Evidence map›Paper›PMID 35371381›Full record

ArticleThe Pan African medical journal2022

Polysplenia syndrome in adulthood: a case report.

Manal Cherkaoui Malki, Mustapha Outznit, Salma Mechhor, Boutaina Bouibaouen, Lambert Nkurunziza, Hicham El Bacha, Nadia Benzzoubeir, Fatime Zahrae Laamrani, Laila Jroundi, Ikram Errabih

Open access · goldAbstract readCase Reports
In one paragraph

Article in The Pan African medical journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 18% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

10 citing papers in PubMed, 12 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

Manal Cherkaoui MalkiDepartment of Gastroentero-Hepatology and Proctology "Médecine B" department, University Hospital Ibn Sina, Rabat, Morocco.
Mustapha OutznitEmergency Radiology Department, University Hospital Ibn Sina, Rabat, Morocco.
Salma MechhorDepartment of Gastroentero-Hepatology and Proctology "Médecine B" department, University Hospital Ibn Sina, Rabat, Morocco.
Boutaina BouibaouenDepartment of Gastroentero-Hepatology and Proctology "Médecine B" department, University Hospital Ibn Sina, Rabat, Morocco.
Lambert NkurunzizaDepartment of Gastroentero-Hepatology and Proctology "Médecine B" department, University Hospital Ibn Sina, Rabat, Morocco.
Hicham El BachaDepartment of Gastroentero-Hepatology and Proctology "Médecine B" department, University Hospital Ibn Sina, Rabat, Morocco.
Nadia BenzzoubeirDepartment of Gastroentero-Hepatology and Proctology "Médecine B" department, University Hospital Ibn Sina, Rabat, Morocco.
Fatime Zahrae LaamraniEmergency Radiology Department, University Hospital Ibn Sina, Rabat, Morocco.
Laila JroundiEmergency Radiology Department, University Hospital Ibn Sina, Rabat, Morocco.
Ikram ErrabihDepartment of Gastroentero-Hepatology and Proctology "Médecine B" department, University Hospital Ibn Sina, Rabat, Morocco.
Centre Hospitalier Ibn Sina · MA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polysplenia syndrome mainly described in pediatrics; rarely and incidentally in adulthood. Most patients had their diagnosis done during childhood due to the frequent association to cardiac anomalies that speak for themselves earlier in life. Multiple spleens, cardiac defect and vascular malformation of the inferior vena cava with azygos or hemiazygos continuation are the most frequent observed malformations. Our patient was one this rarest adulthood incidental diagnosis, who presented in the emergency department for nephritic colic, and while imaging for this, multiples spleens and other visceral malformations were diagnosed. Hopefully, cardiac ultrasound hadn't showed any cardiac malformation and the patient was discharged aware of this condition. Through this publication we report the possible incidental diagnosis of polysplenia condition and highlight the fact that people with such important malformation can lead a normal life, and only awareness should be given for future surgeries, instrumental treatment or else.

Indexed as

Heterotaxy SyndromeAdultChildEchocardiographyHumansVena Cava, Inferioradultcase reportincidentalmalformationsPolysplenia

Identifiers

PMID35371381
PMCPMC8933446
OpenAlexW4207037915

What OpenQuestion holds

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Registered trials

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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.