Poorly Differentiated Thyroid Carcinomas: How Much Poorly Differentiated is Needed?

被引:56
作者
Dettmer, Matthias [1 ,2 ]
Schmitt, Anja [2 ]
Steinert, Hans [3 ]
Haldemann, Andreas [5 ]
Meili, Andreas [7 ]
Moch, Holger [4 ]
Komminoth, Paul [6 ]
Perren, Aurel [2 ]
机构
[1] Univ Pittsburgh, Dept Pathol & Lab Med, Pittsburgh, PA 15261 USA
[2] Univ Bern, Inst Pathol, CH-3012 Bern, Switzerland
[3] Univ Zurich Hosp, Div Nucl Med, Zurich, Switzerland
[4] Univ Zurich Hosp, Inst Surg Pathol, Zurich, Switzerland
[5] Triemli Municipal Hosp, Div Nucl Med, Zurich, Switzerland
[6] Triemli Municipal Hosp, Inst Surg Pathol, Zurich, Switzerland
[7] Kantonsspital Winterthur, Div Nucl Med, Winterthur, Switzerland
关键词
thyroid; carcinoma; poorly differentiated; classification; prognosis; INSULAR COMPONENT; FOLLICULAR CARCINOMAS; PROGNOSTIC-FACTORS; SOLID PATTERNS; TURIN PROPOSAL; PAPILLARY; GLAND; EXPRESSION; MUTATIONS; FEATURES;
D O I
10.1097/PAS.0b013e31822cf962
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Background: Poorly differentiated (PD) carcinomas of the thyroid are conceptually situated between well-differentiated (papillary or follicular) carcinomas and anaplastic thyroid carcinomas. Although the morphologic criteria for PD tumors are well defined, it is not clear how much of a PD area besides a well-differentiated component in a given tumor is required to allow such a diagnosis. Methods: We identified 42 patients suffering from thyroid carcinoma with an adverse clinical outcome. Fifty patients with follicular carcinoma were added as controls. We analyzed poorly differentiated areas by applying the Turin criteria of PD carcinomas. These criteria consisted of the presence of a solid/trabecular/insular growth pattern, lack of nuclear features of papillary carcinoma, and presence of 1 of the following features: (1) convoluted nuclei, (2) tumor necrosis, (3) 3 or more mitoses per 10 high-power fields. Results: Using a cutoff value of 10% of PD areas per examined tumor surface, we identified a total of 35 PD carcinomas. Despite using a threshold of 10% of the tumor area as poorly differentiated, the survival data in a Kaplan-Meier analysis were significantly worse than those in the control group (P < 0.001) and did not differ from tumors with a PD area > 50%. In a multivariate analysis that included age, sex, tumor stage, and PD area > 10% against survival data, the only consistent significant factor was PD differentiation (P < 0.001). Conclusions: As even slight amounts of PD areas (>= 10%) in a thyroid carcinoma affect the prognosis significantly, the presence of such areas may be worth reporting in thyroid carcinomas.
引用
收藏
页码:1866 / 1872
页数:7
相关论文
共 34 条
[1]   Poorly differentiated thyroid carcinoma - It is important [J].
Akslen, LA ;
LiVolsi, VA .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2000, 24 (02) :310-311
[2]   Where to set the threshold between well differentiated and poorly differentiated follicular carcinomas of the thyroid [J].
Albores-Saavedra, J ;
Carrick, K .
ENDOCRINE PATHOLOGY, 2004, 15 (04) :297-305
[3]  
AlboresSaavedra J, 1997, CANCER, V80, P1110, DOI 10.1002/(SICI)1097-0142(19970915)80:6<1110::AID-CNCR14>3.0.CO
[4]  
2-B
[5]  
[Anonymous], 2004, WHO CLASSIFICATION T
[6]  
ASHFAQ R, 1994, CANCER, V73, P416, DOI 10.1002/1097-0142(19940115)73:2<416::AID-CNCR2820730229>3.0.CO
[7]  
2-O
[8]   Poorly differentiated carcinoma of the thyroid: validation of the Turin proposal and analysis of IMP3 expression [J].
Asioli, Sofia ;
Erickson, Lori A. ;
Righi, Alberto ;
Jin, Long ;
Volante, Marco ;
Jenkins, Sarah ;
Papotti, Mauro ;
Bussolati, Gianni ;
Lloyd, Ricardo V. .
MODERN PATHOLOGY, 2010, 23 (09) :1269-1278
[9]   N-ras mutation in poorly differentiated thyroid carcinomas:: Correlation with bone metastases and inverse correlation to thyroglobulin expression [J].
Basolo, F ;
Pisaturo, F ;
Pollina, LE ;
Fontanini, G ;
Elisei, R ;
Molinaro, E ;
Iacconi, P ;
Miccoli, P ;
Pacini, F .
THYROID, 2000, 10 (01) :19-23
[10]   POORLY DIFFERENTIATED (INSULAR) THYROID-CARCINOMA - A REINTERPRETATION OF LANGHANS WUCHERNDE STRUMA [J].
CARCANGIU, ML ;
ZAMPI, G ;
ROSAI, J .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1984, 8 (09) :655-668