Neurofibroma classification: Difference between revisions
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* Most common | * Most common | ||
* These are [[skin]] [[tumors]] | * These are [[skin]] [[tumors]] | ||
* Painless | |||
* Slowly growing | |||
* < 5cm diameter | |||
* Mostly solitary and sporadic, not associated with NF1 | |||
|- | |- | ||
| style="background:#DCDCDC;" align="center" + |[[Subcutaneous]] | | style="background:#DCDCDC;" align="center" + |[[Subcutaneous]] | ||
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* Uncommon | * Uncommon | ||
* Squishy | * Squishy | ||
* | * Poorly defined | ||
* Runs through the full [[skin]] thickness | |||
* Infiltrative lesions in subcutaneous fat (mostly seen in children and young adults) | |||
* Edges are difficult to define | * Edges are difficult to define | ||
* Solitary lesions and not related to any inherited condition | |||
|- | |- | ||
| style="background:#DCDCDC;" align="center" + |[[Intramuscular]] | | style="background:#DCDCDC;" align="center" + |[[Intramuscular]] | ||
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* Sometimes can occur in chains and are [[Plexiform neurofibroma|plexiform neurofibromas]] | * Sometimes can occur in chains and are [[Plexiform neurofibroma|plexiform neurofibromas]] | ||
|- | |- | ||
| style="background:#DCDCDC;" align="center" + |[[Plexiform neurofibroma|Plexiform]] | | style="background:#DCDCDC;" align="center" + |[[Plexiform neurofibroma|Plexiform]]/Intraneural | ||
| | | | ||
* | * Associated with NF1 | ||
* Diffuse involvement along a (large) nerve and its branches | |||
* Have more [[connective tissue]] that separates the [[nerve fibers]] | * Have more [[connective tissue]] that separates the [[nerve fibers]] | ||
* Gross enlargement of the nerve with nodular tumor development results in the gross pathologic appearance referred to as “bag of worms” | |||
* Generally believed to be present at [[birth]] | * Generally believed to be present at [[birth]] | ||
* Disfiguring | |||
* Affects function due to sheer size as well as neurovascular compromise | |||
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Revision as of 15:12, 26 March 2019
Neurofibroma Microchapters |
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Neurofibroma classification On the Web |
American Roentgen Ray Society Images of Neurofibroma classification |
Risk calculators and risk factors for Neurofibroma classification |
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
Neurofibroma may be classified into 5 subtypes: cutaneous/dermal/localized, subcutaneous, diffuse, intramuscular, and plexiform neurofibroma. Plexiform neurofibromas may be further sub-classified into diffuse and nodular plexiform.
Classification
Neurofibroma may be classified into following 5 subtypes:[1][2]
Types of neurofibromas | Characteristics/Description |
---|---|
Cutaneous/Dermal/Localized (90%) | |
Subcutaneous |
|
Diffuse |
|
Intramuscular |
|
Plexiform/Intraneural |
|
Plexiform neurofibromas can be further subclassified into following:[3]
Types of neurofibromas | Characteristics/Description |
---|---|
Diffuse Plexiform | |
Nodular Plexiform |
References
- ↑ Neurofibroma. Libre Pathology 2015. http://librepathology.org/wiki/index.php/Neurofibroma#cite_note-pmid15486243-2 Accessed on November 17, 2015
- ↑ https://www.nfmidwest.org/
- ↑ https://www.nfmidwest.org/