| Literature DB >> 18036401 |
Barton Kenney1, Kathleen E Richkind, Gary Friedlaender, Eduardo Zambrano.
Abstract
Lipofibromatosis is a relatively rare pediatric neoplasm, which usually manifests as an ill-defined soft tissue mass involving the upper and lower distal extremities, the trunk, and, less frequently, the head. To date, no cytogenetic abnormalities have been reported in this uncommon neoplasm. We present a case of lipofibromatosis featuring a three-way t(4;9;6) translocation in a 5-year-old boy.Entities:
Mesh:
Year: 2007 PMID: 18036401 DOI: 10.1016/j.cancergencyto.2007.08.011
Source DB: PubMed Journal: Cancer Genet Cytogenet ISSN: 0165-4608