The New England Journal of Medicine
e-mail icon  FREE NEJM E-TOC    HOME   |   SUBSCRIBE   |   CURRENT ISSUE   |   PAST ISSUES   |   COLLECTIONS   |    Advanced Search
Sign in | Get NEJM's E-Mail Table of Contents — Free | Subscribe
 
Editorial
PreviousPrevious
Volume 331:325-327 August 4, 1994 Number 5
NextNext

Ewing's Sarcoma and the "Peanut" Tumors

Since this article has no abstract, we have provided an extract of the first 100 words of the full text and any section headings.

 Sign up for free e-toc
 

This Article
-Full Text
-Purchase this article

Tools and Services
-Add to Personal Archive
-Add to Citation Manager
-Notify a Friend
-E-mail When Cited

More Information
-PubMed Citation
The application of molecular biology to the treatment of patients with cancer took root in pediatric oncology with the landmark demonstration of the association of amplification of the N-myc oncogene with a poor prognosis in children with neuroblastoma1. Today, amplification of N-myc and the amount of DNA in tumor cells are factors that can determine the intensity of therapy for neuroblastoma. Neuroblastoma belongs to a family of primitive small-round-cell tumors, which often cause diagnostic difficulties because of their homogeneous appearance on light microscopy and their frequent lack of organ specificity. Any of these tumors can be hidden in the . . . [Full Text of this Article]

References


This article has been cited by other articles:



HOME  |  SUBSCRIBE  |  SEARCH  |  CURRENT ISSUE  |  PAST ISSUES  |  COLLECTIONS  |  PRIVACY  |  HELP  |  beta.nejm.org

Comments and questions? Please contact us.

The New England Journal of Medicine is owned, published, and copyrighted © 2008 Massachusetts Medical Society. All rights reserved.