Focal intramural hematoma as a potential pitfall for iatrogenic aortic dissection during subclavian artery stenting: A case report

Abstract

BACKGROUND

Iatrogenic aortic dissection (IAD) is a rare but fatal complication of interventional treatment for the proximal supra-aortic large vessels. Several cases of IAD after endovascular treatment of subclavian artery have been reported. Nevertheless, the pathogenesis of IAD is still unclear. Here we report a patient with IAD following a balloon expandable stent implanted into the left subclavian artery (LSA).

CASE SUMMARY

An 84-year-old man with a history of hypertension was admitted to the Neurology Department of our hospital complaining of dizziness and gait disturbance for more than 1 mo. Computed tomography angiography of the head and neck showed severe stenosis at the proximal LSA and the origin of the left vertebral artery. Magnetic resonance diffusion-weighted imaging of the brain revealed subacute infarctions in cerebellum, occipital lobe and medulla oblongata. He suffered a Stanford type B aortic dissection after the proximal LSA angioplasty with a balloon expandable stent. Thoracic endovascular aortic repair was performed immediately with the chimney technique and he was discharged 20 d later. After exploring the pathogenesis with multimodal imaging analysis, an easily neglected focal intramural hematoma (IMH) in the aorta near the junction of the LSA was found to be the main cause of the IAD. The risk of IAD should be sufficiently evaluated according to the characteristics of aortic arch lesions before the proximal LSA angioplasty.

CONCLUSION

Focal aortic IMH is a potential risk factor for IAD during a seemingly simple stenting of the proximal LSA.

Key Words: Intramural hematoma, Subclavian artery stenting, Iatrogenic aortic dissection, Case report

Core Tip: Iatrogenic aortic dissection (IAD) is a rare complication during angioplasty or stenting for the proximal left subclavian artery (LSA) stenosis. The authors present an 84-year-old patient with posterior circulation stroke who suffered an aortic dissection immediately after proximal LSA stenting and achieved a favorable outcome following active treatment. The easily neglected focal intramural hematoma is a potential risk factor for IAD in this procedure. The characteristics of aortic arch lesions should be sufficiently evaluated with multimodal imaging analysis before the proximal LSA angioplasty to avoid the occurrence of such event.

INTRODUCTION

Subclavian artery stenosis can lead to chronic blood insufficiency of the upper limb or vertebrobasilar system and, in severe cases, to subclavian steal syndrome or posterior circulation ischemic stroke. At present, endovascular stenting is one of the most important interventional treatments for symptomatic atherosclerotic stenosis of the subclavian artery with a certain degree of reliability and safety[1]. However, subclavian artery stenting complicated by iatrogenic aortic dissection (IAD) is a rare and frustrating situation. In this case, we report a patient with IAD following implantation of a balloon expandable stent into the left subclavian artery (LSA) due to a focal aortic intramural hematoma (IMH).

CASE PRESENTATION

Chief complaints

An 84-year-old male was admitted to our department due to dizziness and gait disturbance lasting more than 1 mo.

History of present illness

The patient had a history of hypertension for more than 10 years. Except for age, gender and hypertension, the patient had no other predisposing factors for stroke such as trauma, obesity, diabetes, dyslipidemia, heart disease, atrial fibrillation, smoking, alcohol consumption, drug abuse, asymptomatic carotid stenosis and sleep apnea syndrome.

History of past illness

There was no previous stroke or transient ischemic attack in his history.

Personal and family history

There was no obvious abnormality in his personal and family history.

Physical examination

The blood pressure of the right upper limb was 128/78 mmHg, while that of the left was 113/66 mmHg. The neurological examination revealed the ataxia of right limb, but had no visual field defects and typical clinical symptoms of Wallenberg’s syndrome such as nystagmus, dysphagia, intersectional paresthesia and Horner’s sign.

Imaging examinations

Magnetic resonance (MR) diffusion-weighted imaging and non-contrast computed tomography of the brain revealed subacute infarctions in cerebellar hemisphere, occipital lobe and medulla oblongata after admission (Figure 1A). MR perfusion-weighted imaging also showed that there was no significant difference in relative cerebral blood flow, relative cerebral blood volume, the mean transit time and the time to peak between bilateral cerebellar hemispheres except the infarct core (Figure 1B).

