999精品在线视频,手机成人午夜在线视频,久久不卡国产精品无码,中日无码在线观看,成人av手机在线观看,日韩精品亚洲一区中文字幕,亚洲av无码人妻,四虎国产在线观看 ?

Spontaneous distal ureteric rupture: A rare case report and review of literature

2020-03-21 16:19:54LiSianLowShivaMadhwanNair
Asian Journal of Urology 2020年1期

Li Sian Low*, Shiva Madhwan Nair

Urology Department, Waikato Hospital, Hamilton, Waikato, New Zealand

Abstract Spontaneous rupture of the ureter is a very interesting and unusual phenomenon which normally occurs due to ureteral obstruction. We present a case of spontaneous rupture of the distal ureter, secondary to a ureteric calculus. Our patient presented with a history of acute on chronic abdominal pain and was septic on arrival to hospital.

KEYWORDS Spontaneous;Distal ureteric calculi;Ureteric rupture

1. Introduction

Spontaneous ureteric rupture is an extremely rare condition in which there is evidence of urine extravasation from the ureter. Published cases have reported pregnancy, ureteral strictures, tumours, bladder outlet obstruction and retroperitoneal fibrosis among the contributing causes [1].Majority of reported incidents generally involve the proximal ureter, renal fornix or pelviureteric junction [2]. Only hypothetical causes have been suggested and thus, there are no recommended guidelines to aid management. Management principles are based on the current condition of the patient including diversion of urine, management of sepsis, followed by definitive treatment. Placements of double-J stents or percutaneous nephrostomy for drainage provides excellent results in the unwell patient, until definitive surgery can be performed. Conservative management with antibiotics is recommended. Improved nutritional status of the patient is imperative for postoperative recovery. We describe the first reported case of spontaneous distal ureteric rupture,secondary to a ureteric calculus.

2. Case report

A 48-year-old female presented to the Emergency Department with left lower quadrant abdominal pain. Her symptoms have been gradually increasing in intensity over the last few months. Apart from a previous diagnosis (5 years ago)of a 4 cm benign uterine fibroid on ultrasound,she had no significant medical history.Examination of her abdomen revealed localised tenderness at the left lower quadrant with a palpable mass. Laboratory evaluation showed evidence of leukocytosis (white blood cell count [WBC]15.99×109/L) with neutrophilia (12.87×109/L). Her Creactive protein (CRP) was raised at 300 mg/L, with total albumin of 19 g/L. Urine microscopy and renal function were unremarkable. An ultrasound was obtained immediately, which showed a large adnexal mass measuring 9.5 cm×7.9 cm×7.9 cm with cystic and solid components.Left sided moderate hydronephrosis was evident as well.She was placed on antibiotics and an urgent magnetic resonance imaging (MRI) scheduled.

MRI showed a large multiloculated cystic collection with evidence of a calculus 1.5 cm×1.3 cm below it (Fig. 1). A large urinoma was also seen surrounding the ureter while the left kidney showed marked loss of parenchyma and severe hydronephrosis.A pigtail drain was also inserted into the cystic collection, followed by insertion of a percutaneous nephrostomy.Frank pus was aspirated from the renal pelvis, which cultured Streptococcus anginosus. Culture from the collection grew Streptococcus anginosus and Peptoniphilusas accharolyticus. A computed tomography(CT) scan was obtained 2 days following the MRI (Fig. 2).

A nephrostogram was performed 2 days later, which revealed contrast leaking from the distal ureter into the large cystic space (Fig. 3). No contrast was seen draining into the bladder. A follow-up CT scan after 3 days showed resolution of the left hydroureteronephrosis and decrease in the size of pelvic collection. Her WBC and CRP improved with antibiotic treatment.

Following that, a dimercaptosuccinic acid (DMSA) renogram demonstrated that the left kidney had approximately 9.5% differential function. Options of treatment were discussed with the patient including longer term nephrostomy or delayed nephrectomy. Rationale for delayed nephrectomy was to allow resolution of chronic sepsis and improvement in physiological status of the patient.She was discharged on oral antibiotics, nutrition supplements, free draining nephrostomy tube and an open left nephrectomy planned. Her CRP and total albumin improved to 21 mg/L and 25 g/L respectively on discharge.

Figure 1 High resolution sagittal T2 weighted magnetic resonance imaging showing the urinoma(star)and the ureteric wall disruption (white arrow). The stone (black arrow) and bladder with an in dwelling urinary catheter (red arrow) are highlighted.

Figure 2 Delayed contrast enhanced computed tomography 2 days following the magnetic resonance imaging showing the posterior displacement of the stone (black arrow) and the urinoma (star). The site of the rupture is highlighted (white arrow).

Figure 3 Nephrostogram obtained 3 days following percutaneous nephrostomy tube (arrow) insertion and drainage of pelvic/retroperitoneal collection, showing ureteric disruption with extravasation of contrast (star).

