Surgical treatment of a giant cystic tumor of the atrioventricular nodal region.

Abstract:

:Cystic tumor of the atrioventricular nodal region is a rare cardiac primary tumor that can cause heart blockage and sudden death. Antemortem diagnosis and successful excision of the atrioventricular nodal region are extremely rare. A 41-year-old woman who presented with dyspnea and palpitations is reported. Electrocardiography revealed third-degree atrioventricular block. Echocardiography showed a right atrial cystic mass attached to the interatrial septum. The patient underwent surgical excision of the mass. Histopathological findings were of a cystic tumor of the atrioventricular nodal region. Placement of a permanent pacemaker was required for complete heart blockage. A two-year follow-up has revealed no sign of recurrence. This is the first case to be reported in China.

authors

Guo J,Zuo S,Lin C,Ji Y

doi

10.1510/icvts.2008.191866

subject

Has Abstract

pub_date

2009-05-01 00:00:00

pages

592-3

issue

5

eissn

1569-9293

issn

1569-9285

pii

icvts.2008.191866

journal_volume

8

pub_type

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