Giant endobronchial hamartoma resected by fiberoptic bronchoscopy electrosurgical snaring

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Abstract

Less than 1% of lung neoplasms are represented by benign tumors. Among these, hamartomas are the most common with an incidence between 0.025% and 0.32%. In relation to the localization, hamartomas are divided into intraparenchymal and endobronchial. Clinical manifestation of an endobronchial hamartoma (EH) results from tracheobronchial obstruction or bleeding. Usually, EH localizes in large diameter bronchus. Endoscopic removal is usually recommended. Bronchotomy or parenchimal resection through thoracotomy should be reserved only for cases where the hamatoma cannot be approached through endoscopy, or when irreversible lung functional impairment occurred after prolonged airflow obstruction. Generally, when endoscopic approach is used, this is through rigid bronchoscopy, laser photocoagulation or mechanical resection. Here we present a giant EH occasionally diagnosed and treated by fiberoptic bronchoscopy electrosurgical snaring. © 2011 Mondello et al; licensee BioMed Central Ltd.

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Mondello, B., Lentini, S., Buda, C., Monaco, F., Familiari, D., Sibilio, M., … Barone, M. (2011). Giant endobronchial hamartoma resected by fiberoptic bronchoscopy electrosurgical snaring. Journal of Cardiothoracic Surgery, 6(1). https://doi.org/10.1186/1749-8090-6-97

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