Neuroendocrine tumor G3: a pancreatic well-differentiated neuroendocrine tumor with a high proliferative rate

2015 ◽  
Vol 8 (6) ◽  
pp. 414-420 ◽  
Author(s):  
Hiroki Tanaka ◽  
Shimpei Matsusaki ◽  
Youichirou Baba ◽  
Yoshiaki Isono ◽  
Hiroaki Kumazawa ◽  
...  
2020 ◽  
pp. 454-455
Author(s):  
Maria Rosaria Raspollini ◽  
Alessia Cimadamore ◽  
Rodolfo Montironi ◽  
Antonio Lopez-Beltran

2013 ◽  
Vol 8 (1) ◽  
Author(s):  
Stefano Fiori ◽  
Alessandro Del Gobbo ◽  
Gabriella Gaudioso ◽  
Lucio Caccamo ◽  
Sara Massironi ◽  
...  

2016 ◽  
Vol 66 (12) ◽  
pp. 706-707
Author(s):  
Tokiko Nakai ◽  
Tomonori Kawasaki ◽  
Takashi Tada ◽  
Motoo Ishida ◽  
Akari Iwakoshi ◽  
...  

2018 ◽  
Vol 16 (3) ◽  
pp. 496-507 ◽  
Author(s):  
Daniel Benten ◽  
Yasmin Behrang ◽  
Ludmilla Unrau ◽  
Victoria Weissmann ◽  
Gerrit Wolters-Eisfeld ◽  
...  

2020 ◽  
Vol 48 (3) ◽  
pp. 287-289
Author(s):  
Anwin Joseph Kavanal ◽  
Sanjay K. Bhadada ◽  
Ashwani Sood ◽  
Gurjeet Kaur ◽  
Amber Parwaiz ◽  
...  

2018 ◽  
Vol 06 (01) ◽  
pp. e81-e82
Author(s):  
Lucinda Tullie ◽  
Bhumita Vadgama ◽  
Ravindar Anbarasan ◽  
Michael Stanton ◽  
Henrik Steinbrecher

AbstractA 9-year-old boy, with previous anorectal malformation and neuropathic bladder and bowel, underwent ileocystoplasty, Monti–Mitrofanoff and appendix antegrade colonic enema procedure. The tip of the macroscopically normal appendix was sent for routine histopathology. Microscopy demonstrated a 5-mm well-differentiated neuroendocrine tumor extending into muscularis propria. Ki-67 index was <2%. Due to margin involvement, the appendix conduit and surrounding skin were re-excised and a tube cecostomy was created through a separate incision. Microscopy revealed no residual neuroendocrine tumor, and no further treatment was required.


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