| Literature DB >> 10962331 |
J R Leavitt1, D L Harold, R B Robinson.
Abstract
A 67-year-old woman was evaluated for asymptomatic microscopic hematuria. Intravenous urography and computed tomography demonstrated an adrenal mass, but the workup for a functional adrenal tumor was negative. The mass was surgically resected, with a histologic diagnosis of adrenal ganglioneuroma. No further treatment was necessary. After the diagnosis was made, the patient reported a family history positive for neuroblastic tumors. Two of her grandchildren had presented at early ages with a ganglioneuroblastoma and a third had presented with a ganglioneuroma. This presentation is unique because ganglioneuroma, especially that of adrenal origin, is rare in the adult population, and familial cases are extremely uncommon.Entities:
Mesh:
Year: 2000 PMID: 10962331 DOI: 10.1016/s0090-4295(00)00695-6
Source DB: PubMed Journal: Urology ISSN: 0090-4295 Impact factor: 2.649