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
* Run through the full [[skin]] thickness
* 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
|
|
* Usually present on large [[nerves]]
* 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
|}
|}



Revision as of 15:12, 26 March 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

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%)
  • Most common
  • These are skin tumors
  • Painless
  • Slowly growing
  • < 5cm diameter
  • Mostly solitary and sporadic, not associated with NF1
Subcutaneous
Diffuse
  • Uncommon
  • 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
  • Solitary lesions and not related to any inherited condition
Intramuscular
Plexiform/Intraneural
  • Associated with NF1
  • Diffuse involvement along a (large) nerve and its branches
  • 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
  • Disfiguring
  • Affects function due to sheer size as well as neurovascular compromise

Plexiform neurofibromas can be further subclassified into following:[3]

Types of neurofibromas Characteristics/Description
Diffuse Plexiform
Nodular Plexiform

References


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