Intravenous Immunoglobulin-Induced Hemolytic Anemia in a Patient With Juvenile Dermatomyositis

被引：0
|
作者：
Clemenz, Melanie R. [1 ]
McGowan, Joseph Wilson [1 ]
Shuler, Marshall J. [1 ]
Lynn, Annette W. [1 ]
机构：
[1] Univ S Carolina, Sch Med, Columbia, SC 29208 USA
来源：
JOURNAL OF DRUGS IN DERMATOLOGY | 2013年 / 12卷 / 01期
关键词：
IMMUNE THROMBOCYTOPENIC PURPURA; GUILLAIN-BARRE-SYNDROME; COMPLEMENT; GLOBULIN; THERAPY; EFFICACY; DISEASES;
D O I：
暂无
中图分类号：
R75 [皮肤病学与性病学];
学科分类号：
100206 ;
摘要：
We report a case of hemolytic anemia in a female patient with juvenile dermatomyositis. Rapidly progressive hemolysis developed during prednisone and azathioprine combination therapy 4 days after completing intravenous immunoglobulin (IVIG) treatment. While the blood smear revealed spherocytes and polychromasia, direct and indirect antiglobulin tests were negative. In the following case report, we propose probable IVIG-induced hemolytic anemia and explore the pathomechanisms that may account for hemolysis. J Drugs DermatoL 2013;12(1):111-113.
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页码：111 / 113
页数：3
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