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AJR 2001; 176:211-213
© American Roentgen Ray Society


Case Report

Systemic-to-Pulmonary Venous Shunt in Superior Vena Cava Obstruction Revealed on Dynamic Helical CT

David Grayet1, Benoit Ghaye, David Szapiro and Robert F. Dondelinger

1 All authors: Department of Medical Imaging, University Hospital Sart Tilman B35, B-4000 Liege 1, Belgium.

Received January 27, 2000; accepted after revision June 2, 2000.

 
Address correspondence to R. F. Dondelinger.


Introduction
Top
Introduction
Case Report
Discussion
References
 
Obstruction of the superior vena cava is frequently associated with the formation of collateral veins involving mainly the azygos-hemiazygos system, the paravertebral venous network, and the internal and lateral thoracic veins. Systemic-to-pulmonary venous shunts may also occur in rare cases [1]. These shunts consist of mediastinal connections between the innominate veins and the superior pulmonary veins, through bronchial venous plexuses developed around the airways, hilar vessels, and pleura. We report two patients in whom these shunts were shown on angiodynamic helical CT and three-dimensional reformatting.


Case Report
Top
Introduction
Case Report
Discussion
References
 
A 58-year-old man was admitted to the hospital for progressive hoarseness, dysphonia, and cough. The patient also complained of headache and dizziness. His medical history included myocardial infarction treated by aortocoronary bypass. Physical examination showed right lateral swelling of the neck and right vocal cord palsy. Chest radiographic findings revealed a right-sided hilar mass, widening of the right tracheal stripe, and tracheal displacement. The carcinoembryonic antigen level was 14.7 ng/mL (normal level, <5 ng/mL), and the neuron-specific enolase level was 15.8 ng/mL (normal level, <12.5 ng/mL). Bronchoscopy showed moderate extrinsic compression of the tracheal lumen and infiltration of the distal trachea and right mainstem bronchial wall. Transbronchial biopsy confirmed small cell lung cancer.

Thoracic staging was performed using helical CT (PQ 5000; Picker International, Cleveland, OH). Two consecutive acquisitions were obtained after the IV injection of 120 mL of ioversol ([300 mg I/mL] Optiray; Guerbet, Aulnay-sous-Bois, France) through a right upper arm vein with a power injector at a rate of 2 mL/sec. The patient was placed supine with the arms elevated to minimize artifacts. The first helical scan, obtained 20 sec after the start of injection, included the area from the right inferior pulmonary vein to the cervicothoracic junction. The scanning protocol was as follows: 5-mm slice thickness, 3-mm increment, and a pitch of 1.5. The next helical scan covered the lung bases using a slice thickness of 10 mm, an increment of 8 mm, and a pitch of 1.5. Sequential high-resolution CT was performed, covering the entire lung at 10-mm intervals. Helical CT data were transferred to a work-station (Voxel Q; Picker International). Maximum-intensity-projection and volume-rendering reconstructions were obtained in various projections.

CT showed a tight stenosis of the superior vena cava and an occlusion of both innominate veins at the confluence caused by a bulky 6.5 x 4 x 9.5 cm mass extending from the right pulmonary hilum to the right lateral aspect of the trachea. The left superior pulmonary vein and the left heart were intensely opacified before opacification of the right heart and the pulmonary artery (Fig. 1A,1B,1C). This right-to-left shunt was related to early filling of mediastinal venous collaterals connecting the left innominate vein and the left superior pulmonary vein. Other collateral venous pathways, such as the azygos and hemiazygos veins, the right internal thoracic vein, and the vertebral venous plexus, were also seen. Despite systemic chemotherapy with cisplatin (Platinol; Bristol-Myers Squibb, Brussels, Belgium) and etoposide (Vepesid; Bristol-Myers Squibb), the superior vena cava syndrome worsened, and the patient was treated with corticosteroids and adjuvant radiotherapy.



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Fig. 1A. 58-year-old man with systemic-to-pulmonary venous shunt. Helical CT scan shows tight stenosis of superior vena cava (curved arrow) and obstruction of distal part of left innominate vein (open arrow) caused by tumor encasement (T). Mediastinal venous network is densely opacified (small white arrows). Note opacification of azygos vein (thick white arrow), accessory hemiazygos vein (arrowhead), and perivertebral plexus.

 


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Fig. 1B. 58-year-old man with systemic-to-pulmonary venous shunt. Helical CT scan 3 cm caudal to A shows early enhancement of aorta (236 H) after IV contrast injection (pulmonary artery, 180 H). Note opacification of right internal thoracic vein (thick arrow), opacified dilated bronchial veins (arrowheads), and mediastinal venous network (small arrows).

 


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Fig. 1C. 58-year-old man with systemic-to-pulmonary venous shunt. Helical CT scan 2 cm caudal to B shows left superior pulmonary vein (asterisk), dilated bronchial veins (arrowheads) and mediastinal venous network (small arrows) with higher attenuation (500 and 1250 H, respectively) than superior vena cava, pulmonary artery, and right superior pulmonary vein (180 H) (thick arrow).

 

CT performed after treatment showed reduction in the size of the mass to a diameter of 1 cm. Right and left innominate veins were patent. Venous collaterals were no longer observed, and sequential opacification of cardiac chambers was unremarkable.


Discussion
Top
Introduction
Case Report
Discussion
References
 
Systemic-to-pulmonary venous shunt is a condition that is reported in the literature only in isolated case reports [1]. These right-to-left shunts are typically associated with superior vena cava obstruction, usually caused by malignant tumor and rarely caused by benign conditions. Classically, in cases of superior vena cava obstruction, blood drains into the azygos-hemiazygos system, the lateral and internal thoracic veins, and the paravertebral network [2]. Unusual connections may be established between a systemic vein and a pulmonary vein that result in a right-to-left shunt. These shunts can be formed by different mechanisms: anatomic, congenital, or acquired.

