Haecker Theresa S, Krebs Thomas F, Allmen Regula von, Haecker Frank-Martin
Department of Pediatric Surgery, Children's Hospital of Eastern Switzerland, St. Gallen, Switzerland.
Department of General, Visceral, Thoracic, Transplant and Pediatric Surgery, University Hospital of Schleswig-Holstein Kiel Campus, Kiel, Germany.
European J Pediatr Surg Rep. 2024 Dec 24;12(1):e95-e98. doi: 10.1055/a-2496-5087. eCollection 2024 Jan.
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.
动脉输尿管瘘(AUF)是一种罕见疾病,仅影响成年患者。患者通常表现为血尿,起初常为间歇性血尿,随后频繁加重,甚至可能导致失血性休克。若未得到快速诊断和及时治疗,AUF可能致命。AUF的危险因素包括主要因癌症进行的盆腔手术史、盆腔放疗史、血管手术史或慢性输尿管支架置入史(CIUS)。用于确诊的影像学检查包括血管造影、计算机断层扫描(CT)或逆行肾盂造影,不过AUF可能漏诊。因此,即便影像学检查结果为阴性,但不明原因血尿伴有上述危险因素时,AUF高度可疑,必须排除。我们报告一例16岁男性患者,其因新发间歇性血尿就诊于我院急诊室。患者既往史包括6年前因神经节细胞瘤行盆腔手术,术中双侧髂动脉置换,术后出现急性肾衰竭,双侧输尿管重建并置入CIUS。术后最初5年随访无异常,之后因肾积水在右侧输尿管置入另一根双J(DJ)导管。六周后,患者出现间歇性血尿。尽管影像学检查阴性,我们仍立即进行手术探查,确诊为AUF。据我们所知,这是文献报道的首例18岁以下AUF病例。总之,对于有肉眼血尿且存在上述危险因素的患者,必须考虑AUF并可靠排除。