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Two concomitant congenital lung malformations mimicking a paravertebral mass
Gokhan Haciibrahimoglu1, Umit Aydogmus2, Mehmet Ali Bedirhan2
1Thoracic Surgery Clinic, Medical Park Bahcelievler Hospital, Istanbul, Turkey ghaciibrahim@yahoo.com.
Asian Cardiovascular & Thoracic Annals
|July 11, 2014
Summary
A rare lung malformation, an extralobar pulmonary sequestration connected to a bronchogenic cyst, was found in a 47-year-old woman. Surgical resection successfully treated this unique asymptomatic condition.
Area of Science:
- Cardiothoracic Surgery
- Pulmonary Medicine
- Congenital Malformations
Background:
- Extralobar pulmonary sequestration (EPS) is a rare congenital lung malformation where lung tissue receives its blood supply from systemic arteries.
- Bronchogenic cysts are congenital lung malformations that arise from abnormal budding of the primitive foregut.
- The co-occurrence of EPS and bronchogenic cysts is exceptionally rare, posing diagnostic challenges.
Observation:
- A 47-year-old woman presented with an asymptomatic, unique malformation.
- The malformation involved an extralobar pulmonary sequestration communicating with a bronchogenic cyst.
- Preoperative imaging, including computed tomography and magnetic resonance imaging, failed to establish a definitive diagnosis.
Findings:
- The definitive diagnosis was made intraoperatively during a left thoracotomy.
- The surgical procedure involved the successful resection of both the sequestrated lobe and the communicating bronchogenic cyst.
- Histopathological examination confirmed the nature of the coexisting malformations.
Implications:
- This case highlights the diagnostic difficulties associated with rare combined pulmonary malformations.
- Early surgical intervention is crucial for managing symptomatic or incidentally discovered pulmonary sequestrations and bronchogenic cysts.
- Reporting such unique cases contributes to a better understanding of congenital lung anomalies and informs clinical management strategies.
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