Hamartoma classification: Difference between revisions
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==Overview== | ==Overview== | ||
Hamartomas may be classified into different types based on their location, such as | 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.<ref name="kumar"> Kumar V, Abbas AK, Aster JC. Robbins Basic Pathology. Elsevier Health Sciences; 2012.</ref> | ||
==Classification== | ==Classification== |
Revision as of 16:18, 26 January 2016
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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
- Heart
- Rhabdomyoma[2]
- Hypothalamus
- Hypothalamic hamartoma[2]
- Kidneys
- Angiomyolipoma[2]
- Spleen
- Splenic hamartoma[2]
Lesion class
Based on the lesion class, hamartomas can be classified into the following types:[1]
- Bone-forming tumors
- Cartilage-forming tumors
- Fiber-forming tumors
- Nonossifying fibroma
- Fibrous dysplasia
- Mazabraud syndrome
- Benign non–matrix-forming tumors
References