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==Overview==
 
 
==Pathogenesis==
Evans syndrome is an [[autoimmune disease]] in which an individual's [[antibodies]] attack their own [[red blood cell]]s and [[platelet]]s.<ref name="pmid14782741">{{cite journal |author=Evans RS, Takahashi K, Duane RT, Payne R, Liu C |title=Primary thrombocytopenic purpura and acquired hemolytic anemia; evidence for a common etiology |journal=A.M.AARRAYrchives of internal medicine |volume=87 |issue=1 |pages=48–65 |year=1951 |pmid=14782741 |doi=}}</ref> Both of these events may occur simultaneously or one may follow on from the other.<ref name="pmid16398647">{{cite journal |author=Norton A, Roberts I |title=Management of Evans syndrome |journal=Br. J. Haematol. |volume=132 |issue=2 |pages=125–37 |year=2006 |pmid=16398647 |doi=10.1111/j.1365-2141.2005.05809.x}}</ref>
* Its overall pathology resembles a combination of [[autoimmune hemolytic anemia]] and [[idiopathic thrombocytopenic purpura]].<ref name="pmid14782741"/> Autoimmune hemolytic anemia is a condition in which the red blood cells that normally carry [[oxygen]] and [[carbon dioxide]] are destroyed by an autoimmune process. Idiopathic thrombocytopenic purpura is a condition in which platelets are destroyed by an autoimmune process. Platelets are a component of blood that contribute to the formation of [[blood clot]]s in the body to prevent bleeding.
==Genetics==
 
==Associated Conditions==
 
==Gross Pathology==
 
==Microscopic Pathology==


==References==
==References==

Revision as of 17:27, 10 January 2016

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Overview

Pathogenesis

Evans syndrome is an autoimmune disease in which an individual's antibodies attack their own red blood cells and platelets.[1] Both of these events may occur simultaneously or one may follow on from the other.[2]

  • Its overall pathology resembles a combination of autoimmune hemolytic anemia and idiopathic thrombocytopenic purpura.[1] Autoimmune hemolytic anemia is a condition in which the red blood cells that normally carry oxygen and carbon dioxide are destroyed by an autoimmune process. Idiopathic thrombocytopenic purpura is a condition in which platelets are destroyed by an autoimmune process. Platelets are a component of blood that contribute to the formation of blood clots in the body to prevent bleeding.

Genetics

Associated Conditions

Gross Pathology

Microscopic Pathology

References

  1. 1.0 1.1 Evans RS, Takahashi K, Duane RT, Payne R, Liu C (1951). "Primary thrombocytopenic purpura and acquired hemolytic anemia; evidence for a common etiology". A.M.AARRAYrchives of internal medicine. 87 (1): 48–65. PMID 14782741.
  2. Norton A, Roberts I (2006). "Management of Evans syndrome". Br. J. Haematol. 132 (2): 125–37. doi:10.1111/j.1365-2141.2005.05809.x. PMID 16398647.