A Case of Hemophagocytic Lymphohistiocytosis Accompanied by Acute Hepatitis A: Review of the Literature
Korean Journal of Hematology
; : 62-66, 2007.
Article
de Ko
| WPRIM
| ID: wpr-720135
Bibliothèque responsable:
WPRO
ABSTRACT
A previously healthy 26-year-old female was referred to our hospital because of fever and abnormalities of her blood biochemistry. Her laboratory results displayed leukopenia (1.79x103/microliter), thrombocytopenia (85x103/microliter), the serum aspartate aminotransferase and alanine aminotransferase levels were elevated to more than 2,000 IU/L, and the serum levels of lactate dehydrogenase and ferritin were markedly increased. Mild hepatosplenomegaly was reported on the abdomen-pelvis computed tomography. The bone marrow smears revealed proliferation of mature histiocytes that were ingesting platelets and erythrocytes, which is consistent with hemophagocytic lymphohistiocytosis. Although the other viral markers were all negative, the anti-hepatitis A IgM was positive and the anti-hepatitis A IgG was negative. Therefore, the patient was diagnosed as hepatitis A-associated hemophagocytic lymphohistiocytosis. Since a fulminant clinical course was suspected, 2 cycles of cyclosporine (3mg/kg iv from day 1 to day 5), dexamethasone (30mg iv qd from day1 to day 4) and immunoglobulin (500mg/kg iv day 1) therapy was started from the seventh day after onset and a favorable clinical outcome resulted.
Mots clés
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Aspartate aminotransferases
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Thrombopénie
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Biochimie
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Moelle osseuse
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Immunoglobuline G
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Immunoglobuline M
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Immunoglobulines
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Dexaméthasone
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Marqueurs biologiques
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Ciclosporine
Limites du sujet:
Adult
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Female
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Humans
langue:
Ko
Texte intégral:
Korean Journal of Hematology
Année:
2007
Type:
Article