Exp Clin Endocrinol Diabetes 2005; 113(5): 302-307
DOI: 10.1055/s-2005-837551
Case Report

J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart · New York

Autoimmune Polyglandular Syndrome Associated with Idiopathic Giant Cell Myocarditis

C. Schumann1 , M. Faust1 , M. Gerharz2 , M. Ortmann2 , M. Schubert1 , W. Krone1
  • 1Department of Internal Medicine II, University of Cologne, Cologne, Germany
  • 2Institute of Pathology, University of Cologne, Cologne, Germany
Further Information

Publication History

Received: July 7, 2004 First decision: October 14, 2004

Accepted: March 15, 2005

Publication Date:
30 May 2005 (online)

Abstract

The autoimmune polyglandular syndrome (APS) is characterized by a variable coexistence of several autoimmune diseases, affecting predominantly endocrine glands. In general two types of APS are distinguished. Type 1 APS is an autosomal recessive disorder often leading to insufficiency of the adrenal cortex, the parathyroid glands, and/or the gonads. This type of APS often affects the skin in form of chronic mucocutaneous candidiasis and ectodermal dystrophies (vitiligo, alopecia, keratopathy, dystrophy of dental enamel and nails). The second form of APS is a polygenic disease which usually involves the adrenal gland, the thyroid and the pancreatic beta-cells. In rare cases APS type 2 is associated with myasthenia gravis, autoimmune thrombocytopenic purpura, Sjogren's syndrome or rheumatoid arthritis. Here we describe a case of APS with the unusual combination of type 1 diabetes, secondary adrenocortical insufficiency, growth hormone deficiency, and primary hypothyroidism associated with lethal idiopathic giant cell myocarditis. The combination of APS and idiopathic giant cell myocarditis which is a rare, frequently fatal autoimmune disorder of myocardium affecting most commonly young individuals has not been reported so far.

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