Fibromuscular dysplasia
Updates to Article Attributes
Fibromuscular dysplasia (FMD) is a heterogeneous group of vascular lesions characterised by an idiopathic, non-inflammatory, and non-atherosclerotic angiopathy of small and medium-sized arteries.
Epidemiology
The prevalence is unknown 7. It is most common in young women with a female to male ratio of 3:1, and is typically diagnosed between the ages of 30 and 50 4.
Clinical presentation
Fibromuscular dysplasia is frequently asymptomatic. Symptomatic patients commonly present with:
- hypertension, or less commonly renal impairment, due to renal artery stenosis
- CNS symptoms (e.g. headache, neck pain, pulsatile tinnitus, Horner syndrome) from transient ischaemic attack, stroke, dissection, due to carotid and vertebral artery involvement 11
- angina, myocardial infarction or sudden cardiac death due to coronary artery involvement 10
- symptoms of mesenteric ischaemia (mesenteric infarction is rare due to the formation of collateral supply) 11
Pathology
The exact cause is not well known. The underlying pathology is a fibrous or fibromuscular thickening of the arterial wall. Any layer of the vessel wall may be affected: intima, media or adventitia. There is an absence of inflammatory cells 1-4,7.
Location
Fibromuscular dysplasia may affect any medium-sized artery in the body and is commonly multifocal and bilateral (up to 60% when involving the renal arteries). Fibromuscular dysplasia usually involves the mid-segment of vessels and spares origins. Some sites are more frequently involved 9:
- renal arteries (most common): estimated between ~5% (range 4-6%) in the renal arteries 7
-
cervicoencephalic arteries (next most common): estimated prevalence ~1.5% (range 0.3-3%) 7
- extracranial internal carotid arteries
- vertebral arteries
- iliac arteries
- coeliac trunk and mesenteric arteries
- subclavian and axillary arteries
- coronary arteries17
Classification
Fibromuscular dysplasia is classified into five categories according to the vessel wall layer affected:
- intima: 5%
- intimal fibroplasia (see carotid intimal fibromuscular dysplasia)
- media: 90-95%
- medial dysplasia (70%, commonest type)
- perimedial (subadventitial) fibroplasia (15-20%)
- medial hyperplasia (8-10%)
- adventitia: rare
- adventitial fibroplasia (1%) 8
The outcome is arterial stenoses. Fibromuscular dysplasia most commonly causes small stenoses along a vessel with intervening areas of dilatation (small aneurysms), creating a “string of beads” appearance. Less commonly the stenosis has a smooth tapered appearance. Fibromuscular dysplasia also weakens the vessel wall which predisposes to dissection.
Location
Fibromuscular dysplasia may affect any medium-sized artery in the body and is commonly multifocal and bilateral (up to 60% when involving the renal arteries). Fibromuscular dysplasia usually involves the mid-segment of vessels and spares origins. Some sites are more frequently involved 9:
-
renal arteries(most common): estimated between ~5% (range 4-6%) in the renal arteries7 -
cervicoencephalic arteries (next most common): estimated prevalence ~1.5% (range 0.3-3%)7-
extracranialinternal carotid arteries vertebral arteries
-
iliac arteries-
coeliac trunkandmesenteric arteries -
subclavianandaxillary arteries -
coronary arteries17
Complications
-
spontaneousdissection distal embolisation (of thrombus formed in aneurysm)-
aneurysms-
renal artery aneurysmin ~40% with renal artery fibromuscular dysplasia12 -
intracranial aneurysms+/-subarachnoid haemorrhage
-
arteriovenous fistula
Radiographic features
Arterial imaging with CT angiography, MR angiography and digital subtraction angiography (DSA) may be used to visualise the lesions in fibromuscular dysplasia.
Selective DSA is the gold standard because it allows the visualisation of small or peripheral lesions. The characteristic finding, particularly in the more common medial subtype, is alternating stenoses and dilatations, causing a string of beads appearance 5.
Less commonly in intimal and adventitial types, there is focal concentric, long-segment tubular stenosis or diverticular outpouching present (see carotid intimal fibromuscular dysplasia). Cross-sectional imaging (CT and MRI) allows the assessment of end-organ ischaemic damage.
- typical angiographic features include: vascular loops, fusiform vascular ectasia and a string of beads
- less typical features include: arterial dissection, aneurysm and subarachnoid haemorrhage
Treatment and prognosis
Asymptomatic cases are only observed but if symptomatic then fibromuscular dysplasia responds well to angioplasty, with high long-term patency rates. A stent is generally not required.
