showed a dilatated ureter of the crossed ectopic kidney passing across the midline and of the left ureter, and a bilateral vesico-ureteral reflux ( grade IV VUR in the right kidney and grade III VUR in the left). For this reason bilaterally endoscopic subureteral infiltra- tion was performed with Deflux ( 0.3 cc for side). Results. Patient was discharged in third day and he took antibiotic for one week. There weren’t complications like fever, obstruction or UTI. Fol- low-up after 1 month is normal and there weren’t UTI. Conclusion. Generally the outcome of patients with fused crossed renal ectopia is good. Presence of associated pathology likeVUR, could lead to a progressive deterioration of renal function. There- fore, in patient with uninhabited kidney area and UTI, it’s very important a carefull radiological in- vestigation to exclude a renal ectopy complicated by RVU and especially to realize an appropriate treatment strategy before the patient develops a chronic renal failure. Endoscopic infiltration with Deflux, in our case, was detected a viable surgical technique for its minimally invasiveness and also for its efficacy with a relatively short hospital stay.
机译:介绍。交叉肾外翻融合术是一种非常罕见的先天性异常,报道的发生率在1:1000和1:7000之间变化。肾脏位于输尿管进入膀胱的中线的相对位置。百分之八十五的交叉肾脏外翻肾脏从下方融合到正常位置的肾脏。这种异常在左肾中更为常见,在25-70%的病例中与膀胱输尿管返流(VUR)有关。我们报告了一名6岁的多形畸形综合征,p16三体性综合征和q2单体综合征,合并A型和双侧膀胱-输尿管反流的肾外翻患者的管理(右肾为IV级,而肾为III级)。左边)。材料和方法。一个6岁男孩因多形性综合征而入院我科,因为其特点是出生时出现macro裂,大头畸形,先天性马蹄内翻足,右臂扭曲,先天性髋关节发育不良,龟头尿道下裂,双侧腹股沟疝,右肾发育不全和癫痫强直阵挛。 MRI显示异位肾脏与左正位肾脏融合(交叉肾异种合并A型融合)。膀胱造影检查显示交叉异位肾脏的输尿管扩张,穿过中线和左输尿管,双侧膀胱输尿管反流(右肾为IV VUR,左为III VUR)。因此,双侧内镜下输尿管浸润是用Deflux(侧面0.3 cc)进行的。结果。患者在第三天出院,他服用了抗生素一周。没有发烧,阻塞或泌尿道感染等并发症。 1个月后随访是正常的,没有UTI。结论。通常,融合性交叉性肾外翻患者的预后良好。诸如VUR的相关病理可能会导致肾脏功能的逐步恶化。因此,对于无人居住的肾脏区域和UTI的患者,进行仔细的放射学检查以排除合并RVU的肾异位,尤其是在患者发展为慢性肾衰竭之前实现适当的治疗策略非常重要。在我们的案例中,内镜下用Deflux进行浸润被认为是一种可行的外科手术技术,因为它具有微创性,并且在相对短的住院时间内就具有疗效。

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