- Case report
- Open Access
Cystic adventitial disease of the popliteal artery: features on 3T cardiovascular magnetic resonance
© Tomasian et al; licensee BioMed Central Ltd. 2008
- Received: 25 April 2008
- Accepted: 13 August 2008
- Published: 13 August 2008
Cystic adventitial disease (CAD) of the popliteal artery is a rare vascular disease of unknown etiology in which a mucin-containing cyst develops in the adventitial layer of the artery. We report the case of a 26-year-old male with CAD of the right popliteal artery diagnosed non-invasively with 3 Tesla cardiovascular magnetic resonance and confirmed on post-operative histopathology.
- Cardiovascular Magnetic Resonance
- Popliteal Artery
- Intermittent Claudication
- Adventitial Layer
- Maximum Walk Distance
Cystic adventitial disease (CyAD) is a rare non-atherosclerotic condition which results in intermittent claudication due to peripheral vascular insufficiency caused by compression of the arterial lumen by a cystic collection of mucinous material containing varying combination of mucopolysaccharides and mucoproteins within the adventitial layer of the artery. The disease predominantly affects the popliteal artery (85% of cases), typically in young to middle-aged men with a male-to-female ratio of 15:1 . The etiology of CyAD remains controversial . Recent advances in cross-sectional imaging have made possible non-invasive diagnosis of this disease using computer tomography (CT) or cardiovascular magnetic resonance (CMR) [2, 3].
Imaging Sequences and Parameters for Cardiovascular Magnetic Resonance
Slice thickness (mm)
T1-weighted Spin-echo (axial plane)
T2-weighted Turbo Spin-echo (axial plane)
T1-weighted post-contrast fat saturated two-dimensional gradient echo (GRE) (axial and coronal planes)
CE-MRA: three dimensional fast GRE*
The patient returned to full activity in one week, and remained asymptomatic during the 20-month follow-up period.
The most common non-atherosclerotic diseases of the popliteal artery include thrombosed aneurysm, embolism, entrapment syndrome, and CyAD . The incidence of CyAD is estimated to be 1 in 1200 cases of claudication , with cases described involving external iliac, femoral, popliteal, radial, and ulnar arteries and veins [2–5]. The symptoms usually include progressive claudication of the lower extremities with no significant evidence of atherosclerotic disease, and although CyAD usually presents in middle-aged patients , a few reports exist featuring this condition in other ages [6, 7]. The etiology of CyAD is unclear, and the proposed hypotheses include repetitive trauma to the adventitia caused by flexion injuries leading to cystic degeneration, embryological origin, direct communication with the herniated synovial structures of the adjacent joint, and CyAD as a part of a connective tissue disease . Slow progression of CyAD over a period of several years accounts for masslike appearance and large size of the most lesions .
As an inexpensive and readily available diagnostic modality, ultrasound demonstrates anechoic or hypoechoic cystic lesions on gray-scale images, and intra-arterial sonogram reveals adventitial origin of the lesion . Although regarded as the gold standard, conventional angiography has disadvantages such as invasiveness, and exposure to radiation and nephrotoxic contrast agents, and is only diagnostic when characteristic findings such as scimitar (eccentric compression) or hourglass (concentric compression) signs are present . CT and CMR are excellent non-invasive diagnostic modalities for accurate characterization of the cystic lesions and their anatomical relationship to vascular structures [2, 3, 9]. Contrast enhanced CT may demonstrate CyAD as a non-enhancing cystic mass extrinsically compressing the enhancing crescentic arterial lumen .
The introduction of 3T MR systems, with higher inherent signal-to-noise ratio compared to lower field strength scanners, has resulted in improved spatial resolution and faster data acquisition, and with the heightened signal sensitivity to gadolinium-based contrast agents at 3T, high resolution CE-MRA can be performed with low dose contrast protocols, further improving non-invasive assessment of vascular diseases.
The CMR features of CyAD are quite characteristic, and the anatomical extent of the arterial intramural cystic lesions are demonstrated using multi-planar data acquisitions. Individual cysts typically show homogeneous low signal intensity on T1-weighted Spin-echo, and high signal intensity on T2-weighted Turbo Spin-echo images , as described in our case. On post-contrast T1-weighted GRE images the non-enhancing hypo-intense intramural cysts with smooth extrinsic compression of the adjacent arterial lumen are clearly depicted. However, since the underlying pathophysiology leads to myxoid degeneration , lesions may demonstrate enhancement as seen in other myxoid processes. High resolution CE-MRA at 3T is a robust technique for accurate assessment of degree and length of the arterial stenosis or occlusion while depicting lack of significant atherosclerotic process in other arteries of the extremities in CyAD, and may alleviate the need for invasive catheter angiography. Since CyAD may be bilateral, it is important to image both legs. Follow up imaging with CE-MRA or high resolution ultrasound may be performed to look for recurrence or any residual disease.
Surgical treatment options to restore popliteal arterial flow include resection of the affected artery and interposition grafting , aspiration of cystic contents , and resectional adventitial cystotomy .
Utilizing various high resolution image acquisition sequences in multiple orientations combined with CE-MRA at 3T, CMR has an important role for non-invasive morphological assessment, tissue characterization, and vascular evaluation in cystic adventitial disease.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
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