The procedure was performed electively once her overall condition improved. Intraoperatively, the simple nephrectomy had similar features to a nephrectomy performed for xanthogranulomatous pyelonephritis. Due to this intraoperative finding,we opted not to pursue her distal ureteric stone (which was in her pelvis) minimizing morbidity from the procedure. Her post-operative course was uncomplicated,and she made excellent recovery.She was discharged on day 3 post surgery, with no further antibiotics. She was given advice on stone prevention and a plan for early intervention if she has recurrence of stone disease. We intend to explore her pelvis and remove the extramural ureteric stone, should she develop a recurrence of a pelvic abscess? Sections of the nephrectomy specimen showed features in keeping with chronic pyelonephritis. Renal parenchyma shows distortion of architecture by interstitial scarring and chronic inflammatory infiltrates. Foci of xanthogranulomatous inflammation were also noted.

3. Discussion

Spontaneous ureteric rupture is a rarely described medical event which is challenging to diagnose. Urinoma or abscess formation may ensue, eventually leading to sepsis and death. Hale et al. [3] reported a case of mid-ureteral rupture secondary to traumatic urethral catheterization.The definition of “spontaneous” has not been properly established but our patient has never had previous ureteric instrumentation, kidney/abdominal surgery or a history of external trauma. However, the presence of obstructive pyonephrosis could also be secondary to a ureteral lesion,which may eventually lead to ureteric rupture and extravasation of pus.

Due its rarity, there are no recommended guidelines to direct management. Successful methods have been described which include retrograde insertion of a double-J ureteric stent and/or nephrostomy tube drainage both with the concurrent use of antibiotics [2,4]. These conduits normally remainin situ, until definitive surgery can be performed. For cases with no known causes, conduits are removed once patients’ clinical state improves with imaging consistent with resolution [5]. In general, prompt intervention will reduce both mortality and morbidity.Nevertheless, the general principles of controlling sepsis take precedence prior to definitive surgery.

In our patient, we elected for initial conservative management which included insertion of both percutaneous nephrostomy tube and a pig tail drain into the collection,along with an extended course of antibiotics.Subsequently,an antegrade study via the nephrostomy tube was performed to characterize and pinpoint the rupture. Finally,definitive treatment with nephrectomy was chosen due to the minimally functioning obstructed kidney, which would have predisposed her to urosepsis.

Author contributions

Study design: Li Sian Low, Shiva Madhwan Nair.

Data acquisition and analysis: Li Sian Low.

Drafting of manuscript: Li Sian Low.

Critical revision of the manuscript: Shiva Madhwan Nair.

Conflicts of interest

The authors declare no conflict of interest.

Acknowledgements

We would like to acknowledge Dr. Laxmi Lanka, Uroradiologist of Waikato Hospital for his help with supplementing the radiological images.

主站蜘蛛池模板: 人禽伦免费交视频网页播放| 亚洲精品午夜天堂网页| 国产三区二区| 波多野结衣亚洲一区| 亚洲黄色片免费看| 一区二区三区国产| 国产女主播一区| 日本午夜三级| 精品国产成人三级在线观看| 亚洲成人在线免费观看| 欧美黑人欧美精品刺激| 激情亚洲天堂| 国产成人三级| 色首页AV在线| 国产精品成人啪精品视频| 熟妇丰满人妻av无码区| 国产素人在线| 日韩无码视频专区| 精品国产91爱| 特级精品毛片免费观看| 综合天天色| 91久久国产综合精品女同我| 色婷婷在线播放| 亚洲人成网站日本片| 久草网视频在线| 欧美高清国产| 91精品专区| 欧美一道本| 精品夜恋影院亚洲欧洲| 老司机久久精品视频| 亚洲九九视频| 日韩经典精品无码一区二区| 亚洲欧美一区二区三区图片 | 精品日韩亚洲欧美高清a| 午夜精品一区二区蜜桃| 91激情视频| 欧美高清视频一区二区三区| 91无码网站| 国产成人精彩在线视频50| 精品无码人妻一区二区| 国产精品专区第1页| 国产精品成人一区二区| 99热这里都是国产精品| 日韩黄色在线| 97精品久久久大香线焦| 欧美a在线| 婷婷亚洲最大| 国产成人综合亚洲网址| 国产精品无码一区二区桃花视频| 55夜色66夜色国产精品视频| 99久久精品免费看国产免费软件 | 91在线一9|永久视频在线| 精品91在线| 亚洲av中文无码乱人伦在线r| 国产第八页| 四虎影视永久在线精品| 中文无码精品A∨在线观看不卡| 好吊妞欧美视频免费| 91小视频在线观看| 91福利一区二区三区| 亚洲欧美一区二区三区图片| 国产精品一区二区久久精品无码| 国产香蕉在线| 无码专区国产精品一区| 夜夜爽免费视频| 国产国拍精品视频免费看 | 人人爱天天做夜夜爽| 97久久超碰极品视觉盛宴| 久久亚洲综合伊人| 无码不卡的中文字幕视频| 亚洲成综合人影院在院播放| 在线观看视频一区二区| 久久特级毛片| 亚洲精品无码久久毛片波多野吉| 欧美午夜网| 夜夜操国产| 亚洲性视频网站| 国产一级无码不卡视频| 91久久天天躁狠狠躁夜夜| 亚洲综合经典在线一区二区| 欧美三级视频网站| 日韩美毛片|