Mast cell tumor pathophysiology: Difference between revisions
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*Mediator release from mast cells has a central role in the development of type 1 hypersensitivity. | *Mediator release from mast cells has a central role in the development of type 1 hypersensitivity. | ||
*In systemic mastocytosis, abnormal proliferation and microscopic infiltration of mast cells involves skin, [[bone marrow]], [[gastrointestinal tract]], [[liver]], and [[spleen]]. | *In systemic mastocytosis, abnormal proliferation and microscopic infiltration of mast cells involves skin, [[bone marrow]], [[gastrointestinal tract]], [[liver]], and [[spleen]]. | ||
*It is thought that the effects of mastocytosis relate at least in part to mediator release | *It is thought that the effects of mastocytosis relate at least in part to mediator release. | ||
==References== | ==References== | ||
Revision as of 15:28, 29 February 2016
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Pathophysiology
- A mast cell originates from the bone marrow and is normally found throughout the connective tissue of the body.
- It is a normal component of the immune system and as it releases histamine it is associated with allergic reactions.
- Mast cell granules contain histamine, heparin, platelet-activating factor, and other substances.[1]
- Mediator release from mast cells has a central role in the development of type 1 hypersensitivity.
- In systemic mastocytosis, abnormal proliferation and microscopic infiltration of mast cells involves skin, bone marrow, gastrointestinal tract, liver, and spleen.
- It is thought that the effects of mastocytosis relate at least in part to mediator release.
References
- ↑ Brière C (2002). "Use of a reverse saphenous skin flap for the excision of a grade II mast cell tumor on the hind limb of a dog". Can Vet J. 43 (8): 620–2. PMID 12170840.