Neurofibroma natural history, complications and prognosis: Difference between revisions
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==Complications== | ==Complications== | ||
* [[Malignant transformation|Malignant transformation (plexiform neurofibroma)]] | * Complications that can develop as a result of neurofibroma include the following:<ref name="pmid12898075" /> | ||
* [[Local]] [[Recurrence plot|recurrence]] ([[rare]]) | **[[Malignant transformation|Malignant transformation (plexiform neurofibroma)]] | ||
**[[Local]] [[Recurrence plot|recurrence]] ([[rare]]) | |||
==Prognosis== | ==Prognosis== | ||
Latest revision as of 18:33, 4 November 2019
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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
- Complications that can develop as a result of neurofibroma include the following:[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.