| Literature DB >> 17922161 |
Gernot Rott1, Martin Biggemann, Martin Pfohl.
Abstract
Insulinomas are rare, mostly benign neuroendocrine tumors, originating in 99% of cases from the pancreas, that synthesize and secrete insulin, causing symptomatic hypoglycemia. Today the treatment of choice is surgical removal. We present the case of an 84-year-old woman with a symptomatic insulinoma who refused surgery and was treated with arterial embolization using trisacryl gelatin microspheres as definitive treatment.Entities:
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Year: 2007 PMID: 17922161 DOI: 10.1007/s00270-007-9185-4
Source DB: PubMed Journal: Cardiovasc Intervent Radiol ISSN: 0174-1551 Impact factor: 2.740