Evidence map›Paper›PMID 39188620›Full record

ArticleRadiology case reports2024

Bilateral complete ureter duplication presenting with hydronephrosis and spontaneous stone passage in a 25-year-old male: A rare case report.

Yousef Alsaffaf, Aamer Razzouk, Hazem Arab, Mohammad Shehadeh

Abstract readCase Reports
In one paragraph

Article in Radiology case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Yousef AlsaffafFaculty of Medicine, Hama University, Hama, Syria.
Aamer RazzoukFaculty of Medicine, Hama University, Hama, Syria.
Hazem ArabFaculty of Medicine, Hama University, Hama, Syria.
Mohammad ShehadehDepartment of Urology, Hama National Hospital, Hama, Syria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ureteric duplication is a rare anomaly in the urinary tract, with an incidence of 0.5% to 3%. Bilateral double ureters are even rarer, occurring in 1 of 500 individuals. A 25-year-old man presented with right flank pain and nausea. Physical examination revealed tenderness at the right renal angle. Urinalysis demonstrated microscopic hematuria, and Ultrasound showed enlargement in the lower pole of the right kidney, while the upper pole appeared normal. Intravenous pyelography confirmed bilateral complete ureter duplication. However, after a week of observation, a 5 mm calcium oxalate stone was passed, and this event demonstrated the underlying cause of hydronephrosis in the lower pole of the right kidney. Bilateral complete ureter duplication is a rare anomaly in the urinary tract. To our knowledge, the presence of bilateral complete ureter duplication with a single stone in the right limb of the right double ureter is a unique case that has not been reported in the existing literature.

Indexed as

Bilateral complete ureteral duplicationCase reportHydronephrosisIntravenous pyelogramsUreteral stoneUreteric duplication

Identifiers

PMID39188620
PMCPMC11345281

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.