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J Thorac Cardiovasc Surg 2008;136:1080-1081
© 2008 The American Association for Thoracic Surgery
Brief Communication |
lu, MD*Department of Thoracic Surgery, Sureyyapasa Chest Disease and Thoracic Surgery Education and Research Hospital, Istanbul, Turkey
Received for publication October 18, 2007; accepted for publication November 29, 2007.
* Address for reprints: Semih Halezero
lu, MD, Sureyyapasa Chest Disease and Thoracic Surgery, Educational and Research Hospital, Maltepe 34758 Istanbul, Turkey. (Email: semihh{at}atlas.net.tr).
Although persistent left superior vena cava (PLSVC) is one of the most common congenital variations in the thoracic venous system, its resection for lung cancer has not been reported previously. We report partial resection of PLSVC together with a centrally located carcinoma in the left lung.
A 55-year-old man with a new onset of hemoptysis was admitted to the Sureyyapasa Chest Diseases and Thoracic Surgery Teaching and Research Hospital (Istanbul, Turkey). He had no history of previous disorders. Physical examination and routine laboratory tests showed normal results. A mass lesion in the left hilum was observed on chest x-ray. Fiberoptic bronchoscopy displayed an obstruction of the left upper lobe bronchus with a tumoral lesion. Pathology results of the biopsy showed squamous cell carcinoma. There was a 3-cm tumoral mass located in the left hilum of the lung adjacent to the pulmonary artery and vein on computed tomography (CT). A circular-shaped (10 mm in its biggest axes) paraaortic lesion seen on CT was evaluated as a benign lymph node (Figure 1 ).
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The postoperative period was uneventful. Definitive pathology revealed R0 resection with pathologic stage T4N0 resulting from both left atrium and vena cava invasion. Echocardiography was performed to investigate accompanying cardiac problems and revealed no abnormality. Venography was performed to demonstrate the postoperative grade of the PLSVC narrowing and the drainage pathway of the anomaly (Figure 2, B).
PLSVC is one of the most common congenital variations in the thoracic venous system with an incidence of 0.3% to 0.5% in the healthy population and 4.3% in those with congenital heart disease.1
During normal embryogenesis, failure of obliteration of the left cardinal vein results in PLSVC.2
In general, patients with PLSVC have a normal right superior vena cava (SVC) and no symptoms. However, Yamada and colleagues3
reported a patient with a left SVC but no right SVC. This condition usually requires no treatment and has no adverse effect on hemodynamic status when there is no associated cardiac abnormality. The importance of PLSVC is the greater prevalence of associated congenital cardiovascular defects and higher incidence of rhythm disorders. The most common associated lesion is an intra-atrial septal defect.4
For this reason, exclusion of concomitant heart disease is an important situation before undergoing a major operation.
The condition is usually diagnosed after the placement of a central venous catheter; catheter placement is generally difficult because advancement of the catheter is impeded, as occurred in our case. Manipulation of the venous lead through this unusual venous route may be associated with complications. Accurate diagnosis can be achieved by echocardiography in conjunction with Doppler or contrast ultrasonography with an appearance of a dilated, echo-free space posterior in the atrioventricular groove between the left atrium and the ventricle.4
In the present case, we misinterpreted PLSVC as a lymphadenopathy on horizontal CT slices in the preoperative period. Because of the rarity of the situation, a similar misdiagnosis was reported by Wong and Goldstraw.5
Resection of the right SVC for lung cancer in a setting of complete resection has been performed for years. This current case shows that partial resection of PLSVC in the case of its invasion by lung cancer is also possible.
References
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