Neuroendocrine disorders: problems of diagnosis (clinical treatment)
https://doi.org/10.24412/2790-1289-2025-2-93-101
Abstract
The heterogeneity of neuroendocrine tumors not only in their localization, but also in their clinical manifestations, the lack of clear criteria and algorithms for their diagnosis, as well as the low alertness of doctors in the general clinical network regarding the timely detection of this group of tumors, in most cases leads to their late diagnosis, resulting in only the palliative stage of their treatment. A clinical case is presented to demonstrate the relevance of the problem.
A clinical case. Since March 2020, the patient has been periodically bothered by loose, mushy stools. During an examination in the clinic, according to computed tomography of the abdominal organs from 02/20/2021, a neoplasm of the head and body of the pancreas with invasion of the portal and splenic veins, subtotal lesion of the pancreas with vascular invasion) and multiple liver metastases was detected, taking into account the results of computed tomography studies, pancreatic malignancy, T3NxM1, multiple metastases in the liver.
Conclusions. The variety of clinical manifestations of neuroendocrine tumors complicates their early diagnosis and treatment, which requires high oncological alertness, effective interaction of specialists and the creation of national protocols for early detection and therapy.
About the Authors
S. E. YessentayevaKazakhstan
Yesentaeva Suriya Yertugyrovna – Doctor of Medical Sciences, docent, Head of the Department of Oncology, chemotherapist
Almaty
Zh. K. Zhakenova
Kazakhstan
Zhakypbekova Aidana Bagdatokyzy
Almaty
G. E. Sarsenbaeva
Kazakhstan
Sarsenbayeva Galiya Ermekovna
Almaty
E. N. Beisebayev
Kazakhstan
Beisebayev Eldar Nurlanovich – PhD.
Almaty
A. N. Baimakhasheva
Kazakhstan
Baymakhasheva Annel Niyazbekovna – Doctor of Biological Sciences
Almaty
A. S. Ozharova
Kazakhstan
Ozharova Ainel Serikbekovna – Chemotherapist, Almaty Regional Multidisciplinary Clinic
Almaty
phone: +7 775 104 46 12
References
1. Artamonova, E. V., Gorbunova, V. A., Delektorskaya, V. V., et al. (2024). Neĭroendokrinnye neoplazii zheludochno-kishechnogo trakta i podzheludochnoĭ zhelezy. Prakticheskie rekomendatsii RUSSCO. Ch. 1.1. Malignant tumors, 14(3s2), 427-444.
2. WHO Classification of Tumours Editorial Board. (2022). Endocrine and neuroendocrine tumours (5th ed., Vol. 8). Lyon: International Agency for Research on Cancer.
3. Service, F. J., Natt, N., & Thompson, G. B. (1995). Hypoglycemic disorders. New England Journal of Medicine, 332(17), 1144-1152; Wermers, R. A., Fatourechi, V., & Wynne, A. G. (2019). The glucagonoma syndrome. Endocrine Practice, 25(11), 1145-1150.
4. Reid, M. D., Bagci, P., Ohike, N., et al. (2021). Update on pancreatic somatostatinomas. Annals of Diagnostic Pathology, 51(3), 151592.
5. Cryer, P. E. (2019). Hypoglycemia-associated autonomic failure. Endocrine Reviews, 40(3), 768-798.
6. Pavel, M., O’Toole, D., Costa, F., et al. (2016). ENETS consensus: multidisciplinary management. Neuroendocrinology, 103(2), 172-185.
7. Howe, J. R., Merchant, N. B., Conrad, C., et al. (2020). North American guidelines for NET management. Pancreas, 49(1), 1-33.
8. Koumarianou, A., Daskalakis, K., Tsoli, M., Kaltsas, G., & Pavel, M. (2022). Efficacy, safety and unmet needs of evolving medical treatments for carcinoid syndrome. Journal of Neuroendocrinology, 34(7), e13174. DOI: https://doi.org/10.1111/jne.13174.
9. Aluri, V., & Dillon, J. S. (2017). Biochemical testing in neuroendocrine tumors. Endocrinology and Metabolism Clinics of North America, 46(3), 669-677.
10. Halperin, D. M., Shen, C., Dasari, A., et al. (2017). Frequency of the carcinoid syndrome at neuroendocrine tumour diagnosis: A populationbased study. The Lancet Oncology, 18(4), 525-534.
11. Shepelkevich, A. P., Krasnyĭ, S. A., Gradusha, A. V., & Luzan, A. M. (2020). Sovremennye podkhody k diagnostike i lecheniiu neĭroendokrinnykh novoobrazovaniĭ. Lechebnoe Delo, (2)72, 5-15.
12. DeVita, V. T., Lawrence, T. S., & Rosenberg, S. A. (2019). Cancer: Principles & Practice of Oncology, 11, 2429-2444.
13. Marasco, M., Romano, E., Arrivi, G., et al. (2024). Exploring carcinoid syndrome in neuroendocrine tumors: Insights from a multidisciplinary narrative review. Cancers (Basel), 16(22), 3831. DOI: https://doi.org/10.3390/cancers16223831.
14. DeVita, V. T., Norton, J. A., & Lawrence, T. S. (2019). Carcinoid tumors and the carcinoid syndrome. In Cancer: Principles & Practice of Oncology, 11, 2445-2451.
Review
For citations:
Yessentayeva S.E., Zhakenova Zh.K., Sarsenbaeva G.E., Beisebayev E.N., Baimakhasheva A.N., Ozharova A.S. Neuroendocrine disorders: problems of diagnosis (clinical treatment). Actual Problems of Theoretical and Clinical Medicine. 2025;(2):93-101. (In Kazakh) https://doi.org/10.24412/2790-1289-2025-2-93-101