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Case Report

Endobrnachial Hamartoma

The Ewha Medical Journal 1981;4(1):29-32. Published online: July 24, 2015

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.

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  • 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.

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