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Hemophagocytic Syndrome Associated with Kikuchi's Disease
Article in En | WPRIM | ID: wpr-23956
Responsible library: WPRO
ABSTRACT
A 13-yr-old female was admitted to our hospital with fever, seizure, and cervical lym-phadenopathy. Laboratory data showed pancytopenia, elevation of serum transaminase, lactate dehydrogenase, triglyceride, and ferritin levels. Lymph node biopsy revealed features of Kikuchi's disease and there were signs of histiocytosis and hemophagocytic phenomenon in bone marrow. She recovered after treatment with intravenous immunoglobulin and corticosteroids therapy. Hemophagocytic syndrome can be associated with Kikuchi's disease especially in childhood and seems to have a less aggressive clinical course and better prognosis.
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Full text: 1 Index: WPRIM Main subject: Pancytopenia / Prognosis / Triglycerides / Biopsy / Immunoglobulins / Bone Marrow Cells / Histiocytosis, Non-Langerhans-Cell / Adrenal Cortex Hormones / Histiocytic Necrotizing Lymphadenitis / Ferritins Type of study: Prognostic_studies Limits: Adolescent / Female / Humans Language: En Journal: Journal of Korean Medical Science Year: 2003 Type: Article
Full text: 1 Index: WPRIM Main subject: Pancytopenia / Prognosis / Triglycerides / Biopsy / Immunoglobulins / Bone Marrow Cells / Histiocytosis, Non-Langerhans-Cell / Adrenal Cortex Hormones / Histiocytic Necrotizing Lymphadenitis / Ferritins Type of study: Prognostic_studies Limits: Adolescent / Female / Humans Language: En Journal: Journal of Korean Medical Science Year: 2003 Type: Article