Evidence map›Paper›PMID 32632899›Full record

ArticlePathology oncology research : POR2020

A Clinicopathological Approach to Odontogenic Cysts: the Role of Cytokeratin 17 and bcl2 Immunohistochemistry in Identifying Odontogenic Keratocysts.

Dorottya Cserni, Tamás Zombori, András Vörös, Anette Stájer, Annamária Rimovszki, Krisztián Daru, Zoltán Baráth, Gábor Cserni

Abstract 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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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.

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.ORCID https://orcid.org/0000-0002-0654-563X
András VörösDepartment 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.ORCID https://orcid.org/0000-0003-4158-173X
Annamária RimovszkiDepartment of Pathology, Bács-Kiskun County Teaching Hospital, Nyíri út 38, Kecskemét, H-6000, Hungary.
Krisztián DaruDepartment of Pathology, University of Szeged, Állomás u. 1, Szeged, H-6725, Hungary.
Zoltán BaráthDepartment of Prosthodontics, Faculty of Dentistry, University of Szeged, Tisza Lajos krt 64-66, Szeged, H-6720, Hungary.ORCID https://orcid.org/0000-0003-0636-6313
Gábor CserniDepartment of Pathology, University of Szeged, Állomás u. 1, Szeged, H-6725, Hungary. cserni@freemail.hu.ORCID https://orcid.org/0000-0003-1344-7744

Funding

National Research, Development and Innovation Office GINOP-2.3.2-15-2016-00020
6 · The paper itself

Abstract

Odontogenic keratocysts (OKCs) are developmental cysts of the jaws that require proper diagnosis due to their potential for local aggressive growth and recurrences. OKCs have a typical parakeratotic epithelium demonstrating transepithelial cytokeratin 17 (CK17) and basal bcl2 staining on immunohistochemistry (IHC), which distinguishes them from other common jaw cysts. Secondary to inflammation, the epithelial lining may be altered and loses the typical IHC phenotype. The aim of the present study was to analyse a series of consecutive jaw cysts for their expression of CK17 and bcl2 and assess how these IHC stains may help in their diagnosis. All cysts were retrospectively assessed for available clinical, radiological and pathological findings and diagnoses were revised whenever needed. 85 cysts from 72 patients were collected from two departments. The series had 21 OKCs, the remaining non-OKCs included radicular/residual, dentigerous, paradental, lateral periodontal, botryoid odontogenic cysts. OKCs with typical epithelium showed the typical IHC phenotype, which was generally lost in inflammation-associated altered epithelium. Contrarily to earlier descriptions, a wide variety of CK17 positivity was seen in the majority of non-OKCs, including focal transepithelial staining. Basal bcl2 staining was also seen in 16 non-OKCs. These stainings were never as strong in intensity as seen in OKCs. One case was histopathologically identified as OKC due to focally maintained IHC profile. CK17 and bcl2 IHC may help in the diagnosis of OKCs, but must be interpreted with caution and is not a yes or no tool in the diagnostic puzzle.

Indexed as

AdolescentAdultAgedBiomarkersCase-Control StudiesChildFemaleFollow-Up StudiesHumansImmunohistochemistryKeratin-17MaleMiddle AgedOdontogenic CystsPrognosisProto-Oncogene Proteins c-bcl-2BCL2 protein, humanBiomarkersKeratin-17KRT17 protein, humanProto-Oncogene Proteins c-bcl-2B cell lymphoma – 2 (bcl2)Cytokeratin 17Dentigerous cystOdontogenic keratocystRadicular cyst

Identifiers

PMID32632899
PMCPMC7471163

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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.