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.

Keyword

Etoposide; Hemophagocytic syndrome; Bone marrow biopsy; Kawasaki disease; Peripheral gangrene

MeSH Terms

Biopsy
Bone Marrow
Etoposide
Fever
Gangrene*
Hepatomegaly
Humans
Hypertriglyceridemia
Lymphohistiocytosis, Hemophagocytic*
Male
Mucocutaneous Lymph Node Syndrome*
Thrombocytopenia
Etoposide
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