All issues > Volume 39(4); 1996
- Case Report
- J Korean Pediatr Soc. 1996;39(4):562-566. Published online April 15, 1996.
- Isolated Splenic Infarction in a Girl with Systemic Lupus Erythematosus
- Kyung Ran KR Park1, Hee Eun HE Lee1, Yun Ae YA Jeon1, Il Soo IS Ha1, Hae Il HI Cheong1, Joong Gon JG Kim1, Yong Y Choi1
- 1Department of Pediatrics, College of Medicine, Seoul National University, Seoul, Korea
- Abstract
- Splenic infarction is a rare disease and usually detected as a complication of SBE, atrial fibrillation, hemoglobinopathy, or myeloproliperative disorders. Although thrombotic event, such as deep vein, cerebral or renal thrombosis, is a frequent complication of SLE, there have been only a couple of cases documenting splenic infarction complicated in SLE. This is, to our knowledge, the first case report describing isolated splenic infarction in pediatric SLE. The splenic infarction
was diagnosed on abdominal CT, 99mTc-RBC splenic scan, and abdominal USG, and resolved with anticoagulant therapy. And we discussed about the possibility of antiphospholipid syndrome as a cause of the infarction in this case.
Keywords :Splenic infarction, Pediatric SLE, Antiphospholipid syndrome