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Pulmonary arteriovenous fistula

Arteriovenous malformation - pulmonary

Pulmonary arteriovenous fistula is an abnormal connection between an artery and vein in the lungs. As a result, blood passes through the lungs without receiving enough oxygen.

Causes

Pulmonary arteriovenous fistulas are usually the result of abnormal development of the blood vessels of the lung. Most occur in people with Rendu-Osler-Weber disease (ROWD), now commonly called hereditary hemorrhagic telangiectasia (HHT). These people often have abnormal blood vessels in many other parts of the body.

Fistulas also can be a complication of liver disease or lung injury, although this is much less common.

Symptoms

Many people have no symptoms. When symptoms occur, they can include:

Exams and Tests

The health care provider will examine you. The exam may show:

  • Abnormal blood vessels (telangiectasias) on the skin or mucus membranes
  • Abnormal sound, called a murmur when a stethoscope is placed over the abnormal blood vessel
  • Low oxygen when measure with a pulse oximeter

 Tests that may be done include:

Treatment

A small number of people who have no symptoms may not need treatment. For most people with fistulas, the treatment of choice is to block the fistula during an arteriogram (embolization).

Some people may need surgery to remove the abnormal vessels and nearby lung tissue.

When arteriovenous fistulas are caused by liver disease, the treatment is a liver transplant.

Outlook (Prognosis)

The outlook for people with HHT is not as good as for those without HHT. For people without HHT, surgery to remove the abnormal vessels usually has a good outcome, and the condition is not likely to return.

Possible Complications

Complications may include:

  • Bleeding in the lung
  • Stroke due to blood clot that travels from the lungs to the arms, legs, or brain (paradoxical venous embolism)
  • Infection in the brain or heart valve, especially in patients with HHT

When to Contact a Medical Professional

Call your provider if you often have nosebleeds or difficulty breathing, especially if you also have a personal or family history of HHT.

For more information on testing, diagnostic, surgical and treatment services available at Huron Regional Medical Center, click here. The medical staff at HRMC includes full-time primary and specialty physicians to care for your whole family, as well as visiting specialists who see patients in HRMC'S Specialty Clinic, HRMC Physicians Clinic and other local clinics. Learn more by visiting our online Find-a-Doc directory.

Prevention

Because HHT is often genetic, prevention is not usually possible. Genetic counseling may help in some cases.

References

Shovlin CL, Jackson JE. Pulmonary vascular abnormalities. In: Broaddus VC, Mason RJ, Ernst JD, et al, eds. Murray and Nadel's Textbook of Respiratory Medicine. 6th ed. Philadelphia, PA: Elsevier Saunders; 2016:chap 61.

Stowell J, Gilman MD, Walker CM. Congenital thoracic malformations. In: Shepard JO, ed. Thoracic Imaging: The Requisites. 3rd ed. Philadelphia, PA: Elsevier; 2019:chap 8.

Webb GD, Smallhorn JF, Therrien J, Redington AN. Congenital heart disease in the adult and pediatric patient. In: Zipes DP, Libby P, Bonow RO, Mann DL, Tomaselli GF, Braunwald E, eds. Braunwald's Heart Disease: A Textbook of Cardiovascular Medicine. 11th ed. Philadelphia, PA: Elsevier; 2019:chap 75.


         

        Review Date: 7/20/2018

        Reviewed By: Allen J. Blaivas, DO, Division of Pulmonary, Critical Care, and Sleep Medicine, VA New Jersey Health Care System, Clinical Assistant Professor, Rutgers New Jersey Medical School, East Orange, NJ. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.

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