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Table 1 Clinical features of FPTC patients

From: Lack of germline A339V mutation in thyroid transcription factor-1 (TITF-1/NKX2.1) gene in familial papillary thyroid cancer

  Patients (n = 63)
Age at diagnosis (yr)  
   Mean ± SD 46 ± 15.5
   Range 15-78
Sex  
   No. of females (%) 47 (74.6)
   No. of males (%) 16 (25.4)
Histotype  
   No. of papillary (%) 47 (74.6)
   No. of papillary follicular variant (%) 15 (23.8)
   No. of papillary warthin-like (%) 1 (1.6)
TNM  
   No. of T1-T3 N0 M0(%) 40 (63.5)
   No. of T1-T3 N1 M0 (%) 13 (20.6)
   No. of T1-T3 N0-N1 M1 (%) 1 (1.6)
   No. of T4 N0-N1 M0 (%) 3 (4.7)
   Not available 6 (9.6)
Outcome  
   Remission (%) 45 (71.4)
   Persistent disease (%) 12 (19.1)
   Not evaluated (%) 6 (9.5)