eISSN: 1897-4317
ISSN: 1895-5770
Gastroenterology Review/Przegląd Gastroenterologiczny
Current issue Archive Manuscripts accepted About the journal Editorial board Abstracting and indexing Subscription Contact Instructions for authors Ethical standards and procedures
SCImago Journal & Country Rank
3/2016
vol. 11
 
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abstract:
Letter to the Editor

A giant non-functioning pancreatic neuroendocrine carcinoma founded as an incidentaloma successfully treated with pancreatoduodenectomy

Jacek Paszkowski
,
Adam Bobkiewicz
,
Józef Świrkowicz
,
Łukasz Krokowicz
,
Jan Majewski
,
Tomasz Banasiewicz
,
Michał Drews

Gastroenterology Rev 2016; 11 (3): 211–213
Online publish date: 2016/08/05
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Pancreatic neuroendocrine tumours (PTENs) are a heterogeneous group of tumours that develop from neuroendocrine cells of the pancreas [1]. Pancreatic neuroendocrine tumours comprise a rare group of pancreatic tumours and represent about 1–2% of all tumours developing within this organ [2]. The potential of neuroendocrine cells to produce and secrete peptides and/or biogenic amines affecting the clinical presentation of the disease thus determines their division into functioning and non-functioning pancreatic neuroendocrine tumours (functioning, F-PTEN and non-functioning, NF-PTEN). General accessibility of cross-sectional imaging of the abdomen has caused a significantly increasing rate of incidentally revealed non-functioning pancreatic neuroendocrine tumours in recent years. The group of NF-PTEN represents the majority of neuroendocrine tumours of the pancreas and is estimated at 60–90% [3]. An asymptomatic pattern of the disease associated with a lack of the peptide and/or biogenic amine productions means that these tumours may present with considerable size at the time of clinical diagnosis.
We present a giant non-functioning neuroendocrine tumour of the pancreas successfully treated surgically. Surgical treatment remains the treatment of choice in this group of patients. Long-term results of surgical treatment are superior to those found in exocrine pancreatic surgery. The overall survival rate is nearly 90% in 5-year follow-up [4, 5].
A 72-year-old male was admitted to the hospital because of a tumour of the pancreas. Three months prior to the hospital admission an ultrasound scan had been performed regarding asymptomatic abdominal pain of unknown aetiology. The examination had demonstrated a tumour in the head of the pancreas about 11.5 cm in size. Besides the intermittent nonspecific abdominal pain, patient did not complain of any other disturbances. He suffered from hypertension and chronic obstructive pulmonary disease (COPD) as comorbidities. The patient’s past medical history was notable for cholecystectomy and pneumonia a year previously. On admission, his general condition was good. He did not complain of any problems. According to a physical examination, a palpable mass in the epigastric region was revealed. The patient denied weight loss, elevated temperature, jaundice, or problems with bowel movements. Diagnostics were implemented. An abdominal computed tomography (CT) scan and endocrine evaluation was provided. Imaging...


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