Evidence map›Paper›PMID 25342144›Full record

ArticleVirchows Archiv : an international journal of pathology2015

NRAS-mutated melanocytic BAP1-associated intradermal tumor (MBAIT): a case report.

Willeke A M Blokx, Katrin Rabold, H Jorn Bovenschen, Marjolijn J L Ligtenberg, Arjen R Mensenkamp, Gesina van Lijnschoten, Wendy A G van Zelst-Stams, Patricia J T A Groenen

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In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

3 citing papers in PubMed, 13 citations in OpenAlex.

  1. Molecular pathology in the diagnosis of cutaneous melanoma.Pathologie (Heidelberg, Germany) · 2026
    Review
  2. Amplification of Mutant NRAS in Melanocytic Tumors With Features of Spitz Tumors.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2024
    Article
  3. Novel insights into the BAP1-inactivated melanocytic tumor.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2022
    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 at 4 institutions in 1 country.

Willeke A M BlokxDepartment of Pathology, Radboud University Medical Center, P.O. Box 9101, Nijmegen, The Netherlands, willeke.blokx@radboudumc.nl.
Katrin Rabold
H Jorn Bovenschen
Marjolijn J L Ligtenberg
Arjen R Mensenkamp
Gesina van Lijnschoten
Wendy A G van Zelst-Stams
Patricia J T A Groenen
Radboud University Medical Center · NLRadboud University Nijmegen · NLMáxima Medisch Centrum · NLPAMM · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melanocytic BAP1-associated intradermal tumors (MBAITs) are epithelioid spitzoid looking, mostly intradermally located melanocytic tumors that often have tumor-infiltrating lymphocytes and a common nevus component. They occur sporadically but also in the context of an underlying BAP1 germline mutation. Recognition of these lesions is important because they can be a marker for an underlying BAP1-associated cancer syndrome. Most cases reported in the literature thus far were found to have both a BRAF and BAP1 mutation. Here, we report an unusual case of an MBAIT lesion with a combined NRAS and BAP1 mutation. A BAP1 germline mutation was excluded. Our case is the second case reported until now with this combination of mutations in this subset of lesions. In the other reported NRAS-/BAP1-mutated MBAIT case, presence of a BAP1 germline mutation was not tested. Our case confirms that the mutational spectrum in MBAITs is broader than previously thought. Just as in the BRAF-mutated cases, it is likely that a subset might be associated with a BAP1 germline mutation. In case of suspicion of an MBAIT lesion based on histological examination, diagnostic work-up should include assessment of protein expression and/or mutation analysis of at least BRAF, NRAS, and BAP1. Work-up should not be limited to analyzing only BRAF protein expression or mutation, since NRAS-mutated MBAITs might be missed.

Indexed as

AdultBiomarkers, TumorDermatologic Surgical ProceduresGene Expression Regulation, NeoplasticGTP PhosphohydrolasesHumansMaleMembrane ProteinsMutationNevus, IntradermalNevus, PigmentedProto-Oncogene Proteins B-rafSkinSkin NeoplasmsTumor Suppressor ProteinsUbiquitin ThiolesteraseBAP1 protein, humanBiomarkers, TumorBRAF protein, humanGTP PhosphohydrolasesMembrane ProteinsNRAS protein, humanProto-Oncogene Proteins B-rafTumor Suppressor ProteinsUbiquitin Thiolesterase

Identifiers

PMID25342144
OpenAlexW2006247095

What OpenQuestion holds

Textmetadata
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.