Evidence map›Paper›PMID 41073541›Full record

ArticleVirchows Archiv : an international journal of pathology2025

Undifferentiated melanoma: a molecular study of a fatal metastatic "atypical fibroxanthoma (AFX)".

Simon Haefliger, Baptiste Ameline, Veronika Blum, Matthias S Matter, Beata Bode-Lesniewska

Abstract readCase Reports
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 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

5 authors.

Simon HaefligerDepartment of Quantitative Biomedicine, University of Zurich, Zurich, Switzerland.
Baptiste AmelinePathology, Institute of Medical Genetics and Pathology, University Hospital of Basel, Basel, Switzerland.
Veronika BlumDepartment of Oncology, Cantonal Hospital Lucerne, Lucerne, Switzerland.
Matthias S Matter *Pathology, Institute of Medical Genetics and Pathology, University Hospital of Basel, Basel, Switzerland.
Beata Bode-Lesniewska *Institute of Pathology, Cantonal Hospital Lucerne, University of Zürich, Spitalstrasse, CH-6000, Lucerne, Switzerland. beata.bode@luks.ch.ORCID http://orcid.org/0000-0002-3329-4186

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diagnosing undifferentiated spindle cell and pleomorphic tumours of the sun-exposed skin of elderly patients is common and challenging. This paper presents the case of a 64-year-old man with a tumour that was initially diagnosed as an atypical fibroxanthoma, but which metastasised to the bone and lung, resulting in death within two years. Extensive comparative molecular studies were performed using next-generation sequencing (NGS) and methylomic analysis, which demonstrated that the skin tumour and the bone metastases corresponded to the same neoplasms. In addition to other aberrations, NGS analysis of both tumour manifestations revealed NF1 gene mutations, suggesting a diagnosis of undifferentiated melanoma. Interestingly, however, the methylomic analysis grouped the tumours with the "atypical fibroxanthoma/pleomorphic dermal sarcoma (AFX/PDS)" class of the reference cases, rather than with conventional or desmoplastic melanomas. Molecular studies may help to reveal the genetic basis of difficult-to-classify undifferentiated skin neoplasms as well as help to estimate their biological potential.

Indexed as

Biomarkers, TumorBone NeoplasmsLung NeoplasmsMelanomaSkin NeoplasmsDNA MethylationFatal OutcomeHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedMutationNeurofibromin 1Biomarkers, TumorNeurofibromin 1NF1 protein, humanAtypical fibroxanthomaMethylomic analysisNext-generation sequencingUndifferentiated melanoma

Identifiers

PMID41073541
PMCPMC12647264

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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.