Difference between revisions of "IgG4-related systemic diseases"
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*[[Inflammatory pseudotumour]].<ref name=pmid18609677/> | *[[Inflammatory pseudotumour]].<ref name=pmid18609677/> | ||
*[[Sclerosing cholangitis]].<ref name=pmid18609677/> | *[[Sclerosing cholangitis]].<ref name=pmid18609677/> | ||
*[[Autoimmune pancreatitis]] (lymphoplasmacytic sclerosing pancreatitis). | |||
*Others. | *Others. | ||
Revision as of 16:26, 4 May 2012
IgG4-related systemic disease, also IgG4-related disease, is a disease characterized IgG4 positive plasma cells and fibrosis.[1]
There are several IgG4-related diseases:
- Lymphoplasmacytic sclerosing pancreatitis - a type of autoimmune pancreatitis.
- Retroperitoneal fibrosis.[2]
- Riedel's thyroiditis.
- Inflammatory pseudotumour.[2]
- Sclerosing cholangitis.[2]
- Autoimmune pancreatitis (lymphoplasmacytic sclerosing pancreatitis).
- Others.
References
- ↑ Khosroshahi, A.; Stone, JH. (Jan 2011). "A clinical overview of IgG4-related systemic disease.". Curr Opin Rheumatol 23 (1): 57-66. doi:10.1097/BOR.0b013e3283418057. PMID 21124086.
- ↑ 2.0 2.1 2.2 Kamisawa, T.; Okamoto, A. (Jul 2008). "IgG4-related sclerosing disease.". World J Gastroenterol 14 (25): 3948-55. PMID 18609677.