| Literature DB >> 12435322 |
P Gámez García1, A de Pablo Gafas, C Salas Antón, R Santolaya Cohen, L Madrigal Royo, A Varela de Ugarte.
Abstract
Dumbbell tumors are extremely rare. Most are neurogenic in origin. Growth is both inside and outside the spinal canal, and symptoms debut with medullary or spinal compression. References to non-neurogenic dumbbell tumors are uncommon. This report describes the case of a 56 year-old woman with a dumbbell angiolipoma having mediastinal and spinal cord portions. The tumor was successfully resected using a two-stage procedure. First, the spinal portion was resected using a posterior neurosurgical approach, with improvement of symptoms. Then, the mediastinal portion was removed thoracoscopically.Entities:
Mesh:
Year: 2002 PMID: 12435322 DOI: 10.1016/s0300-2896(02)75285-x
Source DB: PubMed Journal: Arch Bronconeumol ISSN: 0300-2896 Impact factor: 4.872