Abstract
In the past decade, understanding of the natural history and effect of immunosuppression and transplantation on idiopathic giant cell myocarditis (IGCM) has advanced significantly. IGCM was first described by Sergius Saltikow in a 37 year old man who died suddenly.1 Subsequently dozens of case reports and a few small series documented that IGCM is usually a fatal disorder that generally affects young, otherwise healthy individuals, although, a minority of cases occur in association with autoimmune disorders or thymoma.
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Cooper, L.T. (2003). Recent Advances in Giant Cell Myocarditis. In: Matsumori, A. (eds) Cardiomyopathies and Heart Failure. Developments in Cardiovascular Medicine, vol 248. Springer, Boston, MA. https://doi.org/10.1007/978-1-4419-9264-2_29
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DOI: https://doi.org/10.1007/978-1-4419-9264-2_29
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