Evidence map›Paper›PMID 40862034›Full record

ArticleCureus2025

A Solitary Diffuse Neurofibroma in a Young Adult Female: An Unusual Presentation in the Scapular Region.

Stephanie Saldaña Guerrero, Talissa F Garza Tovar, Quitzia L Torres

Abstract readCase Reports
In one paragraph

Article in Cureus, 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

3 authors.

Stephanie Saldaña GuerreroDermatology, IMSS Unidad Médica de Alta Especialidad (UMAE) No. 71, Torreón, MEX.
Talissa F Garza TovarDermatology, Universidad Juárez del Estado de Durango, Durango, MEX.
Quitzia L TorresBiomedical Sciences, Universidad Juárez del Estado de Durango, Durango, MEX.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diffuse neurofibroma is a benign peripheral nerve sheath tumor characterized by non-encapsulated spindle cell proliferation within the dermis and subcutaneous tissue. Although usually associated with neurofibromatosis type I (NF1) and preferentially located in the head and neck of pediatric patients, rare instances of sporadic solitary cases in atypical locations have been documented. We describe the case of a 30-year-old female with no personal or familial signs of neurocutaneous syndromes who presented with a two-year history of a slowly enlarging, asymptomatic plaque on the left scapular region. Dermatologic examination revealed an edematous, skin-colored plaque with multiple soft papillary projections. Histopathological analysis showed a poorly circumscribed proliferation of S-shaped spindle cells within a myxoid stroma, consistent with diffuse neurofibroma. Surgical excision was recommended due to infiltrative growth and margin involvement. The presentation of diffuse neurofibroma as a solitary scapular lesion in an adult without stigmata of NF1 is exceptional. Clinical morphology may mimic other benign dermal proliferations, highlighting the importance of histopathological confirmation. The infiltrative behavior and positive margins require complete surgical removal to minimize recurrence risk. Diffuse neurofibroma should be considered in the differential diagnosis of plaque-like lesions with soft nodularity, even in the absence of systemic features of NF1. Histopathologic evaluation is essential for an accurate diagnosis and adequate management planning.

Indexed as

diffuse neurofibromahistopathologyperipheral nerve sheath tumorscapular regionsolitary lesion

Identifiers

PMID40862034
PMCPMC12375364

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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.