Asian Annals Click here to go to Medistim website
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
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):
Kadir Durgut
Ufuk Özergin
Right arrow Permission Requests
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Durgut, K.
Right arrow Articles by Özpinar, C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Durgut, K.
Right arrow Articles by Özpinar, C.
Related Collections
Right arrow Cardiac - other
Asian Cardiovasc Thorac Ann 2002;10:111-114
© 2002 Asia Publishing EXchange Pte Ltd


ORIGINAL CONTRIBUTIONS

Clinical Features and Surgical Treatment of Cardiac Myxoma: Report of 18 Cases

Kadir Durgut, MD, Niyazi Görmüs, MD, Mehmet Ozulku, MD, Ufuk Özergin, MD, Cevat Özpinar, MD

Department of Cardiovascular Surgery University of Selcuk School of Medicine Konya, Turkey
Kadir Durgut, MD Tel: 90 332 323 2600 Fax: 90 332 323 2643 email: kdurgut{at}selcuk.edu.tr Department of Cardiovascular Surgery, University of Selcuk School of Medicine, Akyokus, Meram, Konya 42080, Turkey.
Myxomas are the most common benign primary cardiac tumors. As many patients with cardiac myxoma suffer from cerebral or systemic embolism, which are serious complications, diagnosis of the tumor is vital. Between 1990 and 2000, 18 patients (6 males, 12 females), aged 24 to 73 years (mean, 55.3 years), were operated on for cardiac myxoma. The most common location of the myxoma was the left atrium (78%), and the transseptal surgical approach was preferred (78%) as it allows total resection of the left atrial myxoma along with its pedicle. Carney complex, a familial autosomal dominant form of atrial myxoma, was not found in any of the patients. There had been no operative or postoperative mortality and morbidity. The mean postoperative follow-up period was 5 years (mean, 1 to 10 years). No recurrence had been seen. We believe that the transseptal approach, in allowing total resection of the myxoma, prevents recurrence.







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 © 2002 by the Asia Publishing EXchange Ltd.