| Literature DB >> 12521216 |
Nozomu Kamei1, Kiminori Yamane, Yasuyo Yamashita, Shuhei Nakanishi, Hiroshi Watanabe, Rumi Fujikawa, Keiko Hiyama, Shinichi Ishioka, Ciro Mendoza, Nobuoki Kohno.
Abstract
Graves' disease (GD) has been reported to be frequently complicated with other autoimmune diseases. However, it is rarely complicated with scleroderma-polymyositis overlap syndrome. Recently, we encountered a 35-year-old woman who developed GD and immune thrombocytopenic purpura during follow-up observation of scleroderma-dermatomyositis overlap syndrome. Platelet counts recovered after high-dose gamma-globulin therapy and bolus methylprednisolone therapy. The present case is the first report of a combination of scleroderma, dermatomyositis, GD, and immune thrombocytopenic purpura. The patient was anti-Ku antibody-positive and had relatively low natural killer T cell counts, both of which might contribute to the complication of multiple autoimmune diseases.Entities:
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Year: 2002 PMID: 12521216 DOI: 10.2169/internalmedicine.41.1199
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271