Evidence map›Paper›PMID 41788126›Full record

ArticleCureus2026

Isolated Anterior Mesenteric Neurofibroma: A Rare Manifestation of Neurofibromatosis Type 1.

Sara Ouassil, Mariem Touraif, Soumia Mrhar, Najoua Aballa, Isaac Mpanya Ntumba, Hussein Choukri Ahmanna, Ibtissam Zouita, Dounia Basraoui, Salma Foura, Mohamed Oulad Saiad and 2 more

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Cureus, 2026. 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

12 authors.

Sara OuassilMother and Child Department, Radiology, University Hospital Center Mohammed VI, Faculty of Medicine and Pharmacy, Cadi Ayyad University, Marrakech, MAR.
Mariem TouraifMother and Child Department, Pediatric Surgery, University Hospital Center Mohammed VI, Faculty of Medicine and Pharmacy, Cadi Ayyad University, Marrakech, MAR.
Soumia MrharMother and Child Department, General Pediatrics, University Hospital Center Mohammed VI, Faculty of Medicine and Pharmacy, Cadi Ayyad University, Marrakech, MAR.
Najoua AballaMother and Child Department, Pediatric Surgery, University Hospital Center Mohammed VI, Faculty of Medicine and Pharmacy, Cadi Ayyad University, Marrakech, MAR.
Isaac Mpanya NtumbaMother and Child Department, General Pediatrics, University Hospital Center Mohammed VI, Faculty of Medicine and Pharmacy, Cadi Ayyad University, Marrakech, MAR.
Hussein Choukri AhmannaMother and Child Department, Radiology, University Hospital Center Mohammed VI, Faculty of Medicine and Pharmacy, Cadi Ayyad University, Marrakech, MAR.
Ibtissam ZouitaMother and Child Department, Radiology, University Hospital Center Mohammed VI, Faculty of Medicine and Pharmacy, Cadi Ayyad University, Marrakech, MAR.
Dounia BasraouiMother and Child Department, Radiology, University Hospital Center Mohammed VI, Faculty of Medicine and Pharmacy, Cadi Ayyad University, Marrakech, MAR.
Salma FouraMother and Child Department, Pediatric Surgery, University Hospital Center Mohammed VI, Faculty of Medicine and Pharmacy, Cadi Ayyad University, Marrakech, MAR.
Mohamed Oulad SaiadMother and Child Department, Pediatric Surgery, University Hospital Center Mohammed VI, Faculty of Medicine and Pharmacy, Cadi Ayyad University, Marrakech, MAR.
Mohammed BouskraouiMother and Child Department, General Pediatrics, University Hospital Center Mohammed VI, Faculty of Medicine and Pharmacy, Cadi Ayyad University, Marrakech, MAR.
Hicham JalalMother and Child Department, Radiology, University Hospital Center Mohammed VI, Faculty of Medicine and Pharmacy, Cadi Ayyad University, Marrakech, MAR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurofibromatosis type 1 (NF1), also known as Von Recklinghausen disease, is a multisystemic, hereditary, autosomal dominant condition. It is caused by the development of tumors in the nervous system, resulting from mutations in the

Indexed as

childgastrointestinal involvementimagingmesenteryneurofibroma

Identifiers

PMID41788126
PMCPMC12959387

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

None linked

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.