Macrophage Activation Syndrome in a Child with Systemic Juvenile Rheumatoid Arthritis
Journal of Korean Medical Science
;
: 695-698, 2005.
Artigo
em Inglês
| WPRIM
| ID: wpr-25771
ABSTRACT
Macrophage activation syndrome (MAS) is a rare and potentially fatal complication of rheumatic disorders in children. We describe a 13-month-old boy in whom MAS developed as a complication of systemic juvenile rheumatoid arthritis (S-JRA). He suffered from fever and generalized rash followed by multiple joints swelling for four months before admission. Physical examination revealed cervical lymphadenopathy and hepatosplenomegaly. Laboratory findings were abnormal liver enzymes, increased triglyceride and ferritin levels, coagulopathies resembling disseminated intravascular coagulation, anemia and thrombocytopenia. Hyperplasia of hemophagocytic macrophages was remarkable in his bone marrow. Methylprednisolone and cyclosporin therapy resulted in clinical and laboratory improvements. This is the third case of MAS associated with S-JRA in Koreans, and the first one, in which hemophagocytic macrophages were proven in bone marrow.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Tempo de Tromboplastina Parcial
/
Artrite Juvenil
/
Tempo de Protrombina
/
Aspartato Aminotransferases
/
Esplenomegalia
/
Síndrome
/
Contagem de Células Sanguíneas
/
Antígenos de Diferenciação Mielomonocítica
/
Antígenos CD
/
Alanina Transaminase
Limite:
Humanos
/
Lactente
/
Masculino
Idioma:
Inglês
Revista:
Journal of Korean Medical Science
Ano de publicação:
2005
Tipo de documento:
Artigo
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