Hamartoma classification: Difference between revisions
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* Hypothalamic hamartoma | * Hypothalamic hamartoma | ||
* Neurofibromatosis in von Recklinghausen disease | * Neurofibromatosis in von Recklinghausen disease | ||
* Neuroepithelial cells in tuberous sclerosis | * Neuroepithelial cells in tuberous sclerosis | ||
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*Melanocytic nevi | *Melanocytic nevi | ||
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===Lesion class=== | ===Lesion class=== |
Revision as of 16:26, 10 September 2018
Hamartoma Microchapters |
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Hamartoma classification On the Web |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Maria Fernanda Villarreal, M.D. [2]
Overview
Hamartomas may be classified into different types based on their location, such as: lung (most common), heart, hypothalamus, kidneys, or spleen. Other classifications can consider lesion class, dividing hamartomas into 4 different categories, such as: bone-forming, cartilage-forming, fiber-forming, and benign non–matrix-forming.[1]
Classification
Location
Based on the location, hamartomas can be classified into the following types:
Location | Type |
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CNS |
|
Lung |
|
Heart |
|
Kidneys |
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Spleen |
|
Skin |
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Lesion class
Based on the lesion class, hamartomas can be classified into the following types:
- Bone-forming tumors
- Cartilage-forming tumors
- Fiber-forming tumors
- Nonossifying fibroma
- Fibrous dysplasia
- Mazabraud syndrome
- Benign non–matrix-forming tumors
References
- ↑ Kumar V, Abbas AK, Aster JC. Robbins Basic Pathology. Elsevier Health Sciences; 2012.