Case of the Month
Myasthenia gravis, castleman disease, pemphigus, and anti-phospholipid syndrome
Article first published online: 6 FEB 2013
DOI: 10.1002/mus.23657
Copyright © 2012 Wiley Periodicals, Inc., a Wiley company
Additional Information
How to Cite
Jakubíková, M., Piťha, J., Latta, J., Ehler, E. and Schutzner, J. (2013), Myasthenia gravis, castleman disease, pemphigus, and anti-phospholipid syndrome. Muscle Nerve, 47: 447–451. doi: 10.1002/mus.23657
Publication History
- Issue published online: 23 FEB 2013
- Article first published online: 6 FEB 2013
- Accepted manuscript online: 28 AUG 2012 03:27AM EST
- Manuscript Accepted: 24 AUG 2012
- Abstract
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Keywords:
- anti-phospholipid syndrome;
- Castleman disease;
- interleukin-6;
- myasthenia gravis;
- pemphigus vulgaris
Introduction: Myasthenia gravis is an autoimmune disease marked by neuromuscular transmission failure at the neuromuscular junction. Castleman disease is a rare lymphoproliferative disease characterized by non-cancerous angiofolicular hyperplasia of lymphatic tissue. Methods and results: We describe a young man with rapid, successive manifestations of myasthenia gravis, a solitary form of Castleman disease, pemphigus vulgaris, and anti-phospholipid syndrome, which resulted in 2 ischemic cerebrovascular events that caused a severe central neurological deficit. Discussion: We were unable to find a similar case in the literature, but we hypothesize that the temporal concidence of these clinical entities may be related to a common immunological pathway, such as B-cell activation. Therefore, we treated the patient with an immunosuppressant and anticoagulant treatment, as well as rituximab, a monoclonal antibody therapy against CD20+. Muscle Nerve 47:447-451, 2013

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