Cardiac myxoma

From WikiMD's Wellnesspedia

(Redirected from Atrial myxoma)

A myxoma is a rare benign tumor of the heart. Myxomas are the most common primary cardiac tumor in adults, and are most commonly found within the left atrium. Myxomas may also develop in the other heart chambers.[1] The tumor is derived from multipotent mesenchymal cells.[1]

Causes[edit | edit source]

Myxomas are the most common type of adult primary heart tumor.[1][2] Most myxomas arise sporadically (90%), and only about 10% are thought to arise due to inheritance.[3]

About 10% of myxomas are inherited, as in Carney syndrome. Such tumors are called familial myxomas. They tend to occur in more than one part of the heart at a time, and often cause symptoms at a younger age than other myxomas. Other abnormalities are observed in people with Carney syndrome include skin myxomas, pigmentation, endocrine hyperactivity, schwannomas and epithelioid blue nevi.[1] Myxomas are more common in women than men.[1][4]

Signs and symptoms[edit | edit source]

Symptoms may occur at any time, but most often they accompany a change of body position. Pedunculated myxomas can have a "wrecking ball effect", as they lead to stasis and may eventually embolize themselves. Symptoms may include:

The symptoms and signs of left atrial myxomas often mimic mitral stenosis. General symptoms may also be present, such as:

These general symptoms may also mimic those of infective endocarditis.

Complications[edit | edit source]

Diagnosis[edit | edit source]

A doctor will listen to the heart with stethoscope. A "tumor plop" (a sound related to movement of the tumor), abnormal heart sounds, or a murmur similar to the mid-diastolic rumble of mitral stenosis may be heard. These sounds may change when the patient changes position.

Right atrial myxomas rarely produce symptoms until they have grown to be at least 13 cm (about 5 inches) wide.

Tests may include:

Blood tests: A FBC may show anemia and increased WBCs (white blood cells). The erythrocyte sedimentation rate (ESR) is usually increased.

Treatment[edit | edit source]

The tumor must be surgically removed. Some patients will also need their mitral valve replaced. This can be done during the same surgery.

Myxomas may come back if surgery did not remove all of the tumor cells.

Prognosis[edit | edit source]

An embolized fragment of an atrial myxoma in the iliac bifurcation.

Although a myxoma is not malignant with risk of metastasis,[4] complications are common. Untreated, a myxoma can lead to an embolism (tumor cells breaking off and traveling with the bloodstream). Myxoma fragments can move to the brain, eye, or limbs.

If the tumor continues to enlarge inside the heart, it can block blood flow through the mitral valve and cause symptoms of mitral stenosis or mitral regurgitation. This may require emergency surgery to prevent sudden death.[7]

See also[edit | edit source]

References[edit | edit source]

  1. 1.0 1.1 1.2 1.3 1.4
  2. 4.0 4.1
  3. Eric J. Topol. The Topol Solution: Textbook of Cardiovascular Medicine, Third Edition with DVD, Plus Integrated Content Website, Volume 355. Lippincott Williams & Wilkins, Oct 19, 2006; page 223. ISBN 0781770122
  4. 6.0 6.1 "UOTW #31 - Ultrasound of the Week". Ultrasound of the Week. 30 December 2014. Retrieved 27 May 2017.
  5. "A Biatrial Myxoma with Triple Ripples".

External links[edit | edit source]

Classification
External resources

Wiki.png

Navigation: Wellness - Encyclopedia - Health topics - Disease Index‏‎ - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes

Search WikiMD


Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro) available.
Advertise on WikiMD

WikiMD is not a substitute for professional medical advice. See full disclaimer.

Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.


Contributors: Prab R. Tumpati, MD