Evidence map›Paper›PMID 38132857›Full record

ReviewMetabolites2023

Porokeratoses-A Comprehensive Review on the Genetics and Metabolomics, Imaging Methods and Management of Common Clinical Variants.

Paweł Pietkiewicz, Katarzyna Korecka, Natalia Salwowska, Ihor Kohut, Adarsha Adhikari, Monika Bowszyc-Dmochowska, Anna Pogorzelska-Antkowiak, Cristian Navarrete-Dechent

Abstract readReview
In one paragraph

Review in Metabolites, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Rupioid Porokeratosis on the Lower Leg: An Unprecedented Case Report.Clinical, cosmetic and investigational dermatology · 2026
    Article
  8. Article
  9. Identification of two novelFrontiers in medicine · 2026
    Article
  10. Article
  11. Review
  12. Article
  13. Ultraviolet-Induced Fluorescence Dermoscopy: Game Changers.The Journal of clinical and aesthetic dermatology · 2025
    Article
  14. Article
  15. Article
  16. Article
  17. Porokeratoses: an update on pathogenesis and treatment.International journal of dermatology · 2025
    Review
  18. Porokeratoses-A Rare Group of Dermatoses.Medicina (Kaunas, Lithuania) · 2024
    Review
  19. Article
  20. Article
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

8 authors.

Paweł PietkiewiczDermatology Private Practice, 61-683 Poznan, Poland.ORCID 0000-0001-7262-2456
Katarzyna KoreckaPolish Dermatoscopy Group, 61-683 Poznan, Poland.ORCID 0000-0002-9473-1239
Natalia SalwowskaPolish Dermatoscopy Group, 61-683 Poznan, Poland.
Ihor KohutSkin Health Center, 46027 Ternopil, Ukraine.ORCID 0000-0002-7362-7280
Adarsha AdhikariMedical Private Practice, Pokhara 33700, Nepal.ORCID 0000-0001-7261-478X
Monika Bowszyc-DmochowskaCutaneous Histopathology and Immunopathology Section, Department of Dermatology, Poznan University of Medical Sciences, 60-356 Poznan, Poland.ORCID 0000-0001-8221-7622
Anna Pogorzelska-AntkowiakEsteDerm Private Dermatology Clinic, 43-100 Tychy, Poland.
Cristian Navarrete-DechentMelanoma and Skin Cancer Unit, Department of Dermatology, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.ORCID 0000-0003-4040-3640

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Porokeratosis is a heterogeneous group of keratinising disorders characterised by the presence of particular microscopic structural changes, namely the presence of the cornoid lamella. This structure develops as a consequence of a defective isoprenoid pathway, critical for cholesterol synthesis. Commonly recognised variants include disseminated superficial actinic porokeratosis, disseminated superficial porokeratosis, porokeratosis of Mibelli, palmoplantar porokeratosis (including porokeratosis palmaris et plantaris disseminata and punctate porokeratosis), linear porokeratosis, verrucous porokeratosis (also known as genitogluteal porokeratosis), follicular porokeratosis and porokeratoma. Apart from the clinical presentation and epidemiology of each variant listed, this review aims at providing up-to-date information on the precise genetic background, introduces imaging methods facilitating the diagnosis (conventional and ultraviolet-induced fluorescence dermatoscopy, reflectance confocal microscopy and pathology), discusses their oncogenic potential and reviews the literature data on the efficacy of the treatment used, including the drugs directly targeting the isoprenoid-mevalonate pathway.

Indexed as

dermatoscopygeneticsmalignancymevalonate–isoprenoid pathwayporokeratosisreflectance confocal microscopytreatmentultraviolet radiation

Identifiers

PMID38132857
PMCPMC10744643

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.