| Literature DB >> 16921843 |
V Gimeno Argente1, M Bosquet Sanz, M A Bonillo García, L Gómez Pérez, J L Pontones Moreno, J F Jiménez Cruz.
Abstract
The existence of bilateral renal angiomyolipoma (AML) is fairly infrequent, especially when not associated with such syndromes as tuberous sclerosis or linfangioleimiomatosis. Here we present the case of a 40-year-old woman who was accidentally diagnosed at week 33rd of gestation by an ultrasound, of bilateral renal AML and that could be treated with kidney sparing conservative treatment. We have also done a review of the literature focusing on its management and its relationship with pregnancy.Entities:
Mesh:
Year: 2006 PMID: 16921843 DOI: 10.1016/s0210-4806(06)73506-9
Source DB: PubMed Journal: Actas Urol Esp ISSN: 0210-4806 Impact factor: 0.994