(Circulation. 2002;105:1254.)
© 2002 American Heart Association, Inc.
Images in Cardiovascular Medicine |
From the Departments of Pathology (A.A., G.T.), Internal Medicine (A.R.), Pediatrics (G.S.M., O.M.), University of Padua Medical School, Padua, Italy.
Correspondence to Gaetano Thiene, MD, Cardiovascular Pathology Unit, Istituto di Anatomia Patologica, Via A. Gabelli, 61, 35100 Padova, Italy. E-mail cardpath@unipd.it
At 18 weeks of gestation, a 28-year-old woman with known connective tissue disease had a fetal echocardiogram that showed a complete atrioventricular block and endocardial fibroelastosis of the right ventricle with a focal hyperechogenic area at the crux cordis and mild pericardial effusion (Figure, a). At 22 weeks, the pregnancy was interrupted without complication, and the mother at present is well.
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Autopsy of the fetus showed no evidence of structural developmental cardiac defects (Figure,b). A lymphocytic myocarditis affecting mainly the atria and calcification of the sinoatrial and atrioventricular nodes were observed as the underlying histological abnormalities responsible for the congenital atrioventricular block (Figure, c through f). No infective agents could be detected by histochemical or immunohistochemical methods (Giemsa, Ziehl-Nielsen, Grocott, PAS, Gram, AntiToxo, anti-CMV).
In this report, we show that congenital complete heart block can be the consequence of fetal autoimmune lymphocytic myocarditis, which may, in
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