Arteriovenous malformation

Arteriovenous malformation
Classification and external resources
Micrograph of an arteriovenous malformation in the brain. HPS stain.
ICD-10	Q27.3, Q28.0, Q28.2
ICD-9	747.6, 747.81
DiseasesDB	15235
MedlinePlus	000779
eMedicine	topic list
MeSH	D001165

Arteriovenous malformation or AVM is an abnormal connection between veins and arteries, usually congenital. This pathology is widely known because of its occurrence in the central nervous system, but can appear in any location. An arteriovenous malformation is a vascular anomaly. It is a RASopathy.

The genetic transmission patterns of AVM, if any, are unknown. AVM is not generally thought to be an inherited disorder, unless in the context of a specific hereditary syndrome.

Contents 1 History 2 Definition 3 Signs and symptoms 4 Genetics 5 Pathophysiology 6 Diagnosis 7 Treatment 8 Epidemiology 9 Society and culture 10 Research directions 11 See also 12 References 13 External links

History

Emmanuel, Luschka, and Virchow first described arteriovenous malformations in the mid 1800s. Olivecrona performed the first surgical excision of an intracranial AVM in 1932.

Definition

AVMs are lesions of the vasculature that develop such that blood flows directly from the arterial system to the venous system without passing through a capillary system.

Signs and symptoms

Symptoms of AVM vary according to the location of the malformation. Roughly 88%^[1] of people affected with AVM are asymptomatic; often the malformation is discovered as part of an autopsy or during treatment of an unrelated disorder (called in medicine "an incidental finding"); in rare cases its expansion or a micro-bleed from an AVM in the brain can cause epilepsy, deficit or pain.

The most general symptoms of a cerebral AVM include headache and epilepsy, with more specific symptoms occurring that normally depend on the location of the malformation and the individual. Such possible symptoms include:^[2]

• Difficulties with movement or coordination, including muscle weakness and even paralysis;
• vertigo (dizziness);
• Difficulties of speech (dysarthria) and communication, such as aphasia;
• Difficulties with everyday activities, such as apraxia;
• Abnormal sensations (numbness, tingling, or spontaneous pain);
• Memory and thought-related problems, such as confusion, dementia or hallucinations.

Cerebral AVMs may present in a number of ways

• Hemorrhage (45% of cases)
  • Acute onset of severe headache. May be described as the worst headache of the patient's life. Depending on the location of hemorrhage, may be associated with new fixed neurologic deficit. In unruptured brain AVMs, the risk of spontaneous hemorrhage may be as low as 1% per year. After a first rupture, the annual bleeding risk may increase to more than 5%.^[3]

• Seizure (46%)

• Headache (34%)

• Progressive neurologic deficit (21%)
  • May be caused by mass effect or venous dilatations. Presence and nature of deficit depend on location of lesion and the draining veins.^[4]

• Pediatric patients
  • Heart failure
  • Macrocephaly
  • Prominent scalp veins

Genetics

Pathophysiology

Arteriovenous malformations, also known as AVMs, are deficiencies of the cardiovascular system. In a normal functioning human body, arteries carry oxygen-rich blood away from the heart to the rest of the body, and veins return oxygen-depleted blood to the lungs and heart. An AVM interferes with this cyclical process. Instead of the gradual transition through the capillaries from arteries to veins that is typical of normal functioning vasculature, AVMs cause direct associations of the arteries and veins. AVMs can cause intense pain and lead to serious medical problems. Although AVMs are often associated with the brain and spinal cord, they can develop in any part of the body.

Arteries and veins are part of the human cardiovascular system. Normally, the arteries in the vascular system carry oxygen-rich blood, except in the case of the pulmonary artery. Structurally, arteries divide and sub-divide repeatedly, eventually forming a sponge-like capillary bed. Blood moves through the capillaries, giving up oxygen and taking up waste products, including CO₂, from the surrounding cells. Capillaries in turn successively join together to form veins that carry blood away. The heart acts to pump blood through arteries and uptake the venous blood.

An AVM lacks the dampening effect of capillaries on the blood flow; it also causes the surrounding area to be deprived of the functions of the capillaries — removal of CO₂ and delivery of nutrients to the cells. The resulting tangle of blood vessels, often called a nidus (Latin for "nest") has no capillaries and abnormally direct connections between high-pressure arteries and low-pressure veins. It can be extremely fragile and prone to bleeding. The resultant sign, audible via stethoscope, is a rhythmic, whooshing sound caused by excessively rapid blood flow through the arteries and veins. It has been given the term "bruit", French for noise. On some occasions a patient with a brain AVM may become aware of the noise, which can compromise hearing and interfere with sleep in addition to causing psychological distress.

