Neurofibrosarcoma

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Neurofibrosarcoma
Classification and external resources
ICD-O: 9540/3
DiseasesDB 32055
MeSH D018319

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Neurofibrosarcoma

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Overview

Neurofibrosarcoma is a type of tumor combining characteristics of neurofibroma and fibrosarcoma.

It is a rare tumor type, with a relatively poor prognosis.[1]

References

  1. Neville H, Corpron C, Blakely ML, Andrassy R (2003). "Pediatric neurofibrosarcoma". J. Pediatr. Surg. 38 (3): 343-6; discussion 343-6. doi:10.1053/jpsu.2003.50105. PMID 12632346.



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Acknowledgement and Attribution Regarding Sources of Content

Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

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