Arterio-Ureteral Fistula as a Long-term Complication Following Retroperitoneal Presacral Ganglioneuroma Resection: Case Report in an Adolescent and Review of the Literature.

IF 0.6 Q4 SURGERY European Journal of Pediatric Surgery Reports Pub Date : 2024-12-24 eCollection Date: 2024-01-01 DOI:10.1055/a-2496-5087
Theresa S Haecker, Thomas F Krebs, Regula von Allmen, Frank-Martin Haecker
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Abstract

Arterio-ureteral fistula (AUF) is a rare condition affecting nearby adult-only patients. Patients usually present with hematuria, often starting as intermittent hematuria which frequently increases, and may lead to hemorrhagic shock. Without rapid diagnosis and prompt treatment, AUF can be lethal. Risk factors for developing an AUF include a history of pelvic surgery mainly due to cancer, a history of pelvic radiation, a history of vascular surgery, or chronic indwelling ureteral stents (CIUS). Imaging to confirm diagnosis includes angiography, computed tomography (CT) scan, or retrograde pyelography, although AUF may be missed. Therefore, even if imaging is negative, the presence of hematuria of unexplained origin in combination with mentioned risk factors is highly suspicious for AUF and must be excluded. We report the case of a 16-year-old male patient who presented with a new onset of intermittent hematuria to our emergency room. The patient's history included previous pelvic surgery for resection of ganglioneuroma 6 years ago with bilateral replacement of the iliac artery and postoperative acute kidney failure with reconstruction of both ureters and CIUS. After the initial uneventful postoperative follow-up over 5 years, another Double J (DJ) catheter had to be placed into the right ureter due to hydronephrosis. Six weeks later, the patient presented with intermittent hematuria. Despite negative imaging, we performed immediate surgical exploration confirming the diagnosis of AUF. To the best of our knowledge, this is the first case of AUF under the age of 18 years reported in the literature. In conclusion, in patients with macrohematuria and a history of the abovementioned risk factors, AUF has to be kept in mind and must be reliably excluded.

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动脉输尿管瘘作为腹膜后骶前神经节神经瘤切除术后的长期并发症:一例青少年病例报告及文献回顾。
动脉输尿管瘘(AUF)是一种罕见的疾病,仅影响附近的成人患者。患者通常表现为血尿,常以间歇性血尿开始,频繁加重,并可导致失血性休克。如果没有快速诊断和及时治疗,AUF可能是致命的。发生AUF的危险因素包括主要由癌症引起的盆腔手术史、盆腔放疗史、血管手术史或慢性留置输尿管支架(CIUS)。确诊的影像学包括血管造影、计算机断层扫描(CT)或逆行肾盂造影,尽管AUF可能会被遗漏。因此,即使影像为阴性,原因不明的血尿合并上述危险因素也高度怀疑是AUF,必须排除。我们报告的情况下,一个16岁的男性患者谁提出了一个新的发作间歇性血尿到我们的急诊室。患者病史包括6年前盆腔手术切除神经节神经瘤伴双侧髂动脉置换术,术后急性肾衰竭伴输尿管和CIUS重建。术后5年多的随访后,由于肾积水,再次将双J (DJ)导管置入右输尿管。6周后,患者出现间歇性血尿。尽管呈阴性,我们还是立即进行了手术探查,确认了AUF的诊断。据我们所知,这是文献中报道的第一例未满18岁的AUF。总之,对于有大量血尿且有上述危险因素病史的患者,必须牢记并可靠地排除AUF。
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12 weeks
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Arterio-Ureteral Fistula as a Long-term Complication Following Retroperitoneal Presacral Ganglioneuroma Resection: Case Report in an Adolescent and Review of the Literature. Anal Sphincter Reconstruction Using the Posterior Sagittal Approach for Pediatric Perineal Trauma. Enigma of Gastric Teratoma in Infants: A Case Series. Transverse Testicular Ectopy and an Incarcerated Inguinal Hernia in a 2-Month-Old Preterm Boy. Pulmonary Inflammatory Myofibroblastic Tumor: A Case Report.
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