Classic and Follicular Variant of Papillary Thyroid Microcarcinoma: 2 Different Phenotypes Beyond Tumor Size

Author:

Sparano Clotilde1ORCID,Rotondi Mario2ORCID,Verdiani Valentina1,Brunori Paolo3,Castiglione Francesca4,Bartoli Caterina4,Perigli Giuliano5,Badii Benedetta5,Vezzosi Vania4,Simontacchi Gabriele6,Livi Lorenzo7,Antonuzzo Lorenzo8,Maggi Mario1,Petrone Luisa9ORCID

Affiliation:

1. Endocrinology Unit, Department of Experimental and Clinical Biomedical Sciences ‘Mario Serio’, University of Florence , Florence , Italy

2. Istituti Clinici Scientifici Maugeri IRCCS, Unit of Internal Medicine and Endocrinology, Department of Internal Medicine and Therapeutics, University of Pavia , Pavia , Italy

3. International Inequality Institute, London School of Economics , London , UK

4. Department of Histopathology and Molecular Diagnostics, Careggi Hospital , Florence , Italy

5. Unit of General and Endocrine Surgery, Centre of Oncological and Minimally Invasive Surgery, Department of Surgery and Translational Medicine, University of Florence , Florence , Italy

6. Radiation Oncology Unit, Careggi Hospital , Florence , Italy

7. Radiation Oncology Unit, Department of Biomedical, Experimental and Clinical Sciences “Mario Serio”, University of Florence , Florence , Italy

8. Clinical Oncology Unit, Department of Experimental and Clinical Medicine, University of Florence , Florence , Italy

9. Endocrinology Unit, Medical-Geriatric Department, Careggi Hospital , Florence , Italy

Abstract

Abstract Context Despite the wide revision of current guidelines, the management of papillary thyroid microcarcinoma (mPTC) still has to be decided case by case. There is conflicting evidence about the role of more frequent histological subtypes, and no data about potential differences at presentation. Objective Our aim was to compare the phenotype of the 2 most frequent mPTC variants, namely, classical papillary thyroid microcarcinoma (mPTCc) and the follicular variant of papillary thyroid microcarcinoma (mFVPTC) . Methods Retrospective observational study, from January 2008 to December 2017 of a consecutive series of patients with mPTCc and mFVPTC. All cases were classified according to the 2015 American Thyroid Association (ATA) risk classification. Clinical and preclinical features of mPTCc and mFVPTC at diagnosis were collected. The comparison was also performed according to the incidental/nonincidental diagnosis and differences were verified by binary logistic analysis. Results In total, 235 patients were eligible for the analysis (125 and 110 mPTCc and mFVPTC, respectively). Compared with mPTCc, mFVPTCs were more often incidental and significantly smaller (4 vs 7 mm) (P < .001 all), possibly influenced by the higher rate of incidental detection. mFVPTC and incidental (P < .001 both) tumors were significantly more often allocated within the low-risk class. A logistic regression model, with ATA risk class as the dependent variable, showed that both mFVPTC (OR 0.465 [0.235-0.922]; P = .028]) and incidental diagnosis (OR 0.074 [0.036-0.163]; P < .001) independently predicted ATA risk stratification. Conclusion mFVPTC shows some differences in diagnostic presentation compared with mPTCc, and seems to retain a significant number of favorable features, including a prevalent onset as incidental diagnosis.

Publisher

The Endocrine Society

Subject

Endocrinology, Diabetes and Metabolism

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