Observer variation in the diagnosis of follicular variant of papillary thyroid carcinoma

被引:376
作者
Lloyd, RV
Erickson, LA
Casey, MB
Lam, KY
Lohse, CM
Asa, SL
Chan, JKC
DeLellis, RA
Harach, R
Kakudo, K
LiVolsi, VA
Rosai, J
Sebo, TJ
Sobrinho-Simoes, M
Wenig, BM
Lae, ME
机构
[1] Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Dept Stat, Rochester, MN 55905 USA
[3] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[4] Queen Elizabeth Hosp, Dept Pathol, Kowloon, Hong Kong, Peoples R China
[5] Brown Univ, Sch Med, Dept Lab Med & Pathol, Providence, RI 02912 USA
[6] Dr A Onativia Hosp, Serv Pathol, Salta, Argentina
[7] Wakayama Med Univ, Dept Pathol, Wakayama, Japan
[8] Univ Penn, Med Ctr, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[9] Natl Tumor Inst, Dept Pathol, Milan, Italy
[10] Univ Porto, Inst Mol Pathol & Immunol, P-4100 Oporto, Portugal
[11] Beth Israel Deaconess Med Ctr, Dept Pathol & Lab Med, New York, NY 10003 USA
关键词
follicular variant of papillary carcinoma; thyroid; observer variation;
D O I
10.1097/01.pas.0000135519.34847.f6
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The histopathologic diagnosis of follicular variant of papillary thyroid carcinoma (FVPCA) can be difficult. Recent reports have suggested that this neoplasm may be frequently overdiagnosed by pathologists. We examined the observer variation in the diagnosis of FVPCA in 87 tumors by 10 experienced thyroid pathologists. The criteria that the reviewers considered most helpful for making a diagnosis of FVPCA were also assessed. A concordant diagnosis of FVPCA was made by all 10 reviewers with a cumulative frequency of 39%. In this series, 24.1% of the patients had metastatic disease (n = 21). In the cases with metastatic disease, a diagnosis of FVPCA was made by all 10 reviewers with a cumulative frequency of 66.7%, and 7 of the reviewers made a diagnosis of FVPCA with a cumulative frequency of 100%. The most important criteria used to diagnose FVPCA included the presence of cytoplasmic invaginations into the nucleus (pseudo-inclusions), abundant nuclear grooves, and ground glass nuclei. These results suggest that although the diagnosis of FVPCA is variable even among experienced thyroid pathologists, most reviewers agreed on this diagnosis for patients with metastatic disease. The use of well-defined histopathologic features should improve the consistency in diagnosing FVPCA. Since most cases with metastatic disease had obvious invasion, caution should be used in making a diagnosis of FVPCA in the absence of the major histopathologic features or clear-cut invasive growth.
引用
收藏
页码:1336 / 1340
页数:5
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    Karen, D
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