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The newly proposed International Endocervical Adenocarcinoma Criteria and Classification and its relevance to cervical cytology screening assessed in a prospective 2-year study of 118 cases
O. Ondič, J. Němcová, R. Alaghehbandan, K. Černá, B. Gomolčáková, I. Kinkorová-Luňáčková, J. Chytra, H. Šidlová, M. Hósová, J. Bouda
Language English Country Great Britain
Document type Journal Article
PubMed
32289186
DOI
10.1111/cyt.12831
Knihovny.cz E-resources
- MeSH
- Adenocarcinoma classification diagnosis pathology virology MeSH
- Early Detection of Cancer * MeSH
- Cytodiagnosis methods MeSH
- Uterine Cervical Dysplasia classification diagnosis pathology virology MeSH
- Papillomavirus Infections classification diagnosis pathology virology MeSH
- Humans MeSH
- Papanicolaou Test methods MeSH
- Vaginal Smears methods MeSH
- Check Tag
- Humans MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
BACKGROUND: It is generally acknowledged that interobserver variability for the histological diagnosis of endocervical adenocarcinoma (EA) subtypes is suboptimal. The recently proposed International Endocervical Adenocarcinoma Criteria and Classification (IECC) system is based on the presence of associated human papilloma virus (HPV) infection. It recognises HPV-associated EAs and non-HPV-associated EAs. METHODS: This prospective cytology-histology and molecular genetics-based study investigated the potential effect of IECC being applied to Papanicolaou (Pap) test with regard to the diagnostic accuracy of severe glandular lesions reported at least as adenocarcinoma in situ (AIS). RESULTS: Out of 118 liquid-based cytology Pap tests with AIS+ lesion, complete information on follow-up biopsy and HPV status was available in 51 cases. AIS and EA category correlated with histologically confirmed AIS/EA in 88.5% (23/26) and 70.5% (12/17) of cases, respectively. Interestingly, 93% (40/43) of cases diagnosed as AIS/EA were HPV positive and 7% (3/43) were HPV negative (originating in the cervix, endometrium and adnexa). CONCLUSIONS: Our findings suggest that this approach could possibly divide Pap tests containing severe glandular lesion into two groups: (a) robust diagnosis of HPV-associated EA and (b) non-HPV associated glandular lesions of heterogeneous origin, requiring further clinical preoperative diagnostic workup.
Bioptická laboratoř s r o Pilsen Czech Republic
Cytopathos s r o Bratislava Slovak Republic
Department of Pathology Nemocnice Na Bulovce Praha Czech Republic
Department of Pathology Royal Columbian Hospital University of British Columbia Vancouver BC Canada
Department of Pathology Slovak Medical University Bratislava Slovak Republic
References provided by Crossref.org
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