Evidence map›Paper›PMID 37550584›Full record

ArticleVirchows Archiv : an international journal of pathology2023

MITF::CREM-rearranged tumor: a novel group of cutaneous tumors with melanocytic differentiation.

Antonina Kalmykova, Elaheh Mosaieby, Denisa Kacerovská, Vira Baranovska-Andrigo, Petr Martínek, Sabína Smahová, Michal Michal, Michael Michal

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In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.6field-weighted citation impact, top 11% of its field
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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Gene fusions in melanocytic lesions: an updated comprehensive review.Journal of pathology and translational medicine · 2026
    Article
  4. Article
  5. Review
  6. Review
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 at 3 institutions in 2 countries.

Antonina KalmykovaMedical Laboratory CSD Health Care, Ltd., Kyiv, Ukraine.
Elaheh MosaiebyDepartment of Pathology, Faculty of Medicine in Plzen, Charles University, Plzen, Czech Republic.
Denisa KacerovskáDepartment of Pathology, Faculty of Medicine in Plzen, Charles University, Plzen, Czech Republic.
Vira Baranovska-AndrigoBioptical Laboratory, Ltd., Plzen, Czech Republic.
Petr MartínekDepartment of Pathology, Faculty of Medicine in Plzen, Charles University, Plzen, Czech Republic.
Sabína SmahováDepartment of Pediatric Hematology and Oncology, National Institute of Children's Diseases and Medical Faculty, Comenius University, Bratislava, Slovakia.
Michal MichalDepartment of Pathology, Faculty of Medicine in Plzen, Charles University, Plzen, Czech Republic.
Michael MichalDepartment of Pathology, Faculty of Medicine in Plzen, Charles University, Plzen, Czech Republic. michael.michal@biopticka.cz.ORCID http://orcid.org/0000-0003-4403-7027
Charles University · CZBiopticka Laborator (Czechia) · CZComenius University Bratislava · SK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cutaneous tumors with melanocytic differentiation represent a broad group of neoplasms of both melanocytic and non-melanocytic origin. Besides traditional members such as clear-cell sarcoma (CCS) and PEComa, the latter group has recently expanded to also include MITF::CREM fusion-associated tumors, but the available data are limited. Herein, we present a third case of this rare neoplasm which occurred in the temporal region in a 1-year-old girl. It was an infiltratively growing polypoid dermal-based lesion lacking an intraepidermal component. It consisted of cellular solid sheets or small nests of epithelioid to spindled cells with a predominantly eosinophilic and much less commonly clear cytoplasm. The nuclei had round to ovoid shape and exhibited moderate to high-grade atypia and prominent nucleoli. The mitotic activity was 11 mitoses per 10 high-power fields, and atypical mitotic figures were present. Immunohistochemically, the tumor was strongly positive with S100 protein, SOX10, and MITF, while HMB45, tyrosinase, and Melan A were negative. Extensive molecular analysis revealed only MITF::CREM gene fusion. There had no evidence of disease 9 months after the diagnosis. These tumors need to be distinguished from malignant tumors with melanocytic differentiation, primarily from melanoma. However, additional cases still need to be studied to precisely define their biological potential and establish their nosologic status.

Indexed as

MelanomaSarcoma, Clear CellSkin NeoplasmsBiomarkers, TumorCell DifferentiationCyclic AMP Response Element ModulatorFemaleHumansInfantMelanocytesMicrophthalmia-Associated Transcription FactorBiomarkers, TumorCREM protein, humanCyclic AMP Response Element ModulatorMicrophthalmia-Associated Transcription FactorMITF protein, humanClear-cell sarcoma-likeClear-cell tumorCutaneousMelanocytic differentiationMelanoma-likeMITF::CREM fusionSkin

Identifiers

PMID37550584
OpenAlexW4385661552

What OpenQuestion holds

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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.