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CLC number: R73

On-line Access: 2010-01-01

Received: 2009-06-12

Revision Accepted: 2009-10-13

Crosschecked: 2009-12-02

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Journal of Zhejiang University SCIENCE B 2010 Vol.11 No.1 P.22-26

http://doi.org/10.1631/jzus.B0900166


Pancreatic somatostatinoma with obscure inhibitory syndrome and mixed pathological pattern


Author(s):  Bo ZHANG, Qiu-ping XIE, Shun-liang GAO, Yan-biao FU, Yu-lian WU

Affiliation(s):  Department of Surgery, the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310009, China; more

Corresponding email(s):   wuyulian@medmail.com.cn

Key Words:  Neuroendocrine tumor, Somatostatinoma, Somatostatinoma syndrome, Pancreatic hormone-producing tumor, Pancreatectomy


Bo ZHANG, Qiu-ping XIE, Shun-liang GAO, Yan-biao FU, Yu-lian WU. Pancreatic somatostatinoma with obscure inhibitory syndrome and mixed pathological pattern[J]. Journal of Zhejiang University Science B, 2010, 11(1): 22-26.

@article{title="Pancreatic somatostatinoma with obscure inhibitory syndrome and mixed pathological pattern",
author="Bo ZHANG, Qiu-ping XIE, Shun-liang GAO, Yan-biao FU, Yu-lian WU",
journal="Journal of Zhejiang University Science B",
volume="11",
number="1",
pages="22-26",
year="2010",
publisher="Zhejiang University Press & Springer",
doi="10.1631/jzus.B0900166"
}

%0 Journal Article
%T Pancreatic somatostatinoma with obscure inhibitory syndrome and mixed pathological pattern
%A Bo ZHANG
%A Qiu-ping XIE
%A Shun-liang GAO
%A Yan-biao FU
%A Yu-lian WU
%J Journal of Zhejiang University SCIENCE B
%V 11
%N 1
%P 22-26
%@ 1673-1581
%D 2010
%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.B0900166

TY - JOUR
T1 - Pancreatic somatostatinoma with obscure inhibitory syndrome and mixed pathological pattern
A1 - Bo ZHANG
A1 - Qiu-ping XIE
A1 - Shun-liang GAO
A1 - Yan-biao FU
A1 - Yu-lian WU
J0 - Journal of Zhejiang University Science B
VL - 11
IS - 1
SP - 22
EP - 26
%@ 1673-1581
Y1 - 2010
PB - Zhejiang University Press & Springer
ER -
DOI - 10.1631/jzus.B0900166


Abstract: 
somatostatinoma is a very rare neuroendocrine tumor that originates from D cells and accounts for less than 1% of all gastrointestinal endocrine tumors. The duodenum is the most frequent site for this tumor, followed by the pancreas. We here describe a 46-year-old Chinese woman who developed pancreatic somatostatinoma presenting with the characteristic “inhibitory” syndrome, but the symptoms were obscure and seemingly uncorrelated. This case is also unique for its large tumor size and mixed pathological pattern. Distal pancreatectomy was performed, and the patient has remained well since operation. As the syndromes of somatostatinoma may be obscure and atypical, clinicians should review all clinical findings to obtain an accurate diagnosis. Aggressive surgery is preferred to improve the survival.

Darkslateblue:Affiliate; Royal Blue:Author; Turquoise:Article

Reference

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