| Literature DB >> 18663423 |
Abstract
Neuroblastomas have a very heterogenic clinical presentation, ranging from relatively benign forms with the potential of spontaneous regression, to foudroyant malignant forms. Over half of neuroblastomas must be classified as high-risk tumors with a markedly high rate of recurrence. Despite multidisciplinary therapeutic approaches, the survival rate of children with this type of tumor is still below 40%. An ever-growing amount of data from international studies dating from the early 1970s onwards, points to the necessity of re-evaluating the medical approach in establishing the diagnosis and staging, understanding tumor biology and pathology, as well as therapy planning.Entities:
Mesh:
Year: 2008 PMID: 18663423 DOI: 10.1007/s00117-008-1652-7
Source DB: PubMed Journal: Radiologe ISSN: 0033-832X Impact factor: 0.635