J Korean Pediatr Soc.
2002 May;45(5):664-668.
Hemophagocytic Syndrome with Kawasaki Disease and Peripheral Gangrene
- Affiliations
-
- 1Department of Pediatrics, Yonsei University, Wonju College of Medicine, Wonju, Korea. khm9120@wonju.yonsei.ac.kr
- 2Department of Clinical Pathology, Yonsei University, Wonju College of Medicine, Wonju, Korea.
Abstract
-
A twenty six months-old boy developed hemophagocytic syndrome during the course of Kawasaki disease. Despite the appropriate treatment modalities for Kawasaki disease, he developed thrombocytopenia, hepatomegaly, high-grade fever, hypertriglyceridemia, peripheral gangrene, and evidence of hemophagocytosis in bone marrow biopsy. Although the course was stormy, he responded well to a combination therapy of corticosteroid and etoposide.