Evidence map›Paper›PMID 39572470›Full record

ReviewAmerican journal of clinical dermatology2025

Multiple Keratoacanthomas Associated with Genetic Syndromes: Narrative Review and Proposal of a Diagnostic Algorithm.

Alexandra Dobre, Roxana-Ioana Nedelcu, Gabriela Turcu, Alice Brinzea, Irina Struna, Gabriela Tudorache, Alen Ali, Ionela Hulea, Elena Balasescu, Tudor Emanuel Fertig and 4 more

Erratum issuedAbstract readReview
In one paragraph

Review in American journal of clinical dermatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Mast Cells Are a Reservoir of NLRP1 in Human Skin.International journal of molecular sciences · 2026
    Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Alexandra DobreCarol Davila University of Medicine and Pharmacy, Bucharest, Romania.ORCID http://orcid.org/0000-0001-6052-9027
Roxana-Ioana NedelcuCarol Davila University of Medicine and Pharmacy, Bucharest, Romania. roxanaioana.nedelcu@yahoo.com.ORCID http://orcid.org/0000-0001-7071-527X
Gabriela TurcuCarol Davila University of Medicine and Pharmacy, Bucharest, Romania.ORCID http://orcid.org/0000-0001-5104-6066
Alice BrinzeaCarol Davila University of Medicine and Pharmacy, Bucharest, Romania.ORCID http://orcid.org/0000-0001-7052-2830
Irina StrunaOncologic Dermatology Department, Elias Emergency University Hospital, Bucharest, Romania.
Gabriela TudoracheOncologic Dermatology Department, Elias Emergency University Hospital, Bucharest, Romania.
Alen AliCarol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Ionela HuleaCarol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Elena BalasescuCarol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Tudor Emanuel FertigCarol Davila University of Medicine and Pharmacy, Bucharest, Romania.ORCID http://orcid.org/0000-0003-0251-3865
Mihaela GherghiceanuCarol Davila University of Medicine and Pharmacy, Bucharest, Romania.ORCID http://orcid.org/0000-0001-6117-4328
Catherine HarwoodDepartment of Dermatology, Royal London Hospital, Barts Health NHS Trust, Whitechapel, London, UK.ORCID http://orcid.org/0000-0002-1375-0965
Daniela Adriana Ion *Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.ORCID http://orcid.org/0000-0003-1031-7557
Ana-Maria Forsea *Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.ORCID http://orcid.org/0000-0002-1007-7883

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Keratoacanthoma (KA) is a relatively common, fast-growing epithelial tumour, with characteristic behaviour and clinical variability. Although it appears as a solitary lesion in a majority of cases, multiple KAs do occur, secondary to skin exposure to ultraviolet radiation, chemical carcinogens or certain medications, but may also be associated with various genetic syndromes. Thus, multiple KAs may serve as an early clinical alarm sign. Prompt diagnosis of the underlying cause and identification of the mechanism of development are critical for the secondary prevention of associated organ disorders or neoplasias, the improvement of patient quality of life and familial counselling. Although research in this field has seen important progress in the last few years, there are still many pathogenic processes that have not been elucidated. Additionally, the literature on this topic is limited to individual case reports and small case series, making it difficult for clinicians to parse available data and select the essential information. Therefore, this work aims to review current knowledge, summarizing existing studies, with focus on multiple KAs associated with genetic syndromes, and proposes a diagnostic algorithm for these rare cases to help guide clinicians in their practice. Lastly, we aim to highlight the main gaps in understanding the underlying mechanisms and suggest further research avenues.

Indexed as

KeratoacanthomaSkin NeoplasmsAlgorithmsHumansNeoplastic Syndromes, HereditaryQuality of LifeSkin

Identifiers

PMID39572470
PMCPMC11742465

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.