Follicular Epithelial Dysplasia as Hashimoto Thyroiditis-Related Atypia: a Series of 91 Specimens
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
X5211
VTR PSHP
2016
Pirkanmaan Syöpäyhdistys
Progres Q28/LF1 (UNCE 204013)
Univerzita Karlova v Praze
Progres Q39
Univerzita Karlova v Praze
PubMed
33991306
PubMed Central
PMC8370905
DOI
10.1007/s12022-021-09679-w
PII: 10.1007/s12022-021-09679-w
Knihovny.cz E-zdroje
- Klíčová slova
- Cytohistologic discrepancy, Fine-needle aspiration, Follicular epithelial dysplasia, Hashimoto thyroiditis, Inflammation, Papillary thyroid carcinoma,
- MeSH
- dospělí MeSH
- Hashimotova nemoc komplikace patologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- nádory štítné žlázy etiologie patologie MeSH
- prekancerózy etiologie patologie MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- štítná žláza patologie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
Follicular epithelial dysplasia (FED) is described as Hashimoto thyroiditis-related atypia and is thought to be a possible precancerous lesion. Dysplasia as an interface between normal state and carcinoma is described in a wide range of diseases and carcinogenesis chains. On the other hand, inflammation-related atypia and cancerogenesis is also widely studied. In this study, we retrospectively analyzed 91 specimens of thyroid gland surgical resections with FED during a 10-year-period at the university hospital pathology department. The study population consisted of 68 females and 15 males aged between 22 and 86 years. The preoperative cytology diagnoses had mainly been in the indeterminate categories with prevailing AUS/FLUS results in the FED-only group (p = 0.005) and suspicious for malignancy and malignant in the group with FED plus adjacent malignancy. The decision for surgery was malignancy related in 48.2% of the cases. The lesions were sized 0.1-3.5 mm and multifocal in 45.1% of the cases. Immunohistochemically, the atypical cells were cyclin D1-positive in 67.5%, galectin-3 in 72.7%, CK19 in 85.7%, and HBME-1 in 87.0% of cases. In conclusion, FED is suggested to be a pathogenetic link between inflammation-related atypia and papillary carcinoma and thus a premalignant precursor of papillary carcinoma in HT as 36.1% of the specimens contained also papillary carcinoma in the present study. Both histopathological nuclear features and the immunoprofile of FED are widely shared with that of papillary carcinoma.
Department of Biology Faculty of Medicine in Pilsen Charles University Pilsen Czech Republic
Faculty of Medicine and Health Technology Tampere University Tampere Finland
Fimlab Laboratories Tampere Finland
Pathology Department Seinäjoki Central Hospital Seinäjoki Finland
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