Literature DB >> 10218385

A man with a mysterious hypogammaglobulinaemia and skin rash.

E E van Ginneken1, J W van der Meer, P M Netten.   

Abstract

We have observed a 26-year-old diabetic male who had been treated with carbamazepine because of seizures. After two months of treatment, he developed a severe illness with skin rash, fever, hepatomegaly and hypogammaglobulinaemia. Since hypogammaglobulinaemia is a rare side effect of carbamazepine treatment, a stop order was given for carbamazepine. The abnormalities (skin, fever, hypogammaglobulinaemia) remained until it appeared that the patient had secretly continued taking the drug. When drug administration was stopped the skin abnormalities improved and serum immunoglobulin levels became normal. The etiology of this transient carbamazepine-induced hypogammaglobulinaemia is unknown.

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Year:  1999        PMID: 10218385     DOI: 10.1016/s0300-2977(98)00140-5

Source DB:  PubMed          Journal:  Neth J Med        ISSN: 0300-2977            Impact factor:   1.422


  3 in total

1.  IgG2, IgG4 and IgA deficiency possibly associated with carbamazepine treatment.

Authors:  Zenichiro Kato; Mizuho Watanabe; Naomi Kondo
Journal:  Eur J Pediatr       Date:  2003-01-25       Impact factor: 3.183

2.  Antibody deficiency associated with carbamazepine.

Authors:  G Hayman; A Bansal
Journal:  BMJ       Date:  2002-11-23

3.  Oxcarbazepine-induced immunoglobulin deficiency.

Authors:  Adina Kay Knight; Charlotte Cunningham-Rundles
Journal:  Clin Diagn Lab Immunol       Date:  2005-04
  3 in total

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