Evidence map›Paper›PMID 36510447›Full record

ArticleThe Journal of international medical research2022

A fortuitous discovery of a neurofibroma in a female patient with type 1 neurofibromatosis: a case report.

Fathia Harrabi, Jabeur Methnani, Ammar Houssem, Mizouni Abdelkader, Ben Latifa Mehdi, Saiid Mohamed Amine, Ben Mabrouk Mohamed, Ben Ali Ali

Open access · goldAbstract readCase Reports
In one paragraph

Article in The Journal of international medical research, 2022. 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, top 76% 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

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

8 authors at 1 institution in 1 country.

Fathia HarrabiDepartment of General Surgery, Sahloul University Hospital, Sousse, Tunisia.
Jabeur MethnaniLR12SP11, Biochemistry Department, Sahloul University Hospital, Sousse, Tunisia.ORCID 0000-0002-1422-3059
Ammar HoussemDepartment of General Surgery, Sahloul University Hospital, Sousse, Tunisia.
Mizouni AbdelkaderDepartment of General Surgery, Sahloul University Hospital, Sousse, Tunisia.
Ben Latifa MehdiDepartment of General Surgery, Sahloul University Hospital, Sousse, Tunisia.
Saiid Mohamed AmineDepartment of General Surgery, Sahloul University Hospital, Sousse, Tunisia.
Ben Mabrouk MohamedDepartment of General Surgery, Sahloul University Hospital, Sousse, Tunisia.
Ben Ali AliDepartment of General Surgery, Sahloul University Hospital, Sousse, Tunisia.
Hôpital Sahloul · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurofibromatosis type 1 (NF1) is a neurocutaneous condition with an autosomal dominant pattern of inheritance. This congenital disease is characterized by a wide spectrum of clinical manifestations and degree of severity. This case report describes a female patient in her early 20s who presented with a complaint of lumbosciatica-like pain evolving for several months. The condition initially escaped the attention of clinicians until a lumbar computed tomography scan and spinal magnetic resonance imaging were performed. The patient was then transferred to the general surgery department, where a clinical diagnosis of NF1 was established. The clinical manifestations were specific for this disease, including café-au-lait macules, plexiform neurofibroma, and a history of neurofibromatosis in her mother. The patient underwent surgical resection of the neurofibroma, which resulted in a favorable outcome. However, 2 years later, a new mass attached to the second lumbar spinal nerve was revealed by a follow-up computed tomography scan. Long-term and close follow-up of NF1 is required because of the high risk of malignancy and recurrence in NF1 patients.

Indexed as

NeurofibromaNeurofibromatosesNeurofibromatosis 1Cafe-au-Lait SpotsFemaleHumansMagnetic Resonance Imagingcafé-au-lait maculesNeurofibromatosis type 1NF1plexiform neurofibromaschwannomaVon Recklinghausen disease

Identifiers

PMID36510447
PMCPMC9751173
OpenAlexW4311402316

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.