만성 특발혈소판감소자반병 환아에서 발생한 전신홍반루프스

Title
만성 특발혈소판감소자반병 환아에서 발생한 전신홍반루프스
Other Titles
Systemic Lupus Erythematosus That Developed in a Child with Chronic Idiopathic Thrombocytopenic Purpura
Author(s)
신동훈김기홍최종수김영식[김영식]
Keywords
Childhood; Idiopathic thrombocytopenic purpura; Systemic lupus erythematosus
Issue Date
201011
Publisher
대한피부과학회
Citation
대한피부과학회지, v.48, no.11, pp.1024 - 1026
Abstract
Idiopathic thrombocytopenic purpura (ITP) is a common bleeding disorder in children and it is caused by autoantibodies against platelet surface antigens. Systemic lupus erythematosus (SLE) is a chronic autoimmune disease that can affect any part of the body and so result in diverse clinical and laboratory manifestations, including thrombocytopenia. It is known that only 10∼15% of all SLE cases are diagnosed during childhood. Thrombocytopenia may be the sole manifestation early in the course of SLE, whereas SLE can subsequently develop in 1∼5% of ITP patients. We report here on an interesting case of SLE that developed in an eleven year-old girl with chronic and refractory ITP and who underwent splenectomy.
URI
http://hdl.handle.net/YU.REPOSITORY/23324
ISSN
0494-4739
Appears in Collections:
의과대학 > 피부과학교실 > Articles
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