Evans syndrome and its link with systemic lupus erythematosus

Evans syndrome is a rare syndrome associated with the presence of autoimmune hemolytic anemia and simultaneous or sequential development of thrombocytopenia. It was first described by Evan and Duane in 1951. It is one of the rare presenting features of autoimmune disorders, especially systemic lupus...

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Main Authors: Satish Mendonca, Sachin Srivastava, Rajan Kapoor, Devika Gupta, Pooja Gupta, M L Sharma
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2016-01-01
Series:Saudi Journal of Kidney Diseases and Transplantation
Online Access:http://www.sjkdt.org/article.asp?issn=1319-2442;year=2016;volume=27;issue=1;spage=147;epage=149;aulast=Mendonca
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author Satish Mendonca
Sachin Srivastava
Rajan Kapoor
Devika Gupta
Pooja Gupta
M L Sharma
author_facet Satish Mendonca
Sachin Srivastava
Rajan Kapoor
Devika Gupta
Pooja Gupta
M L Sharma
author_sort Satish Mendonca
collection DOAJ
description Evans syndrome is a rare syndrome associated with the presence of autoimmune hemolytic anemia and simultaneous or sequential development of thrombocytopenia. It was first described by Evan and Duane in 1951. It is one of the rare presenting features of autoimmune disorders, especially systemic lupus erythematosus (SLE), and sometimes may even precede the onset of disease. Primary Evans syndrome with no cause is very rare and is seen in children. Here, we describe a case of secondary Evans syndrome with severe hemolytic anemia leading to acute kidney injury and recovery thereafter only to develop lupus nephritis a few months later. This is one of the rare presentations of SLE and there are only anecdotal case reports.
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spelling doaj.art-ecfb0ae57b6d4afcb256faf6b3fc24592022-12-21T19:46:08ZengWolters Kluwer Medknow PublicationsSaudi Journal of Kidney Diseases and Transplantation1319-24422016-01-0127114714910.4103/1319-2442.174177Evans syndrome and its link with systemic lupus erythematosusSatish MendoncaSachin SrivastavaRajan KapoorDevika GuptaPooja GuptaM L SharmaEvans syndrome is a rare syndrome associated with the presence of autoimmune hemolytic anemia and simultaneous or sequential development of thrombocytopenia. It was first described by Evan and Duane in 1951. It is one of the rare presenting features of autoimmune disorders, especially systemic lupus erythematosus (SLE), and sometimes may even precede the onset of disease. Primary Evans syndrome with no cause is very rare and is seen in children. Here, we describe a case of secondary Evans syndrome with severe hemolytic anemia leading to acute kidney injury and recovery thereafter only to develop lupus nephritis a few months later. This is one of the rare presentations of SLE and there are only anecdotal case reports.http://www.sjkdt.org/article.asp?issn=1319-2442;year=2016;volume=27;issue=1;spage=147;epage=149;aulast=Mendonca
spellingShingle Satish Mendonca
Sachin Srivastava
Rajan Kapoor
Devika Gupta
Pooja Gupta
M L Sharma
Evans syndrome and its link with systemic lupus erythematosus
Saudi Journal of Kidney Diseases and Transplantation
title Evans syndrome and its link with systemic lupus erythematosus
title_full Evans syndrome and its link with systemic lupus erythematosus
title_fullStr Evans syndrome and its link with systemic lupus erythematosus
title_full_unstemmed Evans syndrome and its link with systemic lupus erythematosus
title_short Evans syndrome and its link with systemic lupus erythematosus
title_sort evans syndrome and its link with systemic lupus erythematosus
url http://www.sjkdt.org/article.asp?issn=1319-2442;year=2016;volume=27;issue=1;spage=147;epage=149;aulast=Mendonca
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