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2007 | 79 | 2 | 129-133

Article title

Somatostatinoma of the Pancreas; Difficulties in Preoperative Diagnostic Approaches - A Case Report

Content

Title variants

Languages of publication

EN

Abstracts

EN
Somatostatinoma is the rarest neuroendocrine tumor of the digestive tract. About 60% of somatostatinomas arise in the pancreas. This study presents a case of a 51-year-old male patient with tumor of the pancreas. Despite wide preoperative diagnostic examinations, it was impossible to determine the histological type of the tumor preoperatively. The patient was qualified for surgical procedure, during which the tumor was enucleated. The tumor was classified as somatostatinoma through immunohistochemical examination. The postoperative course was complicated by a small fluid collection, which arose in area of enucleation; the cistern was absorbed spontaneously. Currently, the patient is under surgical ambulatory care and is in general, in good condition.

Year

Volume

79

Issue

2

Pages

129-133

Physical description

Dates

published
1 - 2 - 2007
online
24 - 9 - 2007

Contributors

  • Department of Digestive Tract Surgery, Silesian Medical University, Katowice
  • Department of Digestive Tract Surgery, Silesian Medical University, Katowice
author
  • Department of Digestive Tract Surgery, Silesian Medical University, Katowice

References

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  • House MG, Yeo CJ, Schulick RD: Periampullary pancreatic somatostatinoma. Ann Surg Oncol 2002; 9: 869-74.[Crossref][PubMed]
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  • Soga J, Yakuwa Y: Somatostatinoma inhibitory syndrome:a statistical evaluation of 173 reported cases as compared to other pancreatic endocrino-mas. J Exp Clin Cancer Res 1999; 18: 13-22.
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  • Kaltsas GA, Besser GM, Grossman AB: Diagnosis and medical management of advanced neuroendocrine tumors. Endocr Rev 2004; 25: 458-511.[Crossref][PubMed]
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  • Becherer A, Szabo M, Karanikas G et al.: Imaging of advanced neuroendocrine tumors with 18F-FDOPA PET. J Nucl Med 2004; 45: 1161-67.
  • Norton JA, Cromack DT, Shawker TH: Intraoperative ultrasonographic localization of islet cell tumors. A prospective comparison to palpation. Ann Surg 1988; 207: 160-68.[PubMed][Crossref]
  • Ramage JK, Davies AHG, Ardill J et al.: Guidelines for the management of gastroenteropancreatic neuroendocrine (including carcinoid) tumours. Gut 2005; 54: 1-16.[WoS]
  • Plöckinger U, Wiedenmann B: Diagnosis of non-functioning neuro-endocrine gastro-enteropancreatic tumours. Neuroendocrinology 2004; 80: 35-38.[Crossref][PubMed]
  • Brentjens R, Saltz L: Islet cell tumors of the pancreas: the medical oncologist's perspective. Surg Clin North Am 2001; 81: 527-542.[Crossref]
  • Cichocki A: Chirurgiczne leczenie guzów neuroendokrynnych przewodu pokarmowego. Onkologia po Dyplomie. Wydanie specjalne. 2005; 42-46.
  • Madeira I, Terris B, Voss M et al.: Prognostic factor in patients with endocrine tumors of the duodenopancreatic area. Gut 1998; 43: 422-27.[Crossref]

Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.-psjd-doi-10_2478_v10035-007-0021-y
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