Figure 1 Imaging evaluations of brain before subclavian artery stenting. A: Magnetic resonance (MR) diffusion-weighted imaging and non-contrast computed tomography scan showed the coexistence of acute and subacute infarctions in cerebellum, medulla oblongata and occipital lobe (white arrow); B: MR-perfusion-weighted imaging showed that there was no significant difference in relative cerebral blood flow, relative cerebral blood volume, mean transit time and time to peak between bilateral cerebellar hemispheres except the infarct core; C: Computed tomography angiography showed the calcified plaques lead to the stenosis of proximal left subclavian artery (white arrow), stenosis at origin of the left vertebral artery (VA) (orange arrow), the occlusion of right VA (yellow arrow), and the bilateral posterior communicating arteries were not opening (black arrow point to the top of basilar artery).

Before admission, computed tomography angiography (CTA) of the head and neck had been performed in another hospital, showing total occlusion of the right vertebral artery (VA) and severe stenosis at the proximal LSA and the origin of the left VA. CTA also revealed the bilateral posterior communicating arteries were not opening which means the incomplete Willis circle (Figure 1C).

FINAL DIAGNOSIS

In the review of the interventional procedure, we noticed that a significant motion artifact was displayed on the lateral wall of the descending aorta in the first aortic arch angiogram. Furthermore, the axial views on pre-admission CTA revealed the displacement of aortic intimal calcification near the junction of the LSA (Figure 2A). We also compared the CTA and digital subtraction angiography (DSA) images of two other adult patients and found that the second patient, who had presented with penetrating atherosclerotic ulcers, showed a similar artifact on anteroposterior DSA image (Figure 2B), while the third patient, who had no IMH or ulcers, had no obvious artifact (Figure 2C).

Figure 2 Comparison of aortic arch images between three male patients with anteroposterior views on digital subtraction angiography and axial views on computed tomography angiography. A: Images of this present case showed a significant artifact on lateral wall of descending aorta (white arrow) and displacement of aortic intimal calcification (black arrow); B: Images of the second patient, aged 79-years-old, showed a similar artifact (white arrow) and penetrating atherosclerotic ulcers (black arrow); C: Images of the third patient, aged 64-years-old, showed mild atherosclerosis on the aortic wall without obvious artifact (white arrow).

Based on the above analysis, the final diagnosis of the case is IAD due to a focal aortic IMH.

TREATMENT

After 4 d of intensive therapy with antiplatelet drugs and statins, endovascular stenting for the stenosis of the LSA and left VA origin was scheduled. The right femoral artery access was established under local anesthesia and DSA showed that the vascular lesions were consistent with those on CTA (Figure 3A). A 9 mm × 25 mm balloon expandable stent (Boston Scientific, Galway, Ireland) was subsequently implanted at a pressure of 10 atm into the proximal LSA. Unfortunately, the patient suffered significant chest pain immediately after the stent was released. Subsequent angiography showed contrast entering the aortic wall near the proximal edge of the stent (Figure 3B) and narrowing of the true lumen of the descending aorta, which was considered a Stanford type B aortic dissection (Figure 3C).

Figure 3 The procedures of subclavian artery stenting for stenosis and thoracic endovascular aortic repair for aortic dissection. A: Severe stenosis of the proximal left subclavian artery (LSA) (white arrow) and the ostium of ipsilateral vertebral artery (black arrow) were presented in digital subtraction angiography; B: Contrast entering the aortic wall (white arrow) after a balloon expandable stent implanted into LSA; C: The true lumen and false lumen (FL) could be clearly displayed in angiogram of aortic dissection, and the origin of dissection was identified at the proximal edge of stent; D: Chimney technique was used in thoracic endovascular aortic repair; E: Two-week computed tomography angiography (CTA) follow-up, there was no significant contrast enter into the FL, and the distal end of aortic dissection was at least below the bifurcation point of celiac trunk (white arrow, CTA failed to scan the whole dissection).

