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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: 696* citiraj
APA 6th Edition
Berković, M., Zjačić-Rotkvić, V., Goldoni, V., Hrabar, D. i Karapandža, N. (2003). Pancreatic Neuroendocrine Tumor Presenting with Carcinoid Syndrome: Case Report. Acta clinica Croatica, 42 (4), 347-350. Preuzeto s https://hrcak.srce.hr/14700
MLA 8th Edition
Berković, Maja, et al. "Pancreatic Neuroendocrine Tumor Presenting with Carcinoid Syndrome: Case Report." Acta clinica Croatica, vol. 42, br. 4, 2003, str. 347-350. https://hrcak.srce.hr/14700. Citirano 27.01.2020.
Chicago 17th Edition
Berković, Maja, Vanja Zjačić-Rotkvić, Vesna Goldoni, Davor Hrabar i Nikola Karapandža. "Pancreatic Neuroendocrine Tumor Presenting with Carcinoid Syndrome: Case Report." Acta clinica Croatica 42, br. 4 (2003): 347-350. https://hrcak.srce.hr/14700
Harvard
Berković, M., et al. (2003). 'Pancreatic Neuroendocrine Tumor Presenting with Carcinoid Syndrome: Case Report', Acta clinica Croatica, 42(4), str. 347-350. Preuzeto s: https://hrcak.srce.hr/14700 (Datum pristupa: 27.01.2020.)
Vancouver
Berković M, Zjačić-Rotkvić V, Goldoni V, Hrabar D, Karapandža N. Pancreatic Neuroendocrine Tumor Presenting with Carcinoid Syndrome: Case Report. Acta clinica Croatica [Internet]. 2003 [pristupljeno 27.01.2020.];42(4):347-350. Dostupno na: https://hrcak.srce.hr/14700
IEEE
M. Berković, V. Zjačić-Rotkvić, V. Goldoni, D. Hrabar i N. Karapandža, "Pancreatic Neuroendocrine Tumor Presenting with Carcinoid Syndrome: Case Report", Acta clinica Croatica, vol.42, br. 4, str. 347-350, 2003. [Online]. Dostupno na: https://hrcak.srce.hr/14700. [Citirano: 27.01.2020.]

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

[hrvatski]

Posjeta: 2.947 *