Evidence map›Paper›PMID 41377902›Full record

ArticleIranian journal of medical sciences2025

Congenital Palatal Teratoma: A Rare Case of Postnatal Diagnosis and Multidisciplinary Management.

Nona Sabeti, Ezat Hajmollarezaei, Ahmad Mohamad Pour, Emad Pour Rajab

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PubMed Full text at PMC Publisher
In one paragraph

Article in Iranian journal of medical sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

0 citing papers in PubMed.

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

4 authors.

Nona SabetiSupporting the Family and the Youth of Population Research Core, Department of Obstetrics and Gynecology, School of Medicine, Mashhad University of Medical Science, Mashhad, Iran.
Ezat HajmollarezaeiSupporting the Family and the Youth of Population Research Core, Department of Obstetrics and Gynecology, School of Medicine, Mashhad University of Medical Science, Mashhad, Iran.
Ahmad Mohamad PourDepartment of Pediatric Surgery, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Emad Pour RajabDepartment of Pediatric Surgery, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oropharyngeal teratoma (OPT) is a rare congenital tumor that may present either in isolation or in conjunction with craniofacial anomalies, often posing a major risk to infant survival. Recent advances in prenatal imaging, particularly high-resolution ultrasonography, have significantly improved the early detection and characterization of such tumors, enhancing clinical decision-making. Although prenatal sonography and MRI typically enable early diagnosis, the present study reported a case of OPT, diagnosed postpartum in an Iranian female infant weighing 4300 g. Despite the absence of prenatal diagnosis, the mass was successfully managed through prompt surgical intervention. The outcome was favorable, with no complications or recurrence. This case highlighted the critical role of early diagnosis and multidisciplinary perinatal planning in improving the prognosis of rare congenital tumors such as OPT.

Indexed as

TeratomaAdultFemaleHumansInfant, NewbornMagnetic Resonance ImagingPregnancyUltrasonography, PrenatalCongenital abnormalitiesOropharyngeal neoplasmsPrenatal diagnosisTeratomaUltrasonography

Identifiers

PMID41377902
PMCPMC12686947

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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.