Evidence map›Paper›PMID 39720324›Full record

ArticleEuropean journal of pediatric surgery reports2024

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

Theresa S Haecker, Thomas F Krebs, Regula von Allmen, Frank-Martin Haecker

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In one paragraph

Article in European journal of pediatric surgery reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Theresa S HaeckerDepartment of Pediatric Surgery, Children's Hospital of Eastern Switzerland, St. Gallen, Switzerland.
Thomas F KrebsDepartment of Pediatric Surgery, Children's Hospital of Eastern Switzerland, St. Gallen, Switzerland.
Regula von AllmenDepartment of Vascular Surgery, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Frank-Martin HaeckerDepartment of Pediatric Surgery, Children's Hospital of Eastern Switzerland, St. Gallen, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

adolescentsarterio–ureteral fistulachronic indwelling ureteral stenthematuriapelvic surgery

Identifiers

PMID39720324
PMCPMC11668556

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