Dermatofibroma classification: Difference between revisions

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{{familytree | | | | | | | | | A01 | | | | | | | | |A01=Histopathology varient of dermatofibroma}}
{{familytree | | | | | | | | | A01 | | | | | | | | |A01=[[Histopathology]] varient of dermatofibroma}}
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{{familytree | | B01 | | | | | B02 | | | | | B03 |B01=Variants that are prominent in architectural (low-power) properties|B02=Variants that are prominent in [[Cytological|cytologic]] or [[stromal]] (high-power) properties|B03=Variants that have architectural (low) and [[cytological]] or [[stromal]] (high-power) properties}}
{{familytree | | B01 | | | | | B02 | | | | | B03 |B01=Variants that are prominent in architectural (low-power) properties|B02=Variants that are prominent in [[Cytological|cytologic]] or [[stromal]] (high-power) properties|B03=Variants that have architectural (low) and [[cytological]] or [[stromal]] (high-power) properties}}
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{{familytree | | C01 | | | | | C02 | | | | | C03 |C01=1. Deep penetrating dermatofibroma
{{familytree | | C01 | | | | | C02 | | | | | C03 |C01=1. Deep penetrating dermatofibroma
2. [[Atrophic]] dermatofibroma
2. [[Atrophic]] dermatofibroma


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3. [[Myofibroblast|Myofibroblastic]] dermatofibroma  
3. [[Myofibroblast|Myofibroblastic]] dermatofibroma  


4. [[Sclerotic fibroma|Sclerotic]] dermatofibroma  
4. [[Sclerotic fibroma|Sclerotic]] dermatofibroma  
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7. Hemosiderrhotic dermatofibroma  
7. Hemosiderrhotic dermatofibroma  


8. Cholesterotic/lipidized dermatofibroma   
8. Cholesterotic/lipidized dermatofibroma   
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10. Ossifying dermatofibroma
10. Ossifying dermatofibroma


11. [[Pseudolymphoma|Pseudolymphomatous]] dermatofibroma  
11. [[Pseudolymphoma|Pseudolymphomatous]] dermatofibroma  


 
12. Dermatofibroma  with [[diffuse]] [[eosinophilic]] [[Infiltration (medical)|infiltrate]]|C03=1. Epithelioid cell histiocytoma  
12. Dermatofibroma  with [[diffuse]] [[eosinophilic]]
 
[[Infiltration (medical)|infiltrate]]|C03=1. Epithelioid cell histiocytoma  


2. Cellular benign fibrous histiocytoma  
2. Cellular benign fibrous histiocytoma  

Revision as of 17:53, 14 August 2019

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-in-Chief: Homa Najafi, M.D.[2]

Overview

There is no established system for the classification of [disease name].


Dermatofibroma may be classified according to [classification method] into [number] subtypes/groups: [group1], [group2], [group3], and [group4].


[Disease name] may be classified into [large number > 6] subtypes based on [classification method 1], [classification method 2], and [classification method 3]. [Disease name] may be classified into several subtypes based on [classification method 1], [classification method 2], and [classification method 3].


Based on the duration of symptoms, [disease name] may be classified as either acute or chronic.


If the staging system involves specific and characteristic findings and features: According to the [staging system + reference], there are [number] stages of [malignancy name] based on the [finding1], [finding2], and [finding3]. Each stage is assigned a [letter/number1] and a [letter/number2] that designate the [feature1] and [feature2].


The staging of [malignancy name] is based on the [staging system].



1. Epithelioid cell histiocytoma

2. Cellular benign fibrous histiocytoma

3. Smooth muscle proliferation in dermatofibroma

4. Multinucleate cell angiohistiocytoma

5. Cellular neurothekeoma

6. Combined DF


Classification

Dermatofibroma may be classified according to histopathology into three subtypes:

  • Variants that are prominent in architectural (low-power) properties
  • Variants that are prominent in cytologic or stromal (high-power) properties
  • Variants that have architectural (low) and cytological or stromal (high-power) properties


 
 
 
 
 
 
 
 
Histopathology varient of dermatofibroma
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Variants that are prominent in architectural (low-power) properties
 
 
 
 
Variants that are prominent in cytologic or stromal (high-power) properties
 
 
 
 
Variants that have architectural (low) and cytological or stromal (high-power) properties
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1. Deep penetrating dermatofibroma

2. Atrophic dermatofibroma

3. Aneurysmal fibrous histiocytoma

4. Haemangiopericytoma-like fibrous histiocytoma

5. Palisading cutaneous fibrous histiocytoma

6. Lichenoid, erosive, & ulcerated dermatofibroma

7. Plaque-like dermal fibromatosis, dermatofibroma
 
 
 
 
1. Clear cell dermatofibroma

2. Granular cell dermatofibroma

3. Myofibroblastic dermatofibroma

4. Sclerotic dermatofibroma

5. Keloidal dermatofibroma

6. Atypical/pseudosarcomatous fibrous histiocytoma, dermatofibroma with monster cells

7. Hemosiderrhotic dermatofibroma

8. Cholesterotic/lipidized dermatofibroma

9. Myxoid dermatofibroma

10. Ossifying dermatofibroma

11. Pseudolymphomatous dermatofibroma

12. Dermatofibroma with diffuse eosinophilic infiltrate
 
 
 
 
1. Epithelioid cell histiocytoma

2. Cellular benign fibrous histiocytoma

3. Smooth muscle proliferation in dermatofibroma

4. Multinucleate cell angiohistiocytoma

5. Cellular neurothekeoma

6. Combined DF

References