Neuroendocrine gastric carcinoma in a young patient

Author:

Svorcan Petar1,Alimpijevic Tamara2,Usaj Slavica3,Bojic Danijela1,Protic Marjana1,Djordjevic Jelena1,Vrinic Dusica1,Krstic Miodrag2ORCID,Dapcevic Branka1

Affiliation:

1. University Clinical Center Zvezdara, Department of Gastroenterohepatology, Belgrade%SR71-10

2. Clinical Center of Serbia, Clinic for Gastroenterohepatology, Belgrade%SR13-01.08.36

3. Institute of Oncology, Sremska Kamenica%SR23-01.05.50

Abstract

Background. Neuroendocrine tumors cover a spectrum of neoplasms showing wide variations in their clinicopathological and pathogenetic features, as well as prognosis. They may develop throughout the whole gastrointestinal tract. Case report. We described a case of gastric neuroendocrine carcinoma in a 29-year-old male. The patient presented with chronic continuous abdominal pain and weight loss over a 6- month period. Preoperative diagnosis, operative findings, histology and immunohistochemistry of the tumor confirmed the diagnosis of the rare neuroendocrine gastric carcinoma, stage T2N1. Conclusion. Case reports of this rare tumor are important, because of the paucity of studies noted in the gastrointestinal literature as a result of poor identification prior to the advent of modern immunohistochemistry. Significance of accurately diagnosing gastrointestinal neuroendocrine tumors is crucial for an appropriate treatment.

Publisher

National Library of Serbia

Subject

Pharmacology (medical),General Medicine

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