Evidence map›Paper›PMID 36227346›Full record

ReviewPathologie (Heidelberg, Germany)2022

[Salivary gland tumors-an overview : Advances in molecular characterization: Part I].

Niels J Rupp, Sandra N Freiberger

Open access · hybridAbstract readReviewEnglish Abstract
In one paragraph

Review in Pathologie (Heidelberg, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 76% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

2 authors at 2 institutions in 1 country.

Niels J RuppInstitut für Pathologie und Molekularpathologie, Universitätsspital Zürich, Universität Zürich, Zürich, Schweiz. niels.rupp@usz.ch.
Sandra N FreibergerInstitut für Pathologie und Molekularpathologie, Universitätsspital Zürich, Universität Zürich, Zürich, Schweiz.
University Hospital of Zurich · CHUniversity of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, the characterization of salivary gland tumors has undergone a major transformation. Morphologically defined entities could to a large extent also be characterized molecularly with an often distinct genotype. The first part of this article reviews the advances in the molecular characteristics of mucoepidermoid carcinoma, adenoid cystic carcinoma, acinic cell carcinoma, secretory carcinoma, intraductal carcinoma, and hyalinizing clear cell carcinoma. The molecular genotype can be particularly useful in classifying unusual morphologic variants. Recurrent NTRK or RET gene fusions can be used not only as a diagnostic tool but also for potential targeted therapy.

Indexed as

Carcinoma, Acinar CellCarcinoma, Adenoid CysticCarcinoma, Intraductal, NoninfiltratingCarcinoma, MucoepidermoidSalivary Gland NeoplasmsHumansClassificationGene fusionMorphological and microscopic findingsMutationSalivary gland neoplasms

Identifiers

PMID36227346
PMCPMC9584877
OpenAlexW4304959158

What OpenQuestion holds

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LicenceCC BY
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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.