Complications
- spontaneous dissection
- distal embolisation (of thrombus formed in aneurysm)
-
aneurysms
- renal artery aneurysm in ~40% with renal artery fibromuscular dysplasia 12
- intracranial aneurysms +/- subarachnoid haemorrhage
- arteriovenous fistula
History and etymology
The first case of fibromuscular dysplasia was initially described by Leadbetter and Burkland in in 1938, while the first case of histologically proven carotid fibromuscular fibromuscular dysplasia was published by M C Connett and J M Lansche in 1965 7.
Differential diagnosis
Imaging differential considerations include:
- atherosclerosis: usually at the origin or proximal portion of the artery
- vasculitides: elevated ESR +/- fever present
- traumatic/iatrogenic vascular injury: correlate with appropriate history
- segmental arterial mediolysis
- vasospasm
-</ul><h4>Pathology</h4><p>The exact cause is not well known. The underlying pathology is a fibrous or fibromuscular thickening of the arterial wall. Any layer of the vessel wall may be affected: intima, media or adventitia. There is an absence of inflammatory cells <sup>1-4,7</sup>.</p><h5>Classification </h5><p>Fibromuscular dysplasia is <a href="/articles/fibromuscular-dysplasia-classification">classified</a> into five categories according to the vessel wall layer affected:</p><ul>-<li>intima: 5% <ul><li>intimal fibroplasia (see <a href="/articles/carotid-web">carotid intimal fibromuscular dysplasia</a>)</li></ul>-</li>-<li>media: 90-95% <ul>-<li>medial dysplasia (70%, commonest type)</li>-<li>perimedial (subadventitial) fibroplasia (15-20%)</li>-<li>medial hyperplasia (8-10%)</li>-</ul>-</li>-<li>adventitia: rare <ul><li>adventitial fibroplasia (1%) <sup>8</sup>-</li></ul>-</li>-</ul><p>The outcome is arterial stenoses. Fibromuscular dysplasia most commonly causes small stenoses along a vessel with intervening areas of dilatation (small aneurysms), creating a “string of beads” appearance. Less commonly the stenosis has a smooth tapered appearance. Fibromuscular dysplasia also weakens the vessel wall which predisposes to dissection.</p><h5>Location</h5><p>Fibromuscular dysplasia may affect any medium-sized artery in the body and is commonly multifocal and bilateral (up to 60% when involving the renal arteries). Fibromuscular dysplasia usually involves the mid-segment of vessels and spares origins. Some sites are more frequently involved <sup>9</sup>:</p><ul>- +</ul><h4>Pathology</h4><p>The exact cause is not well known. The underlying pathology is a fibrous or fibromuscular thickening of the arterial wall. Any layer of the vessel wall may be affected: intima, media or adventitia. There is an absence of inflammatory cells <sup>1-4,7</sup>.</p><h5>Location</h5><p>Fibromuscular dysplasia may affect any medium-sized artery in the body and is commonly multifocal and bilateral (up to 60% when involving the renal arteries). Fibromuscular dysplasia usually involves the mid-segment of vessels and spares origins. Some sites are more frequently involved <sup>9</sup>:</p><ul>
-<a href="/articles/renal-artery">renal arteries</a> (most common): estimated between ~5% (range 4-6%) in the renal arteries <sup>7</sup>- +<a href="/articles/renal-artery">renal arteries</a> (most common): estimated between ~5% (range 4-6%) in the renal arteries <sup>7</sup>
-<a href="/articles/coeliac-artery">coeliac trunk</a> and <a href="/articles/mesenteric-arteries">mesenteric arteries</a>- +<a href="/articles/coeliac-artery">coeliac trunk</a> and <a href="/articles/mesenteric-arteries">mesenteric arteries</a>
-<a href="/articles/subclavian-artery">subclavian</a> and <a href="/articles/axillary-artery">axillary arteries</a>- +<a href="/articles/subclavian-artery">subclavian</a> and <a href="/articles/axillary-artery">axillary arteries</a>
-<a title="Coronary artery" href="/articles/coronary-arteries">c</a><a href="/articles/coronary-arteries">oronary arteries</a><sup>17</sup>- +<a href="/articles/coronary-arteries">c</a><a href="/articles/coronary-arteries">oronary arteries</a> <sup>17</sup>
- +</li>
- +</ul><h5>Classification </h5><p>Fibromuscular dysplasia is <a href="/articles/fibromuscular-dysplasia-classification">classified</a> into five categories according to the vessel wall layer affected:</p><ul>
- +<li>intima: 5% <ul><li>intimal fibroplasia (see <a href="/articles/carotid-web">carotid intimal fibromuscular dysplasia</a>)</li></ul>
- +</li>
- +<li>media: 90-95% <ul>
- +<li>medial dysplasia (70%, commonest type)</li>
- +<li>perimedial (subadventitial) fibroplasia (15-20%)</li>
- +<li>medial hyperplasia (8-10%)</li>
- +</ul>
- +</li>
