Impact of reclassifying noninvasive follicular variant of papillary thyroid carcinoma on the risk of malignancy in The Bethesda System for Reporting Thyroid Cytopathology.
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Faquin WC
Massachusetts General Hospital, Boston, Massachusetts.
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Wong LQ
Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania.
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Afrogheh AH
Massachusetts General Hospital, Boston, Massachusetts.
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Ali SZ
Johns Hopkins Hospital, Baltimore, Maryland.
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Bishop JA
Johns Hopkins Hospital, Baltimore, Maryland.
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Bongiovanni M
Institute of Pathology, University Hospital, Lausanne, Switzerland.
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Pusztaszeri MP
Geneva University Hospitals, Geneva, Switzerland.
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VandenBussche CJ
Johns Hopkins Hospital, Baltimore, Maryland.
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Gourmaud J
Institute of Pathology, University Hospital, Lausanne, Switzerland.
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Vaickus LJ
Massachusetts General Hospital, Boston, Massachusetts.
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Baloch ZW
Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania.
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Published in:
- Cancer cytopathology. - 2016
English
BACKGROUND
Recent discussions have focused on redefining noninvasive follicular variant of papillary thyroid carcinoma (NI-FVPTC) as a neoplasm rather than a carcinoma. This study assesses the potential impact of such a reclassification on the implied risk of malignancy (ROM) for the diagnostic categories of The Bethesda System for Reporting Thyroid Cytopathology (TBSRTC).
METHODS
The study consisted of consecutive fine-needle aspiration biopsy (FNAB) cases collected between January 1, 2013 and June 30, 2014 from 5 academic institutions. Demographic information, cytology diagnoses, and surgical pathology follow-up were recorded. The ROM was calculated with and without NI-FVPTC and was presented as a range: all cases (ie, overall risk of malignancy [OROM]) versus those with surgical follow-up only.
RESULTS
The FNAB cohort consisted of 6943 thyroid nodules representing 5179 women and 1409 men with an average age of 54 years (range, 9-94 years). The combined average ROM and OROM for the diagnostic categories of TBSRTC were as follows: nondiagnostic, 4.4% to 25.3%; benign, 0.9% to 9.3%; atypia of undetermined significance/follicular lesion of undetermined significance (AUS/FLUS), 12.1% to 31.2%; follicular neoplasm (FN), 21.8% to 33.2%; suspicious for malignancy (SM), 62.1% to 82.6%; and malignant, 75.9% to 99.1%. The impact of reclassifying NI-FVPTC on the ROM and OROM was most pronounced and statistically significant in the 3 indeterminate categories: the AUS/FLUS category had a decrease of 5.2% to 13.6%, the FN category had a decrease of 9.9% to 15.1%, and the SM category had a decrease of 17.6% to 23.4% (P < .05), whereas the benign and malignant categories had decreases of 0.3% to 3.5% and 2.5% to 3.3%, respectfully. The trend of the effect on the ROM and OROM was similar for all 5 institutions.
CONCLUSIONS
The results from this multi-institutional cohort indicate that the reclassification of NI-FVPTC will have a significant impact on the ROM for the 3 indeterminate categories of TBSRTC.
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bronze
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Persistent URL
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https://folia.unifr.ch/global/documents/249755
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