| Literature DB >> 16633932 |
Haruyo Iwadate1, Hiroko Kobayashi, Kiori Shio, Etsuko Noguchi, Kenya Watanabe, Tomomi Sasajima, Hideharu Sekine, Hiroshi Watanabe, Hiromasa Ohira, Katsutoshi Obara, Yukio Sato.
Abstract
We describe a 49-year-old woman who presented in 2002 with pure red cell aplasia (PRCA), systemic lupus erythematosus (SLE), and idiopathic portal hypertension (IPH) that developed following a thymectomy. She underwent a thymectomy at 40 years of age to treat myasthenia gravis. PRCA developed 3 years after the thymectomy and she was successfully treated with cyclosporin. Systemic lupus erythematosus and IPH were diagnosed 6 years later. We conclude that immunological dysfunction resulting from the thymectomy contributed significantly to the subsequent development of PRCA, SLE, and IPH in this patient. This is the first report to describe this extremely rare occurrence.Entities:
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Year: 2006 PMID: 16633932 DOI: 10.1007/s10165-006-0465-7
Source DB: PubMed Journal: Mod Rheumatol ISSN: 1439-7595 Impact factor: 3.023