Abstract
We describe the case of a pediatric patient on azathioprine therapy with previously undiagnosed homozygote thiopurine S-methyltransferase (TPMT) deficiency, resulting in myelotoxic thiopurine metabolite levels. The patient was successfully treated with a very low azathioprine dose of 50 mg once a week (4% of standard dose), guided by frequent thiopurine metabolite measurement and a close clinical surveillance. We demonstrate that azathioprine therapy still might be an effective and safe therapeutic option in pediatric thiopurine S-methyltransferase-deficient IBD patients.
MeSH terms
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Adolescent
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Azathioprine / administration & dosage
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Azathioprine / adverse effects
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Azathioprine / therapeutic use*
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Dose-Response Relationship, Drug
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Drug Hypersensitivity / complications*
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Drug Hypersensitivity / diagnosis
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Drug Monitoring / methods
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Humans
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Immunosuppressive Agents / administration & dosage
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Immunosuppressive Agents / adverse effects
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Immunosuppressive Agents / therapeutic use*
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Inflammatory Bowel Diseases / drug therapy*
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Male
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Purine-Pyrimidine Metabolism, Inborn Errors / complications*
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Purine-Pyrimidine Metabolism, Inborn Errors / diagnosis
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Treatment Outcome
Substances
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Immunosuppressive Agents
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Azathioprine
Supplementary concepts
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Thiopurine S methyltranferase deficiency