Are there specific cytologic features that can predict BRAFV600E mutational status of papillary thyroid carcinoma in fine‐needle aspiration specimens?

Author:

Mendes Juliann M.1,Elsheikh Tarik M.1ORCID,Di Marco Jessica1,Russell Jennifer1,Gladkaya Tatyana1,Nicolas Marlo M.1,Clapacs Elisha1,Bena James F.2ORCID,McAfee John L.1ORCID,Policarpio‐Nicolas Maria Luisa C.1ORCID

Affiliation:

1. Department of Pathology and Laboratory Medicine Cleveland Clinic Cleveland Ohio USA

2. Department of Quantitative Health Sciences Cleveland Clinic Cleveland Ohio USA

Abstract

AbstractBackgroundBRAFV600E mutation is the most common molecular alteration found in papillary thyroid carcinoma (PTC) and has been linked to recurrent disease or possibly more aggressive behavior. Some studies have reported sickle‐shaped nuclei (SSN) and plump pink cells (PPC) to be predictive markers of BRAF mutation in FNA cytology. We aimed to evaluate the reproducibility of the aforementioned cytologic features.MethodsA computerized search for diagnosed PTC surgical pathology cases tested for BRAFV600E mutation by Sanger DNA sequencing was performed. Blinded to BRAF results, the corresponding cytology was reviewed for presence of SSN and PPC. Classic nuclear PTC (CNPTC) features, cystic change, and psammoma bodies were also evaluated. The results were correlated with BRAFV600E mutational status and histologic subtypes.ResultsStudy cohort consisted of 113 cases (74 BRAFV600E mutated, 39 BRAFV600E wild type).SSN and combined CNPTC /SSN had positive predictive value of 74% and 75%, respectively. CNPTC showed 92% sensitivity and 20% specificity. Psammoma bodies had 92% specificity and 5% sensitivity. The presence of combined PPC/SSN showed 80% specificity, 27% sensitivity, and diagnostic accuracy of 45%. CNPTC was seen in 60/61 (98%) SSN and 45/45 (100%) PPC. There was no significant statistical association between SSN, PPC, and CNPTC with specific histologic subtypes and BRAF mutational status.ConclusionCNPTC is sensitive but not specific for BRAF mutational status. SSN, PPC, and CNPTC are not predictive markers for the presence of BRAF mutation or histologic subtypes. Additional studies may be needed to further corroborate these findings.

Funder

Cleveland Clinic

Publisher

Wiley

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