| Literature DB >> 30341705 |
Christian A Koch1,2,3,4, S Petersenn5.
Abstract
Neuroendocrine neoplasms (NEN) are rare and heterogeneous. Therefore, they often remain unrecognized for many years, causing significant disease burden. We here report on four unusual NEN presentations including a metastatic NEN of the kidney, hypoglycemia caused by an insulin-like growth factor-2-oma (previously called non-islet-cell tumor hypoglycemia), multifocal pheochromocytoma in von Hippel Lindau syndrome, and ileal NEN metastatic to the heart. One could say that each one of these tumors were "black swans" and learning about them will increase further awareness of the spectrum of NEN.Entities:
Keywords: Carcinoid; Heart; Hypoglycemia; Insulin-like growth factor 2; Kidney; Neuroendocrine tumor; Pheochromocytoma; von Hippel Lindau
Mesh:
Year: 2018 PMID: 30341705 DOI: 10.1007/s11154-018-9473-0
Source DB: PubMed Journal: Rev Endocr Metab Disord ISSN: 1389-9155 Impact factor: 6.514