Background Gastroenteropancreatic neuroendocrine tumors (GEP-NETs) are a heterogeneous group of rare neoplasms that arise from neuroendocrine cells within the gastrointestinal tract and pancreas. They are categorized by anatomical origin foregut, midgut, and hindgut as well as tumor grade (G1–G3). Most GEP-NETs express somatostatin receptors (SSTRs
Pancytopenia, a rare presentation of hyperthyroidism
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