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incomplete data. TNM information was retrieved by the following codes: Derived AJCC Stage Group 7th ed (2010+), Derived AJCC Stage Group 6th ed (2004+), CS tumor size (2004+), Regional nodes positive (1988+). Collected information included recode of race
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- value Age (years) 55.0 (46–68.5) 59.5 (46–68) 0.8679 Gender (male/female) 10/26 (27.8/72.2) 15/35 (30.0/70.0) 0.8228 Tumor size (mm) 29 (18–36) 17 (14–24) 0.0002 Intact PTH level (pg/mL) 246.5 (160
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Yes 1.197 (1.034–1.410) 0.016 Nodular goiter No 1 Yes 0.839 (0.732–0.962) 0.012 a Tumor size, maximum meridian of tumor. Logistic regression model As shown in Table 4 , male sex
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tumor size ranged from 4 to 19 cm (median: 9.7, IQR: 7–12). The genetic analysis was available for 12 cases of MEN2A; eight had mutation in codon 634, and one each in codon 618, 531, 709, and 804 of RET proto-oncogene. The most common site for metastasis
Department of General Surgery, Sir Run-Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China
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Department of General Surgery, Sir Run-Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China
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Department of General Surgery, Sir Run-Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China
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Department of General Surgery, Sir Run-Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China
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Department of General Surgery, Sir Run-Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China
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, time at diagnosis), clinicopathological characteristics (tumor size, grade, SEER stage, lymph node metastasis, tumor metastasis), and therapy information (gallbladder surgery, lymph node surgery) were extracted from the SEER database. The original data
Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden
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Department of Breast and Endocrine Surgery, Karolinska University Hospital, Stockholm, Sweden
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Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden
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-morbidities, blood pressure, biochemistry, imaging and tumor size recorded in the files were noted. Patients with relapse of their pheochromocytoma were included only for the first episode. High-performance liquid chromatography (HPLC) was used for determinations
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compared to somatic RET mutations ( 7 , 9 ). We previously demonstrated that the presence of a somatic RET p.Met918Thr mutation correlated with larger tumor size while it was significantly lower in tumors smaller than 2 cm ( 12 ). We hypothesized
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only added after alpha-blockade was applied. Fluid intake was encouraged. Patients with hypertension or a larger tumor size were treated by i.v. crystalloid and colloid fluid (2000 mL/day) or blood transfusion at 2–3 days before surgery. The criteria
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papillary thyroid carcinomas (CPTC). However, they have not been defined as a subtype of PTC, and their clinical characteristics have not been fully investigated. The tumor size of PTC is important in clinical management and is used as an indicator for
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such as male sex, advanced age, tumor size, extrathyroidal extension of the neoplasm, and incomplete surgical resection can negatively affect the prognosis ( 9 ). An important aspect of understanding neoplastic aggressiveness is the assessment of the