Neurofibrosarcoma: Difference between revisions

Latest revision as of 18:21, 1 December 2015

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-__NOTOC__
+#REDIRECT[[Malignant peripheral nerve sheath tumor]]
-{{Infobox_Disease |
-  Name           = {{PAGENAME}} |
-  Image          = |
-  Caption        = |
-  DiseasesDB     = 32055 |
-  ICD10          = |
-  ICD9           = |
-  ICDO           = 9540/3 |
-  OMIM           = |
-  MedlinePlus    = |
-  eMedicineSubj  = |
-  eMedicineTopic = |
-  MeshID         = D018319 |
-}}
-{{SI}}
-{{CMG}}
-==Overview==
-'''Neurofibrosarcoma''' is a type of tumor combining characteristics of [[neurofibroma]] and [[fibrosarcoma]].
-It is a rare tumor type, with a relatively poor prognosis.<ref name="pmid12632346">{{cite journal |author=Neville H, Corpron C, Blakely ML, Andrassy R |title=Pediatric neurofibrosarcoma |journal=J. Pediatr. Surg. |volume=38 |issue=3 |pages=343-6; discussion 343-6 |year=2003 |pmid=12632346 |doi=10.1053/jpsu.2003.50105}}</ref>
-==References==
-{{Reflist|2}}
-{{Nervous tissue tumors }}
-[[category:Disease]]
-[[Category:Oncology]]
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