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Title:
Zollinger-Ellisonov sindrom: prikaz primera
Authors:
ID
Krajnc, Mitja
(
Author
)
ID
Čokolič, Miro
(
Author
)
Files:
http://www.dlib.si/details/URN:NBN:SI:doc-1268XWRY
Language:
Slovenian
Work type:
Not categorized
Typology:
1.04 - Professional Article
Organization:
UM - University of Maribor
Abstract:
Izhodišča. Zollinger-Ellisonov sindrom je izjemno redka bolezen, ki je posledica čezmernega in avtonomnega izločanja gastrina iz gastrinomskih celic. Za bolezen je značilna huda in na zdravljenje odporna oblika ulkusne bolezni prebavil, ki lahko ogroža življenje bolnika. Tumor je v večini primerov maligen. Prikazan je primer 44-letnega bolnika s to boleznijo. Zaključki. Predstavljamo načela sodobne obravnave bolnika s sumom na Zollinger-Ellisonov sindrom: klinično sliko, laboratorijsko diagnostiko in preiskave za zamejitev tumorja ter osnove zdravljenja. Tumor je bil pri našem bolniku patohistološko opredeljen kot karcinoid z manjšim deležem gastrinomskih celic.
Year of publishing:
2006
Number of pages:
str. II-111 - II-115
Numbering:
Letn. 75, supl. II
PID:
20.500.12556/DKUM-55927
UDC:
616.37
ISSN on article:
1318-0347
COBISS.SI-ID:
2495807
NUK URN:
URN:SI:UM:DK:DJ4EBHSJ
Publication date in DKUM:
21.12.2015
Views:
3289
Downloads:
78
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Record is a part of a journal
Title:
Zdravniški vestnik. glasilo Slovenskega zdravniškega društva
Publisher:
Slovensko zdravniško društvo
ISSN:
1318-0347
COBISS.SI-ID:
32893696
Secondary language
Language:
English
Title:
Zollinger-Ellison syndrome: a case report
Abstract:
Background. Zollinger-Ellison syndrome is the consequence of excessive and autonomous secretion of gastrin from gastrinoma cells. The disease is exceptionally rare and characterized by severe and treatment-resistant peptic disease that can become life-threatening for a patient. In most cases, gastrinoma is malignant. A case of 44-year patient is presented. Conclusions. We present clinical manifestations, laboratory diagnostic tests, modalities of tumor localization and forms of treatment that are clinically relevant in a patient, suspected of having this rare disease. Pathohistologically, our patient's tumor was identified as a carcinoid with minor gastrinoma fraction.
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