Skip to main content

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)