- +<li>adventitia: rare <ul><li>adventitial fibroplasia (1%) <sup>8</sup>
- +</li></ul>
- +</li>
- +</ul><p>The outcome is arterial stenoses. Fibromuscular dysplasia most commonly causes small stenoses along a vessel with intervening areas of dilatation (small aneurysms), creating a “string of beads” appearance. Less commonly the stenosis has a smooth tapered appearance. Fibromuscular dysplasia also weakens the vessel wall which predisposes to dissection.</p><h4>Radiographic features</h4><p>Arterial imaging with CT angiography, MR angiography and digital subtraction angiography (DSA) may be used to visualise the lesions in fibromuscular dysplasia. </p><p>Selective DSA is the gold standard because it allows the visualisation of small or peripheral lesions. The characteristic finding, particularly in the more common medial subtype, is alternating stenoses and dilatations, causing a <a href="/articles/string-of-beads-sign-renal-artery-1">string of beads</a> appearance <sup>5</sup>. </p><p>Less commonly in intimal and adventitial types, there is focal concentric, long-segment tubular stenosis or diverticular outpouching present (see <a href="/articles/carotid-web">carotid intimal fibromuscular dysplasia</a>). Cross-sectional imaging (CT and MRI) allows the assessment of end-organ ischaemic damage.</p><ul>
- +<li>typical angiographic features include: vascular loops, fusiform vascular ectasia and a string of beads</li>
- +<li>less typical features include: arterial dissection, aneurysm and <a href="/articles/subarachnoid-haemorrhage">subarachnoid haemorrhage</a>
-</ul><h5>Complications</h5><ul>- +</ul><h4>Treatment and prognosis</h4><p>Asymptomatic cases are only observed but if symptomatic then fibromuscular dysplasia responds well to angioplasty, with high long-term patency rates. A stent is generally not required.</p><h5>Complications</h5><ul>
-<a href="/articles/renal-artery-aneurysm">renal artery aneurysm</a> in ~40% with renal artery fibromuscular dysplasia <sup>12</sup>- +<a href="/articles/renal-artery-aneurysm">renal artery aneurysm</a> in ~40% with renal artery fibromuscular dysplasia <sup>12</sup>
-<a href="/articles/saccular-cerebral-aneurysm">intracranial aneurysms</a> +/- <a href="/articles/subarachnoid-haemorrhage">subarachnoid haemorrhage</a>- +<a href="/articles/saccular-cerebral-aneurysm">intracranial aneurysms</a> +/- <a href="/articles/subarachnoid-haemorrhage">subarachnoid haemorrhage</a>
-</ul><h4>Radiographic features</h4><p>Arterial imaging with CT angiography, MR angiography and digital subtraction angiography (DSA) may be used to visualise the lesions in fibromuscular dysplasia. </p><p>Selective DSA is the gold standard because it allows the visualisation of small or peripheral lesions. The characteristic finding, particularly in the more common medial subtype, is alternating stenoses and dilatations, causing a <a href="/articles/string-of-beads-sign-renal-artery-1">string of beads</a> appearance <sup>5</sup>. </p><p>Less commonly in intimal and adventitial types, there is focal concentric, long-segment tubular stenosis or diverticular outpouching present (see <a href="/articles/carotid-web">carotid intimal fibromuscular dysplasia</a>). Cross-sectional imaging (CT and MRI) allows the assessment of end-organ ischaemic damage.</p><ul>-<li>typical angiographic features include: vascular loops, fusiform vascular ectasia and a string of beads</li>-<li>less typical features include: arterial dissection, aneurysm and <a href="/articles/subarachnoid-haemorrhage">subarachnoid haemorrhage</a>-</li>-</ul><h4>Treatment and prognosis</h4><p>Asymptomatic cases are only observed but if symptomatic then fibromuscular dysplasia responds well to angioplasty, with high long-term patency rates. A stent is generally not required. </p><h4>History and etymology</h4><p>The first case of fibromuscular dysplasia was initially described by <strong>Leadbetter</strong> and <strong>Burkland</strong> in 1938, while the first case of histologically proven <em>carotid</em> fibromuscular dysplasia was published by <strong>M C Connett </strong>and <strong>J M Lansche</strong> in 1965 <sup>7</sup>.</p><h4>Differential diagnosis</h4><p>Imaging differential considerations include:</p><ul>- +</ul><h4>History and etymology</h4><p>The first case of fibromuscular dysplasia was initially described by Leadbetter and Burkland in 1938, while the first case of histologically proven carotid fibromuscular dysplasia was published by M C Connett and J M Lansche in 1965 <sup>7</sup>.</p><h4>Differential diagnosis</h4><p>Imaging differential considerations include:</p><ul>