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首页> 外文期刊>The Internet Journal of Urology >Intra-renal Pseudo-aneurysm as a complication of DJS insertion: case report & literature review
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Intra-renal Pseudo-aneurysm as a complication of DJS insertion: case report & literature review

机译:肾内假性动脉瘤作为DJS插入的并发症:病例报告及文献复习

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Ureteric double J stenting is one of the important urologic procedures which is not free of complications. We report a case of a 55-year- old male patient who presented with macroscopic hematuria after DJS insertion. Angiography confirmed the presence of an intra-renal pseudo-aneurysm . Selective arterial embolization was performed successfully. Because of the rarity of the case, we decided to report it and review the literature on the subject Introduction Renal artery aneurysms constitute 22% of all visceral aneurysms, and their prevalence in the population varies from 0.01% to 1.0% [6]. Intrarenal aneurysms constitute 17% of all renal artery aneurysms [7];The incidence of iatrogenic renovascular lesions has increased significantly, with the increase in the performance of minimally invasive urological procedures.[14] Intra renal pseudo-aneurysms are more commonly described as a complication of percutaneous procedures[15,16],and there are few reports of this complication following endourological surgeries[17] .The objective of this paper is to report an intra-renal pseudo-aneurysm following DJS insertion. To our knowledge, there is no documented report for such a case. Case Report A 55year old male patient , known ischemic heart disease ,diabetic, hypertensive & hypercholesterimic ,had a history of ureteric injury ,at the junction between the middle & the lower third , secondary to a complicated left ureteroscopy & laser stone fragmentation . That was managed by DJS insertion. Six weeks latter, the patient underwent removal of the DJS & retrograde pyelography which showed stricture at the lower third of the ureter, at the crossing of the iliac vessels, corresponding to the previous area of perforation. A Guide wire was introduced ,then ureteroscopy was performed which confirmed the stricture . Balloon dilatation was then done. Over the guide wire , ureteric dilatation using the balloon Ureteral dilator size 7F (4cm length balloon ) was done under fluoroscopy guidance. 1.5 ml of dye was used to inflate the balloon .The balloon was kept inflated for 3 minutes.During dilatation , the balloon ruptured & fluoroscopy showed dye leaking ,at the stricture area, into the retroperitoneal space surrounding the left iliac vessels course signifying ureteric perforation.Intra operatively , the patient was vitally stable & no bleeding could be identified. Next, the balloon was withdrawn & size 6F DJS was inserted smoothly over the guide wire to bridge the site of perforation. Post operatively, the patient was vitally stable with minimal hematuria.At the second day post operative, the patient developed acute coronary syndrome with chest pain . Cardiac enzymes & ECG where all with in normal. .He was managed by Tridil (Nitroglycerin) infusion (from 10meq/min tapered to 2meq/min till discontinued)& Isordil (Isosorbide dinitrate) 5mg sublingually TID for 5days after which the patient was discharged in a good general condition, stable vitals, clear urine & hemoglobin of 12g/dl. Five days latter , the patient presented to the Emergency department with frank hematuria with clots. There was no history of direct kidney trauma nor dysuria. The patient was conscious, oriented with Bp 150/80, pulse 105 .Abdominal examination was within normal. His lab investigations : CBC: wbcs 9.95 , Hb 7.6 , Plt 424, Coagulation profile was normal.Creatinine 126 The patient was admitted to the surgical ward. Intravenous fluids were started & Foley's catheter (3 way with irrigation) was inserted. Two units of PRBCs were transfused , Fortum (Ceftazidime) 1gram I.V Q12 h was started .Because of the recent ureteric perforation near the crossing of the iliac vessels, the patient was presumed to have uretero- iliac fistula C.T angio was done which showed left perinephric collection. The crossing point of the left ureter over the left iliac vessels , with DJS at normal position and the iliac vessels were clearly visualized. This ruled out uretero- iliac fistula.( Figure 1).Th
机译:输尿管双J支架置入术是重要的泌尿外科手术之一,它没有并发症。我们报告了一例55岁的男性患者,在DJS插入后出现肉眼血尿。血管造影证实存在肾内假性动脉瘤。选择性动脉栓塞术成功进行。由于该病例的罕见性,我们决定对其进行报告并复习有关该主题的文献。引言肾动脉瘤占所有内脏动脉瘤的22%,其在人群中的患病率从0.01%到1.0%不等[6]。肾内动脉瘤占全部肾动脉瘤的17%[7];随着微创泌尿外科手术的执行,医源性肾血管病变的发生率显着增加。[14]肾内假性动脉瘤被更普遍地描述为经皮手术的并发症[15,16],而在泌尿外科手术后很少有这种并发症的报道[17]。本文的目的是报告肾内假性动脉瘤。 DJS插入后的动脉瘤。据我们所知,没有关于这种情况的书面报告。病例报告一名55岁的男性患者,已知为缺血性心脏病,糖尿病,高血压和高胆固醇血症,有输尿管损伤史,位于中下部三分之一之间的交界处,继发于复杂的左输尿管镜检查和激光结石碎裂。这是通过DJS插入来管理的。六周后,患者接受了DJS和逆行肾盂造影术,这表明输尿管下部三分之一处,the骨血管交叉处出现狭窄,与先前的穿孔区域相对应。引入导丝,然后进行输尿管镜检查以确认狭窄。然后进行球囊扩张。在导丝上,使用球囊进行扩张术,在荧光检查指导下使用尺寸为7F(长度为4cm的球囊)的输尿管扩张器进行输尿管扩张。用1.5 ml的染料给球囊充气。将球囊充气3分钟。在扩张过程中,球囊破裂并通过荧光检查显示,在狭窄区域,染料渗漏到了左血管周围的腹膜后间隙,这表明输尿管穿孔。术中,患者生命稳定,未发现出血。接下来,取出球囊,将6F DJS尺寸平稳地插入导丝上方,以桥接穿孔部位。术后,患者生命稳定,血尿极少。术后第二天,患者发展为伴有胸痛的急性冠脉综合征。心脏酶和心电图均正常。用Tridil(硝酸甘油)输注(从10meq / min逐渐减少到2meq / min直至停药)和Isordil(硝酸异山梨酯)舌下TID 5mg治疗5天,此后患者一般情况良好,生命力稳定,清澈尿和血红蛋白为12g / dl。五天后,患者因血凝块而出现坦率血尿。没有直接的肾脏创伤或排尿困难的病史。患者有意识,以Bp 150/80,脉冲105定向。腹部检查在正常范围内。他的实验室检查:CBC:wbcs 9.95,Hb 7.6,Plt 424,凝血曲线正常。肌酐126病人被送往外科病房。开始静脉输液,并插入Foley导管(3冲洗方式)。输注两个PRBCs,开始Fortum(Ceftazidime)1克IV Q12 h。由于近期在血管交叉处附近出现输尿管穿孔,因此该患者被认为患有输尿管瘘。采集。左输尿管在左血管上的交叉点,DJS处于正常位置,clearly血管清晰可见。这排除了输尿管瘘(图1)。

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