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Pancreatic Neuroendocrine Tumor Presenting with Carcinoid Syndrome: Case Report

Maja Berković
Vanja Zjačić-Rotkvić
Vesna Goldoni
Davor Hrabar
Nikola Karapandža


Puni tekst: engleski pdf 112 Kb

str. 347-350

preuzimanja: 1.093

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Sažetak

Carcinoid is the most common neuroendocrine tumor. It is primarily localized in the ileum and the appendix, whereas other localizations are rare. Only a small number of the carcinoids present with carcinoid syndrome (flushing, diarrhea), usually after tumor has already metastasized. A case of carcinoid tumor of uncommon localization is reported. A 54-year-old male patient presented for evaluation because of weight loss, flushing and diarrhea. Laboratory value of 5-HIAA was 775.5 mmol/l (normal values up to 72.8) and the pancreatic tumor marker CA 19-9 was increased. Ultrasonographic and magnetic resonance find-Rings localized the tumor in the prepapillary pancreatic region and visualized the spread to the liver. The diagnosis was confirmed by pathohistologic evaluation of a liver biopsy specimen. The patient was treated with Sandostatin (octreotide analog), which led to significant relief of the symptoms, although control 5-HIAA values were not reduced.

Ključne riječi

Neuroendocrine tumors, diagnosis; Pancreatic neoplasms, diagnosis; Pancreatic neoplasms, drug therapy; Carcinoid tumor, diagnosis; Carcinoid tumor, drug therapy; Case report

Hrčak ID:

14700

URI

https://hrcak.srce.hr/14700

Datum izdavanja:

1.12.2003.

Podaci na drugim jezicima: hrvatski

Posjeta: 5.778 *