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病例报告:小儿整块肾移植术后出现尿肠瘘,表现为隐匿性水样腹泻和正常阴离子间隙酸中毒。

Case Report: Uroenteric Fistula in a Pediatric-en-bloc Kidney Transplant Manifests as Deceptive Watery Diarrhea and Normal Anion Gap Acidosis.

作者信息

Al Barbandi Malek, Defreitas Marissa J, Infante Juan C, Morsi Mahmoud, Arroyo Parejo Drayer Patricia A, Katsoufis Chryso P, Seeherunvong Wacharee, Chandar Jayanthi, Burke George W, Abitbol Carolyn L

机构信息

Division of Pediatric Nephrology, Department of Pediatrics, University of Miami/Holtz Children's Hospital, Miami, FL, United States.

Division of Kidney/Pancreas Transplant, Department of Surgery, Miami Transplant Institute, University of Miami/Jackson Memorial Hospital, Miami, FL, United States.

出版信息

Front Pediatr. 2021 Jul 12;9:687396. doi: 10.3389/fped.2021.687396. eCollection 2021.

Abstract

The diagnosis of a post-surgical uroenteric fistula can be challenging and may be delayed for months after symptoms begin. A normal anion gap metabolic acidosis has been reported in up to 100% of patients after ureterosigmoidostomy, and bladder substitution using small bowel and/or colonic segments. Here, we describe a rare case of a pediatric patient who developed a uroenteric fistula from the transplant ureters into the small bowel, after an en-bloc kidney transplantation resulting in profound acidosis and deceptive watery diarrhea. The patient is an 8-year-old girl with end stage kidney disease (ESKD) secondary to focal segmental glomerulosclerosis. Through a right retroperitoneal approach, she underwent a right native nephrectomy and a pediatric deceased donor en-bloc kidney transplant including two separate ureters. One month later, she had a renal allograft biopsy for suspected rejection. During the week after the biopsy, she experienced abdominal pain followed by watery diarrhea and metabolic acidosis requiring continuous bicarbonate/acetate infusions. An extensive gastro-intestinal evaluation for the cause of the diarrhea including endoscopy was inconclusive. The urine output decreased to <500 ml daily; although, the kidney function remained normal. After 2 weeks of unexplained watery diarrhea a magnetic resonance urogram with contrast was performed which demonstrated extravasation of urine from both ureters with fistulization into the small bowel. She underwent corrective surgery which identified the fistulous tract, which was resected and both ureters were re-implanted. The diarrhea and acidosis resolved, and she has maintained normal renal allograft function for over 1 year. An important aspect in the early diagnosis of a uroenteric fistula is the sudden onset of severe hyperchloremic metabolic acidosis that results when urine is diverted into the intestinal tract. The mechanism is similar to that described in cases of urinary diversions and/or bladder augmentation using the intestine. Important diagnostic tools are the measurements of solute excretion and pH in the urine as compared to the "watery diarrhea" or bowel output. We describe a case of a uroenteric fistula in a pediatric-en-bloc kidney transplant patient that went undiagnosed for almost 3 weeks due to the deceptive nature of the watery diarrhea which was actually urine. A uroenteric fistula should be considered in the differential diagnosis of diarrhea and hyperchloremic metabolic acidosis as a complication of kidney transplant. The simultaneous comparison of stool and urine pH and solute excretions may lead to the diagnosis, appropriate imaging and surgical intervention.

摘要

术后尿肠瘘的诊断具有挑战性,症状出现后可能会延迟数月才得以确诊。据报道,在输尿管乙状结肠吻合术以及使用小肠和/或结肠段进行膀胱替代术后,高达100%的患者会出现正常阴离子间隙代谢性酸中毒。在此,我们描述了一例罕见的儿科患者,在整块肾移植后,移植输尿管与小肠之间形成了尿肠瘘,导致严重酸中毒和具有欺骗性的水样腹泻。该患者是一名8岁女孩,患有继发于局灶节段性肾小球硬化的终末期肾病(ESKD)。通过右腹膜后入路,她接受了右肾切除术和儿科脑死亡供体整块肾移植,移植肾包括两条独立的输尿管。一个月后,因怀疑排斥反应,她接受了移植肾活检。活检后的一周内,她出现腹痛,随后是水样腹泻和代谢性酸中毒,需要持续输注碳酸氢盐/醋酸盐。针对腹泻原因进行的包括内镜检查在内的广泛胃肠道评估未得出明确结论。尿量降至每日<500 ml;不过,肾功能仍保持正常。在出现无法解释的水样腹泻2周后,进行了增强磁共振尿路造影,结果显示双侧输尿管尿液外渗并形成瘘管进入小肠。她接受了矫正手术,术中发现了瘘管并将其切除,两条输尿管均重新植入。腹泻和酸中毒得到缓解,她的移植肾功能维持正常已超过1年。尿肠瘘早期诊断的一个重要方面是当尿液改道进入肠道时突然出现的严重高氯性代谢性酸中毒。其机制与使用肠道进行尿流改道和/或膀胱扩大术的病例中所描述的机制相似。重要的诊断工具是将尿液中的溶质排泄量和pH值与“水样腹泻”或肠道排泄物进行比较测量。我们描述了一例儿科整块肾移植患者的尿肠瘘病例,由于水样腹泻具有欺骗性(实际上是尿液),该病例几乎3周未被诊断出来。在鉴别诊断作为肾移植并发症的腹泻和高氯性代谢性酸中毒时,应考虑尿肠瘘。同时比较粪便和尿液的pH值及溶质排泄量可能有助于诊断、进行适当的影像学检查和手术干预。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95e5/8310905/a7a8fa01a4c0/fped-09-687396-g0001.jpg

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