Diagnosis

AVMs can occur in various parts of the body:

• brain, causing a cerebral arteriovenous malformation
• spleen^[5]
• lung^[6]
• kidney^[7]
• spinal cord^[8]
• liver^[9]
• intercostal space^[10]
• iris^[11]
• spermatic cord^[12]

AVMs may occur in isolation or as a part of another disease (for example, Von Hippel-Lindau disease or hereditary hemorrhagic telangiectasia).

AVMs have been shown to be associated with Aortic Stenosis.^[13]

Bleeding from an AVM can be relatively mild or devastating. It can cause severe and less often fatal strokes. If a cerebral AVM is detected before a stroke occurs, usually the arteries feeding blood into the nidus can be closed off to avert the danger. However, interventional therapy may also be relatively risky

Treatment

Treatment for brain AVMs can be symptomatic, and patients should be followed by a neurologist for any seizures, headaches or focal deficits. AVM-specific treatment may also involve endovascular embolization, neurosurgery or radiation therapy.^[2] Embolization, that is, cutting off the blood supply to the AVM with coils or particles or glue introduced by a radiographically guided catheter, can be used in addition to either, but is rarely successful in isolation except for in smaller AVMs. The neurological risk of any such intervention is roughly 10%. For unruptured brain AVMs, the benefit for endovascular, neurosurgical or radiation therapy is as yet unknown. Therefore, the best way to follow an unruptured brain AVM is to join the NIH/NINDS funded international study designed for patients with an unruptured brain AVM.^[14]

Epidemiology

The estimated detection rate of AVM in the US general population is 1.4/100,000 per year.^[15] This is approximately one fifth to one seventh the incidence of intracranial aneurysms. An estimated 300,000 Americans have AVMs, of whom 12% (approximately 36,000) will exhibit symptoms of greatly varying severity.^[2]

Society and culture

• On December 13, 2006, Senator Tim Johnson was diagnosed with AVM and treated at George Washington University Hospital.^[16]

• On August 3, 2011, Mike Patterson of the Philadelphia Eagles collapsed on the field and suffered a seizure during a practice. After he collapsed, Patterson was rushed to the hospital where he quickly texted Eagles employees and teammates that he was fine. He was described as alert and stable in the hospital, where he stayed overnight. Patterson was diagnosed with AVM on August 4.^[17]

• Six Feet Under, an American television series that ran on HBO from 2001–2005, featured a protaganist, Nate Fisher, that suffered from AVM, a recurring feature in the storyline of this character.

• On August 1, 2007, NIH/NINDS decides to launch the first international study evaluating the best treatment strategy for patients with unruptured brain AVMs: ARUBA — A Randomizd trial of Unruptured Brain AVMs.^[18]

• Actor Ricardo Montalbán was born with spinal AVM.^[19] During the filming of the 1951 film, Across the Wide Missouri, Montalbán was thrown from his horse, knocked unconscious, and trampled by another horse which aggrevated his AVM and resulted in a painful back injury that never healed. The pain increased as he aged, and in 1993, Montalbán underwent 9½ hours of spinal surgery which left him paralysed below the waist and using a wheelchair.^[20][21]

Research directions

Despite many years of research, the central question of whether to treat AVMs has not been answered. All treatments, whether involving surgery, radiation, or drugs, have risks and side-effects. Therefore it might be better in some cases to avoid treatment altogether and simply accept a small risk of coming to harm from the AVM itself. This question is currently being addressed in clinical trials.^[22] Interested patients are welcome to contact participating centers worldwide.

See also

• Foix-Alajouanine syndrome

References

External links

• AVM Support Groups from the DMOZ Open Directory.
• University of California San Francisco AVM research.
• http://www.arubastudy.org
• http://www.cervco.fr

Congenital vascular defects / Vascular malformation (Q25–Q28, 747) Great arteries/ other arteries Aorta Patent ductus arteriosus · Coarctation of the aorta · Interrupted aortic arch · Overriding aorta · Aneurysm of sinus of Valsalva · Vascular ring Pulmonary artery Pulmonary atresia · Stenosis of pulmonary artery Subclavian artery Aberrant subclavian artery Umbilical artery Single umbilical artery Great veins Superior/inferior vena cava Congenital stenosis of vena cava · Persistent left superior vena cava Pulmonary vein Anomalous pulmonary venous connection (Total, Partial) · Scimitar syndrome Arteriovenous malformation Cerebral arteriovenous malformation M: VAS anat(a:h/u/t/a/l,v:h/u/t/a/l)/phys/devp/cell/prot noco/syva/cong/lyvd/tumr, sysi/epon, injr proc, drug(C2s+n/3/4/5/7/8/9)