Circulation, Vol 56, 667-678, Copyright © 1977 by American Heart Association
TN James and I Galakhov
Benign congenital polycystic tumors of the atrioventricular (A-V) node are
an unusual but not very rare cause of heart block. Two such cases are
presented and discussed in conjunction with the reported experience of
other. The tumor is always within and only very near the A-V node, seldom
involves more than the proximal end of the His bundle, and has not been
reported to occur in the sinus node. Although sudden death has been
reported in conjunction with these tumors, a surprising number of other
patients have lived to old age and died of causes unrelated to the A-V
nodal tumor. As a corollary it is important to consider a diagnosis of A-V
nodal tumor in any patient of any age who presents with otherwise
unexplained heart block or syncope. From accumulated experience it appears
that such patients do not tolerate electronic pacing safely and some
possible explanations for this are discussed. Escape rhythm in all reported
cases has been characterized by QRS complexes which are narrow and a
ventricular rate which is from half to two-thirds of the sinus rate.
Reasons why an A-V junctional rhythm which is 66% of sinus rate may be
especially stable are discussed.
ARTICLES
De subitaneis mortibus. XXVI. Fatal electrical instabiltiy of the heart associated with benign congenital polycystic tumor of the atrioventricular node
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