Evidence map›Paper›PMID 33040161›Full record

ArticleVirchows Archiv : an international journal of pathology2021

Expanding spectrum of "spitzoid" lesions: a small series of 4 cases with MAP2K1 mutations.

K G P Kerckhoffs, T Aallali, C A Ambarus, V Sigurdsson, A M L Jansen, W A M Blokx

Abstract readCase Reports
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Gene fusions in melanocytic lesions: an updated comprehensive review.Journal of pathology and translational medicine · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Conceptual Evolution and Current Approach to Spitz Tumors.Dermatopathology (Basel, Switzerland) · 2022
    Article
  7. The Morpho-Molecular Landscape of Spitz Neoplasms.International journal of molecular sciences · 2022
    Review
  8. 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

6 authors.

K G P KerckhoffsDepartment of Pathology, Maastricht University Medical Center+, Maastricht, The Netherlands. kelly.kerckhoffs@mumc.nl.ORCID http://orcid.org/0000-0002-3108-6412
T AallaliSymbiant Pathology Expert Center, Hoorn/Zaandam, The Netherlands.
C A AmbarusDepartment of Pathology, Sint Antonius Hospital, Nieuwegein, The Netherlands.
V SigurdssonDepartment of Dermatology, University Medical Center Utrecht, Utrecht, The Netherlands.
A M L JansenDepartment of Pathology, Division of Laboratories, Pharmacy and Biomedical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
W A M BlokxDepartment of Pathology, Division of Laboratories, Pharmacy and Biomedical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The molecular background of a significant proportion of spitzoid neoplasms is still unknown. Recently, activating mutations in MAP2K1 have been described in a few spitzoid lesions, but not in benign Spitz nevi. We report four cases of melanocytic tumors with spitzoid features in which a MAP2K1 mutation was detected. The lesions did not show a single distinct phenotype and ranged from benign to malignant. Two cases resembled desmoplastic Spitz nevi. Based on the combination of morphological, immunohistochemical, and molecular findings, one case was classified as benign, one as probably benign, possibly intermediate low-grade (MELTUMP-melanocytic tumor of unknown malignant potential), one case was classified as intermediate (MELTUMP), and one case was considered a superficial spreading melanoma with spitzoid features. Based on this, we conclude that MAP2K1 mutations can indicate a spitzoid genetic signature and can be found in both benign and malignant spitzoid neoplasms.

Indexed as

MutationAdolescentAgedBiomarkers, TumorFemaleGenetic Predisposition to DiseaseHumansMaleMAP Kinase Kinase 1MelanomaMiddle AgedNevus, Epithelioid and Spindle CellPhenotypeSkin NeoplasmsBiomarkers, TumorMAP2K1 protein, humanMAP Kinase Kinase 1MAP2K1MelanomaMELTUMPSpitz nevus

Identifiers

PMID33040161
PMCPMC8298358

What OpenQuestion holds

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Registered trials

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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.