Case Report

Endobrnachial Hamartoma

Yorng Man Choi
Author Information & Copyright
Department of General Surgery, College of Medicine, Ewha Womans University, Korea.
Corresponding author: Yorng Man Choi. Department of General Surgery, College of Medicine, Ewha Womans University, Korea.

Copyright ⓒ 1981. Ewha Womans University School of Medicine. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Published Online: Jul 24, 2015

Abstract

Pulmonary chondromatous hamartoma is a very rare disease in pulmonary tumors but it's character is benign nature. It is often incidental, asymptomatic finding on routine chest roentgenogram. They are reported to account for 8 percent of all coin lesions. In 1904, Albrecht first used the term "Hamartoma" to refer to a cogenital abnormal mixing of the normal components of an organs other than the lung. The author experienced one case of endobronchial hamartoma. The patient, 41-year-old-female was admitted to our hospital due to chest tightness and general weakness. Chest roentgenogram reveals that walnut-size radio-opaque density is seen in right upper lung field with demarcated margin. Right pneumonectomy is performed and the answer of pathology is benignendotrachial hamartoma. The post-operative course is unevenful and she was discharged in good condition.



PDF Download
PubReader
Export Citation

Metrics

View
486
Download
150
Crossref
0
Endobrnachial Hamartoma

QR Code of this Article: