Evidence map›Paper›PMID 38467248›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2024

Amplification of Mutant NRAS in Melanocytic Tumors With Features of Spitz Tumors.

Jeffrey M Cloutier, Meng Wang, Swapna S Vemula, Sonia Mirza, Jingly Weier, Jamie D Aquino, Timothy H McCalmont, Philip E LeBoit, Boris C Bastian, Iwei Yeh

Open access · hybridAbstract read
In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Spitz tumours and mimickers.Virchows Archiv : an international journal of pathology · 2025
    Review
  5. 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

10 authors at 2 institutions in 1 country.

Jeffrey M CloutierDepartment of Pathology and Laboratory Medicine, Dartmouth Hitchcock Medical Center, Geisel School of Medicine at Dartmouth, Lebanon, New Hampshire. Electronic address: Jeffrey.Cloutier@dartmouth.edu.
Meng WangDepartment of Dermatology, University of California, San Francisco, California.
Swapna S VemulaDepartment of Dermatology, University of California, San Francisco, California.
Sonia MirzaDepartment of Dermatology, University of California, San Francisco, California.
Jingly WeierDepartment of Dermatology, University of California, San Francisco, California.
Jamie D AquinoDepartment of Pathology, University of California, San Francisco, California.
Timothy H McCalmontDepartment of Dermatology, University of California, San Francisco, California; Department of Pathology, University of California, San Francisco, California; Golden State Dermatology Associates, Walnut Creek, California.
Philip E LeBoitDepartment of Dermatology, University of California, San Francisco, California; Department of Pathology, University of California, San Francisco, California; Helen Diller Family Cancer Center, University of California, San Francisco, California.
Boris C BastianDepartment of Dermatology, University of California, San Francisco, California; Department of Pathology, University of California, San Francisco, California; Helen Diller Family Cancer Center, University of California, San Francisco, California.
Iwei YehDepartment of Dermatology, University of California, San Francisco, California; Department of Pathology, University of California, San Francisco, California; Helen Diller Family Cancer Center, University of California, San Francisco, California. Electronic address: iwei.yeh@ucsf.edu.
University of California, San Francisco · USDartmouth–Hitchcock Medical Center · US

Funding

Molecular and immunologic evolution of melanomas from pre-neoplastic lesionsR35CA220481 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BASTIAN, BORIS C. · 2017 to 2023
$6.3M
NCI NIH HHS R35 CA220481
6 · The paper itself

Abstract

NRAS activating mutations are prevalent in melanocytic neoplasia, occurring in a subset of common acquired melanocytic nevi and ∼30% of cutaneous melanomas. In this study, we described a cohort of 7 distinctive melanocytic tumors characterized by activating point mutations in codon 61 of NRAS with amplification of the mutant NRAS allele and shared clinicopathologic features. These tumors occurred predominantly in younger patients, with a median age of 20 years (range, 6-56 years). They presented as papules on the helix of the ear (4 cases) or extremities (3 cases). Microscopically, the tumors were cellular, relatively well-circumscribed, compound, or intradermal proliferations. The tumor cells often extended into the deep reticular dermis and involved the superficial subcutaneous fat in some cases. The melanocytes were epithelioid to spindled with moderate amounts of cytoplasm and conspicuous nucleoli. They were arranged in short plexiform fascicles, nests, and cords. Some cases had occasional pleomorphic and multinucleated melanocytes. Rare dermal mitotic figures were present in all cases. The dermis contained thick collagen bundles and minimal solar elastosis. Follow-up data were available for 5 patients, with a median period of 4.2 years (range, 1-9 years), during which no recurrences or metastases were reported. Our series highlights a clinicopathologically and molecularly distinctive subset of NRAS-mutated tumors with amplification of the mutant NRAS allele.

Indexed as

GTP PhosphohydrolasesMembrane ProteinsNevus, Epithelioid and Spindle CellSkin NeoplasmsAdolescentAdultChildFemaleGene AmplificationHumansMaleMelanocytesMelanomaMiddle AgedMutationNevus, PigmentedGTP PhosphohydrolasesMembrane ProteinsNRAS protein, humanamplificationmelanocytic tumormelanocytomaNRASSpitzspitzoid

Identifiers

PMID38467248
PMCPMC12970005
OpenAlexW4392655291

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.