Evidence map›Paper›PMID 31628579›Full record

ArticlePathology oncology research : POR2020

Immunohistochemical Characterization of Reactive Epithelial Changes in Odontogenic Keratocysts.

Dorottya Cserni, Tamás Zombori, Anette Stájer, Annamária Rimovszki, Gábor Cserni, Zoltán Baráth

Open access · hybridAbstract read
In one paragraph

Article in Pathology oncology research : POR, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Dorottya CserniDepartment of Prosthodontics, Faculty of Dentistry, University of Szeged, Tisza Lajos krt 64-66., Szeged, H-6720, Hungary.
Tamás ZomboriDepartment of Pathology, University of Szeged, Állomás u. 1, Szeged, H-6725, Hungary.
Anette StájerDepartment of Prosthodontics, Faculty of Dentistry, University of Szeged, Tisza Lajos krt 64-66., Szeged, H-6720, Hungary.
Annamária RimovszkiDepartment of Pathology, Bács-Kiskun County Teaching Hospital, Nyíri út 38, Kecskemét, H-6000, Hungary.
Gábor CserniDepartment of Pathology, University of Szeged, Állomás u. 1, Szeged, H-6725, Hungary. cserni@freemail.hu.ORCID http://orcid.org/0000-0003-1344-7744
Zoltán BaráthDepartment of Prosthodontics, Faculty of Dentistry, University of Szeged, Tisza Lajos krt 64-66., Szeged, H-6720, Hungary.
University of Szeged · HUBács-Kiskun Megyei Kórház · HU

Funding

Nemzeti Kutatási Fejlesztési és Innovációs Hivatal GINOP-2.3.2-15-2016-00020
6 · The paper itself

Abstract

Odontogenic keratocysts (OKCs) have a diagnostic thin epithelial lining characterised by a linear epithelial connective tissue interface generally lacking inflammatory changes, basal palisading of the nuclei and a wavy parakeratotic layer on the surface. This typical epithelium may convert to a thicker non-keratinizing one with rete pegs and a relatively flat surface after operative decompression. The aim was to characterize this type of epithelial change by immunohistochemistry for bcl2, keratin17, 10 and 19. Eleven out of 33 archived OKCs demonstrated an altered epithelium related to previous biopsy, decompressing drainage or inflammation. The typical basal bcl2 staining was lost in 10/11 cases; transepithelial CK17 was lost or markedly reduced in 9/11 cases. CK10 displayed a segmental upper layer staining in OKCs, and its loss or partial loss in the altered epithelium did not differ from negative areas of OKCs. CK19 displayed various staining patterns in the altered epithelium from lost to maintained in a patchy transepithelial distribution, the latter of which did not differ from the typical OKC staining pattern. Three of four non-keratinizing epithelial linings with basal palisading displayed immunostaining reminiscent of typical OKC epithelium. The lack of a typical epithelium is not sufficient to exclude the diagnosis of OKC if the sampling is not generous (e.g. biopsy), and the presence of non-keratinizing epithelium with basal palisading and an immunophenotype characteristic of OKC (basal bcl2, patchy or diffuse CK17 and upper layer CK10 positivity) may be consistent with the OKC diagnosis even in the absence of typical epithelial lining.

Indexed as

AdolescentAdultAgedBiomarkersChildEpitheliumFemaleHumansImmunohistochemistryMaleMiddle AgedOdontogenic CystsYoung AdultBiomarkersbcl2Cytokeratin 10Cytokeratin 17Cytokeratin 19ImmunohistochemistryOdontogenic keratocyst

Identifiers

PMID31628579
PMCPMC7297854
OpenAlexW2980776416

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.