Neurofibroma natural history, complications and prognosis: Difference between revisions
Sara Mohsin (talk | contribs) |
Sara Mohsin (talk | contribs) |
||
| Line 6: | Line 6: | ||
==Natural History== | ==Natural History== | ||
* If left untreated, 10% of [[patients]] with [[plexiform neurofibroma]]s may progress to develop [[malignant peripheral nerve sheath tumor]] ([[MPNST]]) | * If left untreated, 10% of [[patients]] with [[plexiform neurofibroma]]s may progress to develop [[malignant peripheral nerve sheath tumor]] ([[MPNST]])<ref name="pmid12898075">{{cite journal |author=Mautner VF, Friedrich RE, von Deimling A, Hagel C, Korf B, Knöfel MT, Wenzel R, Fünsterer C. |title=Malignant peripheral nerve sheath tumours in neurofibromatosis type 1: MRI supports the diagnosis of malignant plexiform neurofibroma. |journal=American Journal of Pathology |volume=45 |issue=9 |pages=618–25 |year=2003 |pmid=12898075 |doi=10.1007/s00234-003-0964-6}}</ref> | ||
==Complications== | ==Complications== | ||
| Line 14: | Line 14: | ||
==Prognosis== | ==Prognosis== | ||
* [[Prognosis]] of [[neurofibroma]] is generally excellent | * [[Prognosis]] of [[neurofibroma]] is generally excellent | ||
==References== | ==References== | ||
Revision as of 18:21, 30 April 2019
|
Neurofibroma Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
Neurofibroma natural history, complications and prognosis On the Web |
|
American Roentgen Ray Society Images of Neurofibroma natural history, complications and prognosis |
|
FDA on Neurofibroma natural history, complications and prognosis |
|
CDC on Neurofibroma natural history, complications and prognosis |
|
Neurofibroma natural history, complications and prognosis in the news |
|
Blogs on Neurofibroma natural history, complications and prognosis |
|
Risk calculators and risk factors for Neurofibroma natural history, complications and prognosis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sara Mohsin, M.D.[2] Shanshan Cen, M.D. [3]
Overview
Prognosis of neurofibroma is generally excellent. If left untreated, 10% of patients with plexiform neurofibromas may progress to develop malignant peripheral nerve sheath tumor (MPNST). Local recurrence occurs rarely.
Natural History
- If left untreated, 10% of patients with plexiform neurofibromas may progress to develop malignant peripheral nerve sheath tumor (MPNST)[1]
Complications
Important complications associated with neurofibroma include:[1]
Prognosis
- Prognosis of neurofibroma is generally excellent
References
- ↑ 1.0 1.1 Mautner VF, Friedrich RE, von Deimling A, Hagel C, Korf B, Knöfel MT, Wenzel R, Fünsterer C. (2003). "Malignant peripheral nerve sheath tumours in neurofibromatosis type 1: MRI supports the diagnosis of malignant plexiform neurofibroma". American Journal of Pathology. 45 (9): 618–25. doi:10.1007/s00234-003-0964-6. PMID 12898075.