Neuroendocrine tumors of the small intestine: presentation of a clinical case and literature review
Abstract
The prevalence of neuroendocrine tumors (NET) has increased over the past few decades, probably due to early diagnosis, increased alertness and widespread endoscopic and imaging studies in the diagnosis of diseases of the gastrointestinal tract (GIT). Neuroendocrine tumors that occur in the small intestine are considered rare malignancies. Despite this, both the incidence and prevalence of NET of the small intestine are gradually increasing. According to retrospective studies, the standardized incidence rate of small intestine NET was 1.46 per 100,000 populations in 2018, equaling the incidence of lung NET. To date, there are no statistics on the incidence of NET in the Russian Federation. This makes it difficult to analyze the results of treatment and to develop a diagnostic algorithm.
The work analyzes the data of newest publications on the clinical manifestations of NET of the small intestine, the main diagnostic and therapeutic methods used in this pathology and presents a clinical case of small intestine NET.
Conclusion. In the early stages of the disease, most patients have slight symptoms or none at all.
About the Authors
E. V. FedotovaRussian Federation
A. L. Petrushin
Russian Federation
M. N. Nechaeva
Russian Federation
O. A. Shangin
Russian Federation
M. Yu. Valkov
Russian Federation
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Review
For citations:
Fedotova E.V., Petrushin A.L., Nechaeva M.N., Shangin O.A., Valkov M.Yu. Neuroendocrine tumors of the small intestine: presentation of a clinical case and literature review. Bashkortostan Medical Journal. 2025;20(1):111-120. (In Russ.)