Evidence map›Paper›PMID 37937910›Full record

ArticleRevista colombiana de obstetricia y ginecologia2023

Thoracic kidney and diaphragmatic hernia: prenatal diagnosis and successful management. Case report and review of the literature

Mario Fernando Ortega-Mafla, Valerye Viveros-Gonzalez, Wilmar Saldarriaga-Gil

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Article in Revista colombiana de obstetricia y ginecologia, 2023. 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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0citing papers in PubMed
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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

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

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0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

3 authors at 2 institutions in 1 country.

Mario Fernando Ortega-MaflaClínica Farallones, Cali (Colombia).. mfortegam@hotmail.com.ORCID 0009-0000-4772-2607
Valerye Viveros-GonzalezUniversidad del Valle, Cali (Colombia). . valerye.viveros@correounivalle.edu.co.ORCID 0009-0006-3715-374X
Wilmar Saldarriaga-GilUniversidad del Valle, Cali (Colombia).. wilmar.saldarriaga@correounivalle.edu.co.ORCID 0000-0001-7815-4390
Universidad del Valle · COFundación para la Educación y el Desarrollo Social · CO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: To report a case of prenatal diagnosis of ectopic intrathoracic kidney with diaphragmatic hernia managed surgically after birth, and to conduct a review of the literature on prenatal diagnosis of ectopic intrathoracic kidney and perinatal prognosis. Material and methods: We report the case of a 28-week fetus in which, on ultrasound imaging, a mass was observed displacing the heart and lung in the right hemithorax, which was was confirmed by magnetic resonance (MR) to be an ectopic intrathoracic kidney (ITEK). After birth, the neonate was approached by laparoscopy to place a mesh in continuity with the diaphragm, leaving the kidney in the abdomen, with good evolution. A search was conducted in the PubMed, Embase and Cochrane databases for cohorts, case reports and case series of prenatal diagnosis of intrathoracic kidney in the fetus. Information was retrieved regarding design, population, imaging diagnosis, treatment and prognosis. Results: The search identified 8 studies that met the inclusion criteria, reporting a total of 8 cases. Ultrasound diagnosis showed ectopic intrathoracic kidney associated with diaphragmatic hernia in all the subjects. Fetal magnetic resonance imaging (MRI) was also used in 5 cases. Conclusions: Ectopic intrathoracic kidney is a congenital abnormality amenable to prenatal diagnosis. Survival after corrective surgery performed in the neonatal period is common. There is a paucity of publications, limited to case reports, regarding the prenatal diagnosis of this condition.

Indexed as

Hernia, DiaphragmaticPrenatal DiagnosisFemaleHerniaHumansInfant, NewbornKidneyPregnancyCongenital diaphragmatic herniakidneyprenatal diagnosisurogenital abnormalities

Identifiers

PMID37937910
PMCPMC10652776
OpenAlexW4387445993

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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.