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PAPILLARY MICROCARCINOMA IN COMPARISON WITH LARGER PAPILLARY THYROID CARCINOMA IN BRAF(V600E) MUTATION, CLINICOPATHOLOGICAL FEATURES, AND IMMUNOHISTOCHEMICAL FINDINGS

Cited 67 time in Web of Science Cited 68 time in Scopus
Authors

Park, Young Joo; Kim, Young A.; Lee, You Jin; Kim, Soon Hui; Kim, Kyung Won; Youn, Yeo Kyu; Park, Do Joon; Cho, Bo Youn; Kim, Kwang Hyun; Chung, June Key; Park, So Yeon

Issue Date
2010-01
Publisher
JOHN WILEY & SONS INC
Citation
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK; Vol.32 1; 38-45
Keywords
papillary thyroid carcinomapapillary thyroid microcarcinomaimmunohistochemistryclinicopathological featuresBRAF mutation
Abstract
Background. Papillary thyroid microcarcinoma (PMC; <= 51 cm) is thought to take a benign course during the lifetime. However, recent studies showed high recurrence rates for PMC. Methods. We analyzed the clinicopathological features, long-term prognosis, and some molecular characteristics including BRAF(V600E) mutation by retrospectively reviewing the records of 1150 patients with papillary thyroid carcinoma (PTC), 278 with PMC, and 868 with PTC > 1 cm. Results. The prevalence of extrathyroidal invasion (52.2%) and initial nodal metastasis (34.9%) in patients with PMC was surprisingly high and almost as high as that for patients with PTC (72.4% and 51.8%, respectively). The rate of recurrent or persistent disease did not differ between patients with PMC and PTC (recurrent or persistent disease, 6.1% vs 14.1%: 53.4- vs 84.2-month follow-up; n = 98 vs 647; corrected P = .112). The frequency of BRAF(V600E) mutation was similar in patients with PMC and PTC (65.6% vs 67.2%). Immunohistochemical staining showed no different expression pattern according to the tumor size. Conclusion. These results suggest that PMC is not an occult cancer and it can act like larger PTC. Therefore, PMC should not be underestimated in practice. (C) 2009 Wiley Periodicals, Inc. Head Neck 32: 38-45, 2010
ISSN
1043-3074
Language
English
URI
https://hdl.handle.net/10371/76561
DOI
https://doi.org/10.1002/hed.21142
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