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Case Reports
. 2022 Nov 16;25(1):9.
doi: 10.3892/etm.2022.11708. eCollection 2023 Jan.

Unknown‑primary neuroendocrine neoplasms diagnosed by short‑acting somatostatin test: Case series in one institution

Affiliations
Case Reports

Unknown‑primary neuroendocrine neoplasms diagnosed by short‑acting somatostatin test: Case series in one institution

Tsung-Kun Chang et al. Exp Ther Med. .

Abstract

Neuroendocrine neoplasms (NENs) are a rare heterogeneous group of neoplasms that arise from neuroendocrine cells. Unknown-primary NENs (UP-NENs) are particularly challenging to diagnose and treat. Techniques such as immunohistochemical stains, functional imaging studies, and molecular cancer classifier assays may help clinicians identify the origin of a tumor. However, numerous medical facilities lack the necessary medical equipment, such as functional imaging scanning, to provide patients with a complete primary tumor survey. Even these tests are not enough to determine the original tumor in some cases. The present case series described the diagnosis and treatment outcomes of patients with UP-NEN in a single institution. The medical records of four patients treated between November 2012 and January 2022 were retrospectively reviewed and clinical symptoms, diagnostic methods, image findings and treatment modalities were considered. All patients were diagnosed having functional UP-NENs by using a short-acting somatostatin test. These patients were treated with long-acting release somatostatin analogs along with a positive result. Short-acting somatostatin is an alternatively simple method to determine if a patient has UP-NENs that are functional or expresses somatostatin receptors in the absence of imaging scanning.

Keywords: diagnosis; neuroendocrine neoplasms; short-acting somatostatin test; treatment; unknown-primary.

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Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Figure 1
Figure 1
Schematic diagram of short-acting somatostatin test (Day 0: Within 24 h prior to the injection of sandostatin). CgA, chromogranin A; other specific bioactive markers, bioactive markers which associated with patient's clinical symptoms, such as gastrin and insulin.

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