Evans' Syndrome Associated with Graves' Disease

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 improv...

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Bibliographic Details
Published in:Internal Medicine Vol. 35; no. 12; pp. 987 - 990
Main Authors: YASHIRO, Miho, NAGOSHI, Haruhisa, KASUGA, Youko, ISOBE, Hozumi, KITAJIMA, Satoshi, NAKAGAWA, Teisuke, OHSHIMA, Jun, IDE, Kiyoshi, SOMEYA, Kazuhiko, SAITO, Nobuhiko
Format: Journal Article
Language:English
Published: Tokyo The Japanese Society of Internal Medicine 1996
Japanese Society of Internal Medicine
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Summary: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. (Internal Medicine 35: 987-990, 1996)
Bibliography:ObjectType-Case Study-3
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ISSN:0918-2918
1349-7235
DOI:10.2169/internalmedicine.35.987