| Literature DB >> 9031001 |
M Yashiro1, H Nagoshi, Y Kasuga, H Isobe, S Kitajima, T Nakagawa, J Ohshima, K Ide, K Someya, N Saito.
Abstract
A 36-year-old woman who had had Graves' disease for 6 years was admitted with severe thrombocytopenia. Evans' syndrome was diagnosed. The patient's family history showed multiple cases of Graves' disease but no cases of Evans' syndrome. Both conditions in this patient improved with corticosteroid and thiamazole therapy. Several autoimmune antibodies were found, but a common autoimmune mechanism was not clearly shown. Although the combination of Graves' disease and Evans' syndrome had not occurred previously in her family, genetic factors may play an important role in the pathogenesis of both conditions.Entities:
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Year: 1996 PMID: 9031001 DOI: 10.2169/internalmedicine.35.987
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271