FNA needle rinses preserved in Cytolyt are acceptable specimen type for mutation testing of thyroid nodules

Haijun Zhou, Dina R. Mody, Debora Smith, Maura B. Lloyd, Jon Kemppainen, Jeffrey Houghton, Dennis Wylie, Anna E. Szafranska-Schwarzbach, Hidehiro Takei*

*Corresponding author for this work

Research output: Contribution to journalArticle

4 Scopus citations

Abstract

Introduction: This study investigated the application of molecular testing to residual thyroid fine-needle aspiration material from needle rinses collected in Cytolyt. Materials and methods: Two thyroid needle rinses from 135 patients were collected in Cytolyt during routine diagnostic workup in our institution. Molecular testing was performed to detect 14 genetic alterations in BRAF, K-, H-, N-RAS genes as well as RET/PTC1, RET/PTC3, and PAX8/PPARγ and verified by next generation sequencing and correlated with cytologic diagnoses. Results: Molecular testing revealed a total of 17 mutations across specimens with benign nodule (n = 5; HRAS, NRAS), Hürthle cell neoplasm (n = 2; BRAF, HRAS) and Papillary thyroid carcinoma (n = 10, 9. BRAF, 1 KRAS) cytology. No RNA gene rearrangements were detected. Conclusions: Mutations and translocations associated with thyroid cancer can be detected in thyroid fine-needle aspiration needle rinses preserved in Cytolyt specimens collected during routine patient management, which are typically discarded when a diagnosis is attained.

Original languageEnglish (US)
Pages (from-to)128-135
Number of pages8
JournalJournal of the American Society of Cytopathology
Volume4
Issue number3
DOIs
StatePublished - May 1 2015

Keywords

  • Cytolyt
  • Molecular testing
  • Thyroid fine-needle aspiration

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

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    Zhou, H., Mody, D. R., Smith, D., Lloyd, M. B., Kemppainen, J., Houghton, J., Wylie, D., Szafranska-Schwarzbach, A. E., & Takei, H. (2015). FNA needle rinses preserved in Cytolyt are acceptable specimen type for mutation testing of thyroid nodules. Journal of the American Society of Cytopathology, 4(3), 128-135. https://doi.org/10.1016/j.jasc.2015.01.001