Superior vena cava obstruction

Last revised by Joshua Kogan on 28 May 2024

Superior vena cava obstruction (SVCO) can occur from extrinsic compression, intrinsic stenosis, or thrombosis of the superior vena cava. Malignancies are the main cause and are considered an oncologic emergency. Superior vena cava syndrome (SVCS) refers to the clinical syndrome with symptoms that results from this obstruction.

Clinical presentation depends on the speed, severity, and location of superior vena cava obstruction 5. Collateral drainage may develop with slow obstruction and patients may have no or only mild symptoms.

With acute superior vena cava obstruction, symptoms include facial and neck swelling, facial flushing, bilateral upper extremity swelling, neurological signs, dyspnea, headache, and cough.

The Pemberton maneuver 8 might be a useful physical examination tool. The maneuver is achieved by having the patient elevate both arms until they touch the sides of the face. A positive Pemberton sign is marked by the presence of facial congestion and cyanosis, as well as respiratory distress after approximately one minute.

In long-standing cases with 60% or more stenosis, collateral channels are formed to restore venous return. Various collaterals are formed depending on the site of the obstruction:

  • preazygos: in these conditions mainly the right superior intercostal veins serve as the collateral pathway to drain into the azygos vein

  • azygos: when the azygos vein is also obstructed the collateral circulation establishes between SVC and IVC via minor communicating channels i.e. internal mammary veins, superior and inferior epigastric veins to iliac veins, and finally into the IVC

  • post azygos: in this case, the blood from the SVC is distributed into the azygos and hemiazygos and then into the IVC tributaries i.e. ascending lumbar and lumbar veins

The most efficient collateral system is right superior intercostal and azygos circulation. For this reason, most of the patients with preazygos obstruction of superior vena cava remain asymptomatic for a long period of time.

See article: superior vena cava obstruction (grading).

Classically associated with a hot quadrate sign which is defined as increased CT/MRI enhancement or radiotracer accumulation isolated to the quadrate lobe of the liver. This is not to be confused with the hot caudate sign, which is classically associated with Budd-Chiari Syndrome.

Indirect signs on chest x-ray, such as superior mediastinal widening and right hilar prominence that may indicate the presence of mediastinal mass. Aortic nipple sign is also a feature.

Is the imaging modality of choice. Enhanced CT shows the location and severity of the superior vena cava obstruction, superimposed thrombosis, a mediastinal mass or lymphadenopathy, collateral vessels, and associated lung masses. A focal hepatic hot spot sign may be visible. There may also be pseudopathologic vertebral enhancement due to intraosseous collateral venous flow 9.

Treatment of superior vena cava syndrome will depend on the cause of the compression. Thrombolysis and anticoagulation may be indicated for thrombosis. In cases of compression, endovascular treatment with self-expandable bare stents is an effective superior vena cava syndrome therapy 6. With carcinoma or infection, specific drugs or radiation may be used 7.

Acute superior vena cava obstruction may lead to:

  • cerebral edema

  • laryngeal edema

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