Summary:
Introduction: Somatostatinoma is a rare, slowly growing tumor with malignity potential, most commonly located in the pancreas or
duodenum. By the time its diagnosis is established, it is usually large and liver metastases are present. Increased concentrations of somatostatin,
produced by pancreatic D cells or by intestinal mucosa, inihibit secretion of a number of GIT hormones, endocrine and exocrine
pancreatic secretion. The clinical findings include symptoms of diabetes, dyspepsia, diarrhoea, steatorhoea, abdominal pain, hypochlorhydria,
anemia. Sometimes, the finding is accidental.
A case review: The authors present a case of somatostatinoma, detected accidentaly in a 72- year- old male. The tumor originated from
the pancreatic head, partially spreading invasively into surrounding organs (duodenum), invading blood vessels and metastazing into peripancreatic
lymphonodes. The tumor was asymptomatic and was detected as an accidental finding on ultrasound and CT abdominal examinations
for the patient’s urological disorder (vesicolithiasis)
Pylorus saving hemipancreatoduodenectomy was performed and, on microscopic and subsequent immunohistochemical examination
of the resecate, a well- differentiated endocrine, somatostatin- producing pancreatic carcinoma was verified.
Key words:
malignant somatostatinoma – accidental detection of the tumor – hemipancreatoduodenectomy – verification by a pathologist
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