Evidence map›Paper›PMID 41975061›Full record

ArticlePathologie (Heidelberg, Germany)2026

[A cutaneous lesion of the axilla: an (un)common diagnosis].

Sarah Theurer, Sabrina Borchert, Elisabeth Bednaric, Hideo A Baba, Lutz Schmitz

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

Article in Pathologie (Heidelberg, Germany), 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

5 authors.

Sarah TheurerInstitut für Pathologie, Universitätsklinikum Essen, Universität Duisburg-Essen, Hufelandstr. 55, 45147, Essen, Deutschland. sarah.theurer@uk-essen.de.ORCID http://orcid.org/0000-0002-8783-5558
Sabrina BorchertInstitut für Pathologie, Universitätsklinikum Essen, Universität Duisburg-Essen, Hufelandstr. 55, 45147, Essen, Deutschland.
Elisabeth BednaricInstitut für Pathologie, Universitätsklinikum Essen, Universität Duisburg-Essen, Hufelandstr. 55, 45147, Essen, Deutschland.
Hideo A BabaInstitut für Pathologie, Universitätsklinikum Essen, Universität Duisburg-Essen, Hufelandstr. 55, 45147, Essen, Deutschland.
Lutz SchmitzDermatohistopathologie Centroderm, Wuppertal, Deutschland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A 21-year-old female presented with a 1 cm red, polypoid cutaneous tumor near the axilla that was surgically excised. Histomorphology revealed a subepithelial tumor with features suggestive of a granular cell tumor; however, immunohistochemistry for S100 and SOX10 was negative. Further analysis showed immunohistochemical ALK positivity, and Archer-based molecular testing identified a KLC1-ALK fusion (KLC1 exon 3-ALK exon 20). These findings supported the diagnosis of a cutaneous non-neural granular cell tumor, a rare cutaneous neoplasm that mimics conventional granular cell tumors histomorphologically but lacks their typical immunophenotype and commonly harbors ALK fusions.

Indexed as

AxillaGranular Cell TumorSkin NeoplasmsAnaplastic Lymphoma KinaseDiagnosis, DifferentialFemaleHumansImmunohistochemistryReceptor Protein-Tyrosine KinasesYoung AdultALK protein, humanAnaplastic Lymphoma KinaseReceptor Protein-Tyrosine KinasesALK fusionCutaneous non-neuronal granular cell tumorGranular cell tumorPrimitive polypoid granular cell tumorSkin tumor

Identifiers

PMID41975061
PMCPMC13503479

What OpenQuestion holds

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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.