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Unexpected Finding of a Small Intestinal Neuroendocrine Tumor: A Case Report and Literature Review

Elena Patanè, Sebastian Douglas Sgardello, Boumediene Guendil, Ian Fournier, Ziad Abbassi

(Division of Visceral Surgery, Department of Surgery, Sion Hospital, Sion, Switzerland)

Am J Case Rep 2020; 21:e917759

DOI: 10.12659/AJCR.917759


BACKGROUND: The incidence of neuroendocrine tumors (NETs) has increased in recent years. They can affect every area of the human body that presents cells with a secretory function. In this report, we focus on gastrointestinal NETs. The small bowel (SI) is the most affected area and SI-NETs have recently become more common than adenocarcinomas. Inside the small intestine, the appendix suffers from this pathology more than other organs.
CASE REPORT: Our case report deals with a 70 years-old man with extensive abdominal pain due to ingestion of an apricot kernel. A CT abdominal scan showed, around the kernel, a mechanical ileus with inflammation of the distal ileum and thickening of the intestinal wall. During the operation, we replaced laparoscopy with mini-laparotomy, performing an ileocecectomy due to suspicion of a tumor lesion. The histopathological exam revealed a well-differentiated neuroendocrine tumor (NET G1) of the distal ileum.
CONCLUSIONS: This case report shows that SI-NETs can be found in cases of small bowel occlusion. Depending on the size and distinction, such patients can have good survival rates.

This paper has been published under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) allowing to download articles and share them with others as long as they credit the authors and the publisher, but without permission to change them in any way or use them commercially.
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