In the anatomic type, bronchial veins and pulmonary veins are interconnected through already existing bronchial venous plexuses. These plexuses are located in the bronchial wall and the peribronchovascular connective tissue, acting as vasa vasorum. As a result, bronchial veins predominantly drain into the right atrium through the pleurohilar bronchial veins, and approximately one third of their flow is into the left atrium through the pulmonary veins [3,4,5]. In normal conditions, the pleurohilar bronchial veins communicate with the azygos and hemiazygos veins. Valves are usually located at the junction of pleurohilar bronchial veins with azygos and hemiazygos veins, preventing backflow into the pleurohilar bronchial veins. If pressure rises (as occurs in cases of superior vena cava obstruction), the valves may become incompetent, resulting in a right-to-left shunt by reversed flow. The right-to-left shunt is most likely of the anatomic type.

In the congenital type of shunt, three shunting pathways are distinguished: an aberrant pulmonary venous return with reversed flow, a levoatriocardinal embryologic remnant (connecting the posterior cardinal system with pulmonary veins) [6, 7], and a persistent left superior vena cava (occasionally seen as a thin channel draining into the right atrium or, rarely, into the left superior pulmonary vein or left atrium). The acquired shunt is basically of inflammatory origin and results in newly formed vessels bridging the subpleural pulmonary veins and the intercostal veins through pleural adhesions [1].

In our first patient, imaging revealed the shunt's location in a normal pleuropulmonary area, thus excluding the possibility of an acquired shunt. Furthermore, no unique shunting vein was shown on CT, but rather several dilated pleurohilar bronchial veins draining into the left pulmonary vein, thus excluding a congenital shunt.

The second patient was a 70-year-old woman who was admitted for cervical and periscapular edema extending to both arms. Her medical history included a right-sided mastectomy and axillary lymphadenectomy for infiltrative ductal epidermoid carcinoma, followed by radiotherapy and chemotherapy. Angiodynamic helical CT showed stenosis of the superior vena cava and occlusion of the azygos vein caused by mediastinal adenopathy. The lateral and internal thoracic, azygos, and perivertebral veins were visualized, as was early opacification of the right superior pulmonary vein preceding opacification of the pulmonary arteries (Fig. 2). The shunt was located in the right upper lobe and no unique shunting vein was seen, thereby excluding a congenital shunt. The pleurohilar bronchial veins drained into the right superior pulmonary vein.



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Fig. 2. 70-year-old woman with systemic-to-pulmonary venous shunt. Helical CT scan shows earlier enhancement of right branches of superior pulmonary vein (thick arrows), dilated bronchial veins (arrowheads), and mediastinal venous network (small arrow) than of aorta, left pulmonary vein (asterisk), and pulmonary artery. Aorta (192 H) shows higher attenuation than pulmonary artery (148 H), indicating presence of right-to-left shunt.

 

Reported methods for depicting a right-to-left shunt include radionuclide studies using 99mTc-aggregated albumin [8] and phlebography [9]. Conventional [1] and helical [10] CT are also reported to be occasionally diagnostic.

In our patients, angiodynamic helical CT showed the right-to-left shunts and their locations, giving information superior to that of other imaging techniques. Angiodynamic helical CT revealed early contrast enhancement of the left heart or pulmonary veins before pulmonary arteries and showed the filling of pleurohilar bronchial veins.


References
Top
Introduction
Case Report
Discussion
References
 

  1. Stockberger SM, West KW, Cohen MD. Right-to-left shunt from systemic venous to pulmonary venous system developing after SVC obstruction. J Comput Assist Tomogr 1995;19:312 -315[Medline]
  2. Mendelson DS, Berson BD, Janus CL, Gendal ES, Krellenstein DJ. Computed tomography of mediastinal collaterals in SVC syndrome. J Comput Assist Tomogr 1988;12:881 -884[Medline]
  3. Liebow AA. The bronchopulmonary venous collateral circulation with special reference to emphysema. Am J Pathol 1953;29:251 -289
  4. Murata K, Itoh H, Todo G, et al. Bronchial venous plexus and its communication with pulmonary circulation. Invest Radiol 1986;21:24 -30[Medline]
  5. Ohmichi M, Tagaki S, Nomura N, Tsunematsu K, Suzuki A. Endobronchial changes in chronic pulmonary venous hypertension. Chest 1984;6:1127 -1132
  6. Blieden LC, Schneeweiss A, Deutsch V, Neufeld HN. Anomalous venous connection from the left atrium to the cardinal venous system: "levoatriocardinal vein." AJR 1977;129:937 -938[Medline]
  7. Bernstein HS, Moore P, Stanger P, Silverman NH. The levoatriocardinal vein: morphology and echocardiographic identification of the pulmonary-systemic connection. Am J Cardiol 1995;26:995 -1001
  8. Hutchins WW, Kirchner PT, MacMahon H. Perfusion lung scan in superior vena cava obstruction: demonstration of venous collaterals and systemic-pulmonary venous shunt. AJR 1982;138:754 -756[Free Full Text]
  9. Wilson ES. Systemic to pulmonary venous communication in the superior vena caval syndrome. AJR 1976;127:24 -249
  10. Schepers-Bok R, Mallens WMC. Obstruction of the vena cava due to aortic dissection: CT findings of collateral flow via the bronchial veins. Eur Radiol 1996;6:753 -755[Medline]

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