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J Thorac Cardiovasc Surg 2007;133:1110-1111
© 2007 The American Association for Thoracic Surgery
Brief Communication |
a Department of Pediatric Oncology, Meram Medical School of Selcuk University, Konya, Turkey
b Department of Pediatrics, Meram Medical School of Selcuk University, Konya, Turkey
c Department of Thoracic Surgery, Meram Medical School of Selcuk University, Konya, Turkey.
Received for publication September 5, 2006; accepted for publication October 23, 2006. * Address for reprints: Olgun Kadir Aribas, MD, Selcuk Universitesi Meram Tip Fakultesi, Gogus Cerrahisi Anabilim Dali, 42080 Meram-Konya/Turkey. (Email: olgun@selcuk.edu.tr).
| The first 20% of the full text of this article appears below. |
Pulmonary sequestrations are rare congenital anomalies with an incidence of 0.15% to 1.7%, and they are divided into intralobar and extralobar pulmonary sequestrations (ELPS).1
A nonfunctioning pulmonary tissue characterizes them without normal connection to the tracheobronchial tree and supplying blood from 1 or more abnormal systemic arteries. Most ELPS are located between the lower lobe of the lung and the diaphragm; however, they may occur anywhere within the thorax and partially or completely within the diaphragm.1,2
In approximately 25% of patients with ELPS, different congenital lung abnormalities, such as hypoplasia, congenital cystic adenomatoid malformation, congenital lobar emphysema, or bronchogenic cyst, associated with ELPS are known.2
In this report, we present a child with an ELPS located in the upper posterior mediastinum associated with the azygos lobe.
Clinical Summary
A 5-year-old boy was referred to our hospital with a murmur in the mesocardiac area. His medical history was unremarkable. Physical examination results were normal except for a functional systolic murmur (1/°6). Blood biochemistry, complete blood count, and urinalysis results were normal. Chest radiography showed an
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