Evidence map›Paper›PMID 36915294›Full record

ArticleCase reports in women's health2023

Congenital uterine arteriovenous malformation presenting as vaginal bleeding following vaginal delivery in a 23-year-old woman: A case report.

Afaf Alsharif, Saif Ghabisha, Faisal Ahmed, Mohamed Badheeb

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Article in Case reports in women's health, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Afaf AlsharifDepartment of Gynecology, School of Medicine, Jeblah University for Medical and Health Sciences, Ibb, Yemen.
Saif GhabishaDepartment of General Surgery, School of Medicine, Ibb University of Medical Sciences, Ibb, Yemen.
Faisal AhmedDepartment of Urology, School of Medicine, Ibb University of Medical Sciences, Ibb, Yemen.
Mohamed BadheebDepartment of Internal Medicine, College of Medicine, Hadhramaut University, Mukalla, Yemen.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital uterine arteriovenous malformations (AVMs) are an uncommon cause of vaginal bleeding in women of reproductive age. In the medical literature, there are few reports of congenital uterine AVMs. This report describes a 23-year-old woman who presented with intermittent vaginal bleeding following a vaginal delivery two years prior. Initially, a molar pregnancy was suspected, but further assessment with magnetic resonance imaging revealed a diagnosis of right uterine AVM. The patient underwent uterine artery embolization, which was repeated three months later. At two-year follow-up, the patient remained free of symptoms. This case highlights the importance of considering congenital uterine AVM as a potential cause of vaginal bleeding and emphasizes the need for clinical examination and radiologic investigations to establish an accurate diagnosis. Treatment depends on disease severity, comorbidities, patient age, and fertility desires.

Indexed as

Arterial embolizationCase reportCongenital uterine arteriovenous malformationVaginal bleedingVaginal delivery

Identifiers

PMID36915294
PMCPMC10006706

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