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. Author manuscript; available in PMC: 2017 Sep 1.
Published in final edited form as: Clin Endocrinol (Oxf). 2016 Jun 30;85(3):400–407. doi: 10.1111/cen.13119

Table 1.

Clinicopathologic characteristics of PNETs (n=55) and non-PNETs patients (n=58).

Clinicopathologic characteristic Classification PNETs Non-PNETs
Sex, n (%) Male 34 (61.8) 25 (43.1)
Female 21 (38.2) 33 (56.9)
Criteria for MEN1, n (%) Clinical 14 (25.5) 10 (17.2)
Genetic 24 (41.4)
Genetic with one manifestation 5 (9.0) 17 (29.3)
Genetic with two manifestation 36 (65.5) 7 (12.1)
Median age (years) at diagnosis (range) 41 (18–76) 36 (15–74)*
Other NETs status, n (%) Yes 5 (9.1) 1 (1.7)
No 50 (90.9) 57 (98.3)
Tumor functional status, n (%) Functioning 18 (32.7)
Non-functioning 37 (67.3)
Tumor location, n (%) Pancreatic head and neck 7 (14.3)
Pancreatic body and tail 42 (85.7)
Tumor number, n (%) 1 20 (37.0)
2 9 (16.7)
3 4 (7.4)
4 3 (5.6)
5 3 (5.6)
>5 15 (27.7)
Median tumor size, cm (range) 1.5 (0.5–10)
Operation status, n (%) Surgery 28 (50.9)
No surgery 27 (49.1)
Lymph node metastases, n (%) Yes 7 (30.4)
No 16 (69.6)
Lymphovascular invasion, n (%) Yes 5 (17.9)
No 23 (82.1)
Distant metastases, n (%) Yes 5 (9.1)
No 50 (90.9)
AJCC staging, n (%) I 15 (53.6)
II 13 (46.4)
Vital status at last follow-up, n (%) Alive 48 (87.3)
Deceased 7 (12.7)

PNETs=pancreatic neuroendocrine tumors; MEN1=multiple endocrine neoplasia type 1; NETs=neuroendocrine tumors; AJCC=American Joint Committee on Cancer.

*

Age of patients when diagnosed with non-PNETs using most recent abdominal imaging.