Evidence map›Paper›PMID 28078671›Full record

ReviewThe British journal of dermatology2017

Melanoma in congenital melanocytic naevi.

V A Kinsler, P O'Hare, N Bulstrode, J E Calonje, W K Chong, D Hargrave, T Jacques, D Lomas, N J Sebire, O Slater

Open access · hybridAbstract readReview
In one paragraph

Review in The British journal of dermatology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 2 pooled it
10.7field-weighted citation impact, top 1% 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

78 citing papers in PubMed, 2 syntheses or guidelines pooled it, 230 citations in OpenAlex.

  1. Pooled it
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  6. Molecular pathology in the diagnosis of cutaneous melanoma.Pathologie (Heidelberg, Germany) · 2026
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18 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

V A KinslerPaediatric Dermatology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, U.K.
P O'HarePaediatric Oncology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, U.K.
N BulstrodePaediatric Plastic Surgery, Great Ormond Street Hospital for Children NHS Foundation Trust, London, U.K.
J E CalonjeDermatopathology Department, St John's Institute of Dermatology, Guy's and St Thomas' Hospital, London, U.K.
W K ChongPaediatric Neuroradiology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, U.K.
D HargravePaediatric Oncology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, U.K.
T JacquesHistopathology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, U.K.
D LomasPaediatric Dermatology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, U.K.
N J SebireHistopathology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, U.K.
O SlaterPaediatric Oncology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, U.K.
Great Ormond Street Hospital for Children NHS Foundation Trust · GBUniversity College London · GBSt Thomas' Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital melanocytic naevi (CMN) are a known risk factor for melanoma, with the greatest risk currently thought to be in childhood. There has been controversy over the years about the incidence of melanoma, and therefore over the clinical management of CMN, due partly to the difficulties of histological diagnosis and partly to publishing bias towards cases of malignancy. Large cohort studies have demonstrated that melanoma risk in childhood is related to the severity of the congenital phenotype. New understanding of the genetics of CMN offers the possibility of improvement in diagnosis of melanoma, identification of those at highest risk, and new treatment options. We review the world literature and our centre's experience over the last 25 years, including the molecular characteristics of melanoma in these patients and new melanoma incidence and outcome data from our prospective cohort. Management strategies are proposed for presentation of suspected melanoma of the skin and the central nervous system in patients with CMN, including use of oral mitogen-activated protein kinase kinase inhibitors in NRAS-mutated tumours.

Indexed as

Brain NeoplasmsChildChild, PreschoolFemaleGTP PhosphohydrolasesHumansInfantMaleMelanomaMembrane ProteinsMitogen-Activated Protein Kinase KinasesMosaicismMutationNevus, PigmentedRisk FactorsSkin NeoplasmsGTP PhosphohydrolasesMembrane ProteinsMitogen-Activated Protein Kinase KinasesNRAS protein, human

Identifiers

PMID28078671
PMCPMC5484991
OpenAlexW2574407041

What OpenQuestion holds

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LicenceCC BY
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.