ATS
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Personal Folders
Right arrow Download to citation manager
Right arrow Author home page(s):
David F Torchiana
Right arrow Permission Requests
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Dinh, M. H. T.
Right arrow Articles by Torchiana, D. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Dinh, M. H. T.
Right arrow Articles by Torchiana, D. F.

Ann Thorac Surg 2001;71:1673-1675
© 2001 The Society of Thoracic Surgeons


Case report

Left ventricular hamartoma associated with ventricular tachycardia

Minh H.T Dinh, BAa, Joseph M Galvin, MDb, Thomas H Aretz, MDc, David F Torchiana, MDa,*

a Division of Cardiac Surgery, Massachusetts General Hospital, Boston, Massachusetts, USA
b Division of Electrophysiology, Massachusetts General Hospital, Boston, Massachusetts, USA
c Department of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA

Accepted for publication July 10, 2000.

* Address reprint requests to Dr Torchiana, Department of Cardiac Surgery, Massachusetts General Hospital, 55 Fruit St, Boston, MA 02114 (Email: dtorchiana{at}partners.org).

Cardiac hamartomas are a rare type of benign tumor affecting the heart. We describe a 33-year-old patient who presented with a wide complex tachycardia. Diagnostic imaging revealed a mass in the patient’s left ventricular wall, near the apex of the heart. The mass was surgically resected and appeared benign. Its pathology was that of a hamartoma of mature cardiac myocytes. Postoperative electrophysiology evaluation showed no inducible focus and the patient remains alive and asymptomatic after 2 years of follow-up.




This article has been cited by other articles:


Home page
Veterinary PathologyHome page
H. M. Golbar, T. Izawa, M. Kuwamura, D. Fujita, K. Okamura, R. Yamazaki, Y. Tagami, H. Sasai, and J. Yamate
Cardiac Hamartoma in a Young Squirrel Monkey Who Died Suddenly
Veterinary Pathology, September 1, 2011; 48(5): 970 - 974.
[Abstract] [Full Text] [PDF]


Home page
Interact CardioVasc Thorac SurgHome page
A. Galeone, P. Validire, J.-B. Gayet, and F. Laborde
Hamartoma of mature cardiac myocytes of the pulmonary infundibulum
Interact CardioVasc Thorac Surg, December 1, 2009; 9(6): 1029 - 1031.
[Abstract] [Full Text] [PDF]


Home page
BMJ Case ReportsHome page
F. Zhang, N. Yin, B. Yin, S. Xu, and Y. Yang
Giant right atrial cystic hamartoma: a case report and literature review
BMJ Case Reports, June 1, 2009; 2009(jun01_2): bcr0220091587 - bcr0220091587.
[Abstract] [Full Text]


Home page
Eur Heart J Cardiovasc ImagingHome page
S. C. Menon, D. V. Miller, A. K. Cabalka, and D. J. Hagler
Hamartomas of mature cardiac myocytes
Eur Heart J Cardiovasc Imaging, November 1, 2008; 9(6): 835 - 839.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ANN THORAC SURG ASIAN CARDIOVASC THORAC ANN EUR J CARDIOTHORAC SURG
J THORAC CARDIOVASC SURG ICVTS ALL CTSNet JOURNALS
Copyright © 2001 by The Society of Thoracic Surgeons.