Treatment of Methimazole-lnduced Severe Aplastic Anemia with Recombinant Human Granulocyte-Monocyte Colony-Stimulating Factor and Glucocorticosteroids
Author(s) -
Xavier LópezKarpovitch,
Alfredo UlloaAguirre,
Carlos von Eiff,
Rafael Hurtado-Monroy,
Alfonso J. Alanis
Publication year - 1992
Publication title -
acta haematologica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.574
H-Index - 56
eISSN - 1421-9662
pISSN - 0001-5792
DOI - 10.1159/000204742
Subject(s) - aplastic anemia , medicine , granulocyte , granulocyte colony stimulating factor , monocyte , recombinant dna , immunology , platelet , anemia , granulocyte macrophage colony stimulating factor , methimazole , in vivo , pharmacology , chemotherapy , cytokine , bone marrow , biology , biochemistry , thyroid , gene , microbiology and biotechnology
The in vivo response to recombinant human granulocyte-monocyte colony-stimulating factor (rHu GM-CSF) in facilitating the reconstitution of granulomonopoiesis was evaluated in a patient with Graves' disease who developed severe aplastic anemia during methimazole therapy. After 10 days of treatment with rHu GM-CSF, the neutrophil and monocyte counts rose to 1.65 x 10(9)/l and 0.41 x 10(9)/l, respectively. However, the patient was still dependent on erythrocyte and platelet transfusions. Two days after rHu GM-CSF withdrawal, the neutrophil count dropped off to 0.41 x 10(9)/l.rHu GM-CSF was reinitiated for 2 days along with glucocorticosteroids. With this combined therapeutic approach, the neutrophil count returned to normal and remained stable, and both Hb and platelet values began to improve. It is concluded that the combination of rHu GM-CSF and glucocorticosteroids can be used as a therapeutic option that may lead to beneficial results in drug-induced aplastic anemia.
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