The patient was placed under general anesthesia immediately. Left femoral and brachial artery access was established. Considering the high risk of stroke due to severe stenosis of left VA and malperfusion of LSA, we chose the chimney technique to shorten the procedure time. After measuring vascular diameter and length with a calibrated pigtail catheter, a 32 mm × 20 cm thoracic aorta covered stent-graft system (Medtronic Vascular, Santa Rosa, Calif), and another 8 mm × 50 mm covered stent (Viabahn, Cook Medical, Bloomington, IN) was placed in the proximal LSA to maintain blood flow to the left VA and axillary artery (Figure 3D). After these procedures were completed, the contrast was still observed to slowly enter the entrance of the aortic dissection, so two 12 mm × 14 cm and four 10 mm × 14 cm coils (Cook Medical, Bloomington, IN) were deployed near the intimal tear for further embolization.

OUTCOME AND FOLLOW-UP

The patient developed bloody pleural effusion and severe anemia after thoracic endovascular aortic repair. After blood transfusion and pleural effusion drainage, the patient was discharged 20 d later. CTA of the thoracic aorta at the 2-wk follow-up showed complete exclusion of the false aortic lumen, and no endoleak had occurred (Figure 3E). At the 3-mo follow-up over telephone interview, the patient reported no more chest pain, and the symptoms of dizziness and ataxia had been significantly relieved.

DISCUSSION

IAD typically occurs after coronary artery bypass graft, thoracic endovascular aneurysm repair and aortic valve surgery[2]. However, IAD is rarely observed during endovascular treatment of the proximal supra-aortic arch vessels such as the subclavian artery and brachiocephalic trunk. Although several cases which related to IAD after LSA stenting, balloon angioplasty and occlusion recanalization have been reported in the scientific literature, the pathogenesis is still unclear[3-5]. There are opinions suggesting that severe aortic calcification or atherosclerosis may be the cause of IAD after interventional treatment[3,6].

In the present case, CTA showed that the stenosis of the proximal LSA was associated with calcified plaque, but the degree of calcification of the aortic arch was not high. One prominent sign on axial view CTA of the aortic arch was the inward displacement of aortic intimal calcification near the junction of the LSA, which is an important characteristic of both IMH and aortic dissection[7]. CTA also showed no obvious two-lumen flow and crescent-shaped aortic wall thickening. Besides, the patient had no symptoms of chest and back before the intervention procedure, so it was most likely to be considered a focal asymptomatic IMH rather than an aortic dissection. It is noteworthy that IMH may progress to aortic dissection under certain conditions[8]. After the balloon expandable stent was implanted into the proximal LSA in this case, the mechanical squeeze on the IMH may have resulted in intimal layer rupture and subsequent progression to a type B aortic dissection. Furthermore, on anteroposterior aortic arch DSA images, another suspicious sign is an obvious motion artifact on the lateral wall of the descending aorta. We compared the DSA images of two other male patients who had been examined with the same imaging device and found that the artifacts of the descending aorta seemed to be associated with the severity of the aortic wall lesions. However, considering the differences in respiratory rate, heart rate, blood pressure and degree of cooperation among three patients may also affect the occurrence of aortic artifacts, studies with larger sample sizes are needed to further confirm this hypothesis.

Several lessons should be noted in the treatment of this case. First, possible peri-procedural complications such as subclavian artery dissection or rupture, stent thrombosis, stroke and embolism of distal upper limb artery were considered before LSA stenting. Nevertheless, CTA and DSA should be combined to observe the aortic wall near the ostium of the LSA to exclude IMH, penetrating atherosclerotic ulcers or other lesions to comprehensively evaluate the interventional risk of IAD. In addition, the calibrated pigtail catheter was more accurate than the guiding catheter in the measurement of the LSA diameter (8 mm vs 9 mm in this case). A balloon expandable stent with larger diameter can increase compression on the vessel wall, which may lead to a higher risk of IAD. Finally, transradial access could have been considered for angioplasty of the left VA without treatment of the LSA stenosis in this case.

CONCLUSION

Focal aortic IMH is a potential risk factor for IAD during a seemingly simple stenting of the proximal LSA. Sufficient evaluation of multimodal imaging should be performed before the interventional procedures to avoid the occurrence of such event.