| Literature DB >> 19901721 |
Shingo Konno1, Takamasa Ichijo, Mayumi Murata, Takahiro Toda, Hiroshi Nakazora, Nobuatsu Nomoto, Hideki Sugimoto, Hiroshi Nemoto, Teruyuki Kurihara, Nobuo Wakata, Toshiki Fujioka.
Abstract
We describe a rare case of autoimmune polyglandular syndrome type 2 initially presenting as Addison disease and autoimmune thyroid disease, with subsequent development of autoimmune hepatitis and myasthenia gravis (MG) crisis in a Japanese woman. MG improved with oral prednisolone followed by plasmapheresis for immunoadsorption; thymectomy was not performed. Conventional treatment for MG was effective and safe in this case, in which there was positivity for human leukocyte antigen A23, B52, B62, DR11, and DR15.Entities:
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Year: 2009 PMID: 19901721 DOI: 10.1097/NRL.0b013e3181945437
Source DB: PubMed Journal: Neurologist ISSN: 1074-7931 Impact factor: 1.398