Evidence map›Paper›PMID 42071062›Full record

ArticleScientific reports2026

Mutational profile of atypical fibroxanthoma and pleomorphic dermal sarcoma further expands the spectrum of genomic alterations in rare cutaneous neoplasms.

Elisabetta Caprini, Giovanni Luca Scaglione, Claudia Scarponi, Martina Morelli, Stefania Madonna, Carla Marani, Valeria Sebastiani, Enrico Scala, Cristina Albanesi, Siavash Rahimi

Abstract read
In one paragraph

Article in Scientific reports, 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
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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

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

10 authors.

Elisabetta CapriniAnatomic Pathology Unit, Fondazione Luigi Maria Monti, IDI-IRCCS, Via dei Monti di Creta 104, 00167, Rome, Italy. e.caprini@idi.it.
Giovanni Luca ScaglioneBioinformatics Unit, Fondazione Luigi Maria Monti, IDI-IRCCS, Via dei Monti di Creta 104, 00167, Rome, Italy.
Claudia ScarponiExperimental Immunology Laboratory, Fondazione Luigi Maria Monti, IDI-IRCCS, Via dei Monti di Creta 104, 00167, Rome, Italy.
Martina MorelliExperimental Immunology Laboratory, Fondazione Luigi Maria Monti, IDI-IRCCS, Via dei Monti di Creta 104, 00167, Rome, Italy.
Stefania MadonnaExperimental Immunology Laboratory, Fondazione Luigi Maria Monti, IDI-IRCCS, Via dei Monti di Creta 104, 00167, Rome, Italy.
Carla MaraniAnatomic Pathology Unit, Fondazione Luigi Maria Monti, IDI-IRCCS, Via dei Monti di Creta 104, 00167, Rome, Italy.
Valeria SebastianiAnatomic Pathology Unit, Fondazione Luigi Maria Monti, IDI-IRCCS, Via dei Monti di Creta 104, 00167, Rome, Italy.
Enrico ScalaClinical and Laboratory Molecular Allergy Unit, Fondazione Luigi Maria Monti, IDI-IRCCS, Via dei Monti di Creta 104, 00167, Rome, Italy.
Cristina AlbanesiExperimental Immunology Laboratory, Fondazione Luigi Maria Monti, IDI-IRCCS, Via dei Monti di Creta 104, 00167, Rome, Italy.
Siavash RahimiDepartment of Histopathology, The Princess Elizabeth Hospital, Le Vauquiedor, St Martin, GY4 6UU, Guernsey.

Funding

Ministry of Health Ricerca Corrente 2023 and 2024
6 · The paper itself

Abstract

Atypical fibroxanthoma (AFX) and pleomorphic dermal sarcoma (PDS) are rare cutaneous mesenchymal tumours sharing clinical and histopathological features. Compared to AFX, PDS has an increased risk of local recurrence and metastasis. A precise diagnosis is critical to ensure proper clinical management and follow-up. AFX and PDS show a similar genetic background, but also a heterogeneous pattern of different molecular abnormalities still poorly investigated due to the rarity of these tumours. Multiple data from different institutions and geographical areas, facilitate the identification of molecular alteration/s of valuable diagnostic and/or sub-classification power. We investigated the DNA profile of 32 AFX and PDS samples using a custom targeted Next-Generation Sequencing panel including 228 cancer genes. We confirm a common pattern of gene mutations affecting TP53, CDKN2A and NOTCH1. Differences appeared in less frequently detected genes (e.g. TSC2) and in NF2 harbouring novel genetic alterations. Integrating our results with published datasets of AFX and PDS mutation profiles we observed a divergent distribution of alterations in genes signalling through angiogenic pathway (KDR, PDGFRB), DNA damage response (ATR), cellular migration/metastasis (DDR2, CDH1). These differences do not reach statistical significance, and histopathological evaluation remains the diagnostic gold standard, however, they offer valuable insights into the pathogenesis of these tumours.

Indexed as

MutationSarcomaSkin NeoplasmsFemaleHigh-Throughput Nucleotide SequencingHumansMaleATRAtypical fibroxanthomaKDR/PDGFRBNext-generation sequencingNF2Pleomorphic dermal sarcoma

Identifiers

PMID42071062
PMCPMC13332040

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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.