» Articles » PMID: 19953247

Re-evaluation of Histopathological Factors Affecting Prognosis of Differentiated Thyroid Carcinoma in an Iodine-sufficient Country

Overview
Journal World J Surg
Publisher Wiley
Specialty General Surgery
Date 2009 Dec 3
PMID 19953247
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Poorly differentiated thyroid carcinoma (PDTC) was recognized as an independent clinicohistological entity of thyroid cancer in the 2004 World Health Organization (WHO) classifications, separated from papillary (PTC) and follicular carcinoma (FTC). The Turin proposal provides more specific criteria for the diagnosis of PDTC. However, in an iodine-sufficient country such as Japan, PDTC comprises <1% of all thyroid cancers. In 1983, Sakamoto analyzed pathological characteristics of PTC and FTC that recurred within 5 years after initial surgery and identified solid, trabecular, insular (STI) and scirrhous growth patterns as important predictors of poor prognosis. We re-evaluated the impact of histopathological findings on the clinical course of PTC and FTC.

Materials And Methods: Specimens from 376 consecutive cases diagnosed as PTC (n = 351) or FTC (n = 25) between 1994 and 2001 were reviewed.

Results: Nine (2%) patients were diagnosed with PDTC according to WHO criteria. Only 1 case (0.3%) met the Turin criteria. In addition, STI components were seen in various specimens as follows: >or=50%, >or=10% but <50%, >0% but <10%, and 0% of specimens for 9 (2%), 31 (8%), 19 (5%), and 317 cases (85%), respectively. As for cause-specific survival, a significant difference was apparent between the >or=50% and >or=10% but <50% groups. Disease-free survival was identical between these groups and was significantly worse than in the >0% but <10% and 0% groups. According to multivariate analysis, histological features of STI >or=10% and squamous metaplasia were significantly related to cause-specific survival, but scirrhous infiltration, necrosis, nuclear atypia, and vascular invasion were not. The presence of STI at a level >or=10% was also a significant risk factor, together with clinical risk factors including large tumor size, large nodal metastasis, and distant metastasis. According to AMES risk-group definition, clinically high-risk patients with STI >or=10% showed the worst 10-year cause-specific survival, at 57%, irrespective of total thyroidectomy with radioactive iodine (RAI) treatment. Ten of 25 PTC patients (40%) with STI >or=10% developed cervical recurrence, whereas 9 of 15 FTC patients (60%) with STI >or=10% showed distant metastasis.

Conclusions: The measurement of STI >or=10% represents a distinctly important risk factor for patient survival. In particular, clinically high-risk patients with STI >or=10% need further therapy beyond RAI. Original histological pattern, as papillary or follicular, affects the site of recurrence.

Citing Articles

Prevalence of Differentiated High-Grade Thyroid Carcinoma Among Well-Differentiated Tumors: A Systematic Review and Meta-Analysis.

Poma A, Macerola E, Ghossein R, Tallini G, Basolo F Thyroid. 2023; 34(3):314-323.

PMID: 38115626 PMC: 10951568. DOI: 10.1089/thy.2023.0350.


Clinicopathological Characteristics and Recurrence-Free Survival of Rare Variants of Papillary Thyroid Carcinomas in Korea: A Retrospective Study.

Kim M, Cho S, Park Y, Ahn H, Kim H, Suh Y Endocrinol Metab (Seoul). 2021; 36(3):619-627.

PMID: 34107674 PMC: 8258331. DOI: 10.3803/EnM.2021.974.


Prognostic Impact of the Turin Criteria in Poorly Differentiated Thyroid Carcinoma.

Akaishi J, Kondo T, Sugino K, Ogimi Y, Masaki C, Hames K World J Surg. 2019; 43(9):2235-2244.

PMID: 31098668 DOI: 10.1007/s00268-019-05028-5.


The impact of microscopic extrathyroid extension on outcome in patients with clinical T1 and T2 well-differentiated thyroid cancer.

Nixon I, Ganly I, Patel S, Palmer F, Whitcher M, Tuttle R Surgery. 2011; 150(6):1242-9.

PMID: 22136847 PMC: 4151609. DOI: 10.1016/j.surg.2011.09.007.


Prognostic factors of papillary and follicular carcinomas in Japan based on data of kuma hospital.

Ito Y, Miyauchi A J Thyroid Res. 2011; 2012:973497.

PMID: 21977332 PMC: 3184434. DOI: 10.1155/2012/973497.

References
1.
NISHIYAMA R . Another dissertation on poorly differentiated carcinomas: is it really necessary?. Adv Anat Pathol. 1999; 6(5):281-6. DOI: 10.1097/00125480-199909000-00004. View

2.
Hiltzik D, Carlson D, Tuttle R, Chuai S, Ishill N, Shaha A . Poorly differentiated thyroid carcinomas defined on the basis of mitosis and necrosis: a clinicopathologic study of 58 patients. Cancer. 2006; 106(6):1286-95. DOI: 10.1002/cncr.21739. View

3.
Hay I, Bergstralh E, Goellner J, Ebersold J, Grant C . Predicting outcome in papillary thyroid carcinoma: development of a reliable prognostic scoring system in a cohort of 1779 patients surgically treated at one institution during 1940 through 1989. Surgery. 1993; 114(6):1050-7; discussion 1057-8. View

4.
Sugitani I, Fujimoto Y, Yamada K, Yamamoto N . Prospective outcomes of selective lymph node dissection for papillary thyroid carcinoma based on preoperative ultrasonography. World J Surg. 2008; 32(11):2494-502. DOI: 10.1007/s00268-008-9711-9. View

5.
Akslen L, Livolsi V . Poorly differentiated thyroid carcinoma--it is important. Am J Surg Pathol. 2000; 24(2):310-3. DOI: 10.1097/00000478-200002000-00030. View