| Literature DB >> 11795251 |
Helmut Laufs1, Peter Andrija Nigrovic, Lynda C Schneider, Hans Oettgen, Nido Pedro Del, Ivan P G Moskowitz, Elizabeth Blume, Antonio R Perez-Atayde.
Abstract
Giant cell myocarditis (GCM) is a rare and often fatal disease that infrequently affects children. Common variable immunodeficiency (CVID) describes a heterogeneous group of disorders characterized by hypogammaglobulinemia and poor specific antibody responses. To our knowledge, CVID and GCM have not been reported together in 1 patient. We describe a 12-year-old girl with CVID who developed acute severe GCM that necessitated cardiac transplantation. Histopathological and immunohistochemical studies of the endomyocardial biopsy specimen and the explanted heart revealed numerous histiocytes, eosinophils, T cells, and multinucleated giant cells. Both CVID and GCM are thought to involve dysregulation of T-cell function and have been associated with a similar spectrum of autoimmune conditions. The coincidence of CVID and GCM in a single patient may reflect a pathophysiologic connection.Entities:
Mesh:
Year: 2002 PMID: 11795251 DOI: 10.4065/77.1.92
Source DB: PubMed Journal: Mayo Clin Proc ISSN: 0025-6196 Impact factor: 7.616