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


     


This Article
Right arrow Full Text (PDF)
Right arrow References
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):
Tommy L. Fudge
John L. Ochsner
Noel L. Mills
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 Fudge, T. L.
Right arrow Articles by Mills, N. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Fudge, T. L.
Right arrow Articles by Mills, N. L.

Ann Thorac Surg 1980;30:36-39
© 1980 The Society of Thoracic Surgeons


Articles

Clinical Spectrum of Pulmonary Hamartomas

Tommy L. Fudge, M.D., John L. Ochsner, M.D.*, Noel L. Mills, M.D.

From the Department of Surgery, Ochsner Medical Institutions, New Orleans, LA

* Address reprint requests to Dr. Ochsner, Ochsner Clinic, 1514 Jefferson Hwy, New Orleans, LA 70121

Pulmonary hamartomas are tumors that occur in the parenchyma or the bronchi. Though the lesions themselves are benign, they may be associated with malignant neoplasms or they may cause obstruction of the bronchi because of their location. Pulmonary hamartomas were resected in 29 patients at the Ochsner Medical Institutions during a 30-year period. Of these patients, 6 had symptoms related to concomitant malignancy and 3 had symptoms resulting from obstruction of the bronchi by the hamartoma.

Surgical treatment ranged from enucleation to pneumonectomy. One patient died in the hospital of extensive bronchogenic carcinoma. In 2 others, carcinoma of the lung developed within twelve months after resection of a hamartoma.

In this group of patients, 20% had concomitant or subsequent pulmonary lesions. Ten percent of the hamartomas were located in the bronchi, resulting in bronchial obstruction. A surgical approach is indicated for lesions that appear to be pulmonary hamartomas on roentgenograms.




This article has been cited by other articles:


Home page
J. Thorac. Cardiovasc. Surg.Home page
M. Ribet, S. Jaillard-Thery, and M. C. Nuttens
Pulmonary hamartoma and malignancy
J. Thorac. Cardiovasc. Surg., February 1, 1994; 107(2): 611 - 614.
[Abstract] [Full Text]


Home page
Ann. Thorac. Surg.Home page
B. A. Keagy, P. J. K. Starek, G. F. Murray, J. W. Battaglini, M. E. Lores, and B. R. Wilcox
Major Pulmonary Resection for Suspected but Unconfirmed Malignancy
Ann. Thorac. Surg., October 1, 1984; 38(4): 314 - 316.
[Abstract] [PDF]


Home page
Ann. Thorac. Surg.Home page
G. E. Hartman and S. J. Shochat
Primary Pulmonary Neoplasms of Childhood: A Review
Ann. Thorac. Surg., July 1, 1983; 36(1): 108 - 119.
[Abstract] [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 © 1980 by The Society of Thoracic Surgeons.