Evidence map›Paper›PMID 40206325›Full record

ArticleCase reports in dentistry2025

Nonsyndromic Extraosseous Palate Neurofibroma of a 30-Year-Old Woman: A Case Report.

Fahimeh Akhlaghi, Fatemeh Mashhadiabbas, Milad Baseri, Sanaz Gholami Toghchi, Maryam Mohammadalizadeh Chafjiri, Ardeshir Khorsand

Abstract readCase Reports
In one paragraph

Article in Case reports in dentistry, 2025. 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

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

6 authors.

Fahimeh AkhlaghiDepartment of Oral and Maxillofacial Surgery, Dentistry Faculty, Shahid Beheshti University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0003-0352-8831
Fatemeh MashhadiabbasDepartment of Oral and Maxillofacial Pathology, Dentistry Faculty, Shahid Beheshti University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0003-3789-1727
Milad BaseriDepartment of Oral and Maxillofacial Surgery, Dentistry Faculty, Shahid Beheshti University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0001-8531-8699
Sanaz Gholami ToghchiDepartment of Oral and Maxillofacial Pathology, Dentistry Faculty, Shahid Beheshti University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0002-6823-6509
Maryam Mohammadalizadeh ChafjiriDepartment of Oral and Maxillofacial Pathology, Dentistry Faculty, Shahid Beheshti University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0002-1889-0553
Ardeshir KhorsandDepartment of Oral and Maxillofacial Surgery, Dentistry Faculty, Shahid Beheshti University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0002-0618-4387

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurofibroma (NF) is a benign peripheral nerve sheath tumor which consists of Schwann cells, perineurial-like cells, and fibroblasts. The NF can be central or peripheral, alone or multiple which is a manifestation of Type I neurofibromatosis. NFs are mostly found in the tongue, oral mucosa, and lips when appearing in the mouth cavity, but they are rare at palate in a solitary form. We report a case of a solitary NF originating in the hard palate in a 30-year-old woman. The patient had an asymptomatic, nonulcerated, sessile, pink, and smooth nodule measuring 15 × 25 × 5 mm with a firm consistency and defined border on the left side of the posterior part of the hard palate. She had a similar history about 12 years ago which was diagnosed as a benign myxoid tumor which was excised that time. The lesion was excised with a 3-mm safe margin. The periosteum was excised, but the palatal bone was intact and was not excised. IHC was positive for S-100 immunostaining. Eventually, the mass was diagnosed as a NF. The important point is that following the patient with NF is necessary, because it could be the primary sign of Type I neurofibromatosis. The follow-up of this patient is continuing, and until the accomplishment of this report, no relapse was evident.

Indexed as

neurofibromapalatesoft tissuesolitary

Identifiers

PMID40206325
PMCPMC11981700

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