Case Report
Copyright ©The Author(s) 2016.
World J Gastrointest Endosc. Feb 10, 2016; 8(3): 192-197
Published online Feb 10, 2016. doi: 10.4253/wjge.v8.i3.192
Table 1 World Health Organization classification of pancreatic neuroendocrine tumors
GradeKi-67 index (%)Mitotic count/10 HPF
G1 ≤ 2< 2
G23-202-20
G3> 20> 20
TNMSize (cm)Muscularis propria invasion
T1a< 1_
T1b1-2_
T2> 2+
Table 2 Patient demographic information and baseline characteristics of the tumours
No. of patients127
Age, yr
Mean (range)59 (27-89)
Sex, male/female10-17
No. of tumors30
Functioning19
Non functioning11
Type of functioning tumor
Insulinoma18
Vipoma1
Diameter, mm
Mean (range)12.5 (5-22)
Table 3 Procedural outcomes
No. of treatment session per tumor
Mean (range)1.43 (1-3)
Alcohol volume, mL
Mean (range)1.83 (0.18-8)
Technical success, n (%)30/30 (100)
Clinical success1, n (%)
Functioning19/19 (100)
Non functioning27/10 (70)
Adverse events3, n (%)11 (25.5)
Early (within one week), n (%)9 (21)
Pancreatic necrotic lesion1 (2.3)
Mild pancreatitis7 (16.2)
Abdominal pain1 (2.3)
Late, n (%)2 (4.6)
Hematoma and ulceration of the duodenal wall1 (2.3)
Main pancreatic duct stricture1 (2.3)
Follow-up, mo
Mean (range)13.4 (2-38)