Influence of Tumor Number on Clinicopathologic Features and Outcomes of Patients With Papillary Thyroid Carcinoma

被引:17
作者
Feng, Jia-Wei [1 ]
Wu, Wan-Xiao [1 ]
Hu, Jun [1 ]
Hong, Li-Zhao [1 ]
Qin, An-Cheng [2 ]
Jiang, Yong [1 ]
Ye, Jing [1 ]
机构
[1] Soochow Univ, Changzhou First Peoples Hosp, Affiliated Hosp 3, Changzhou, Peoples R China
[2] Nanjing Med Univ, Suzhou Municipal Hosp, Affiliated Suzhou Hosp, Suzhou, Peoples R China
关键词
Papillary thyroid carcinoma; Papillary thyroid microcarcinoma; Multifocality; Lymph node metastasis; Recurrence-free survival; ASSOCIATION MANAGEMENT GUIDELINES; INDEPENDENT CLONAL ORIGIN; LYMPH-NODE METASTASIS; EXTRATHYROIDAL EXTENSION; PROGNOSTIC-SIGNIFICANCE; ADULT PATIENTS; CANCER; MULTIFOCALITY; RISK; SIZE;
D O I
10.1093/ajcp/aqaa102
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Objectives: The purpose of this study was to investigate the significance of tumor number on clinicopathologic factors and outcomes of patients with papillary thyroid carcinoma (PTC). Methods: We retrospectively analyzed 667 patients with PTC. We compared clinicopathologic features of patients with a different tumor number. Cox proportional hazards model was used to analyze risk factors of recurrence. Results: In papillary thyroid microcarcinoma (PTMC), the increase in the number of tumor foci was related to a higher risk of minimal extrathyroidal extension (ETE) and lymphovascular invasion (P < .05). Patients with PTMC with four or more foci had a significantly higher risk of central lymph node metastasis (CLNM) and lateral lymph node metastasis (LLNM) than patients with solitary tumors (P < .05 ). Patients with macro-PTC with four or more ,foci and with three foci had a higher risk of gross ETE and lymphovascular invasion than patients with solitary tumors (P < .05). The increase in the tumor number was related to a higher risk of CLNM in macro-PTC (P < .05). The number of foci was the independent predictor of recurrence in patients with macro-PTC (P < .05). Conclusions: An increase in the number of tumors was associated with an increased risk of aggressive clinicopathologic features in PTMC and macro-PTC. The number of tumor foci could influence risk of recurrence in macro-PTC.
引用
收藏
页码:848 / 858
页数:11
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