Aortic intimal intussusception during acute type B aortic dissection endovascular repair
Introduction
Since the first autopsy reported in 1887 (1), more than 80 cases of aortic intimal intussusception (AoII) have been reported in English-written literatures. AoII is a rare and potential life-threatening disease (2). It is usually secondary to aortic dissection and is developed by the detached intima from its origin (3). Once formed, it can cause malperfusion, posing a great threat to life. However, it is seldom reported during the thoracic endovascular repair (TEVAR) of uncomplicated type B aortic dissection (3). Here we report a case of AoII with malperfusion to raise the awareness of AoII during endovascular repair of aortic dissection.
Case presentation
A 47-year-old man was diagnosed with acute type B aortic dissection in local hospital, complaining of chest and back pain for 4 days (Figure 1). He smoked for 20 years, without other medical history. He was performed of TEVAR in local hospital. After releasing the thoracic aortic stent, no signs of blood flow was observed in the abdominal aortic branches distal to the celiac trunk. Another aortic stent was inserted to recanalize the abdominal aorta, which was occluded by AoII, but finally failed.
The patient was immediately transferred to our hospital, complaining of cold in bilateral lower extremities and back pain, but of no chest or abdominal pain. Physical examination revealed no pulse in bilateral femoral and femoral beyond arteries, along with subnormal skin temperature in bilateral lower extremities. The blood pressure was 190/110 mmHg. The heart rate was 100 per minute and the SPO2% was 93%. Imaging examination confirmed the AoII and also showed thrombus in the abdominal aortic stent (Figure 2A). Occlusions or stenosis happened in the celiac trunk ostium, superior mesenteric artery (Figure 2B) and iliac arteries. Bilateral renal arteries were supplied by the false lumen (Figure 2C,D). The levels of alanine transaminase (ALT), aspartate transaminase (AST), creatinine kinase (CK) and creatinine were separately 370 U/L, 648 U/L, 1,294 U/L and 107 mmol/L. AoII and malperfusion were then diagnosed.
With the patient’s and his family’s consent, hybrid surgeries were applied after multidisciplinary discussion. Open surgery was performed to remove the intussuscepted aortic intima. When the abdominal cavity was exposed, the color of liver showed negative and the intestine peristalsis was inactive, as well as the pulse of mesenteric arteries. Abdominal aorta endarterectomy was applied to take out the failed abdominal aortic stent and to reconstruct the abdominal aorta and its branches (Figure 3). After aorta reconstruction, the intestine returned viable and the mesenteric arteries pulsated again. Endovascular repair was then performed in bilateral iliac arteries and stents were placed. Final angiography showed patency and no leakage of the aorta. Finally, bilateral femoral arteries and dorsal arteries pulsated again. During the operation, no transfusion was needed.
After operation, the patient was transferred to the intensive care unit, where he received mechanical ventilation and controlled blood pressure for 2 days. His postoperative period was uneventful. The creatinine decreased from 107 mmol/L at admission to 65 mmol/L at discharge. The computed tomography angiography (CTA) of the 8th postoperative day showed patent in the aorta and no complications happened (Figure 4). He was discharged on the 8th postoperative day. And blood pressure was monitored at home with routine antihypertensive drugs. No complications happened during the 6th month follow-up (Figure 5).
Discussion
TEVAR has been the main current in dealing with the acute uncomplicated type B dissection. TEVAR-related mortality risk should be assessed before the operation (4). Many TEVAR-related complications are already known among vascular surgeons, such as spinal cord ischemia, etc. But TEVAR-related AoII is seldom reported (3). AoII is usually secondary to aortic dissection. It is mostly reported in type A aortic dissection, with few (1) in type B aortic dissection. Similar to other TEVAR-related AoII cases (3,5,6), this patient also suffered AoII during the endovascular repair of uncomplicated type B aortic dissection. His intima may be torn by a strong radial force after the releasing of thoracic aortic stent, resulting in occlusion of abdominal aorta and no signs of blood flow.
AoII manifests differently based on the locations and the intussusception degree. For the AoII that locates in ascending aorta, the detached intima may fold back into the left ventricular outflow tract (7), leading to aortic regurgitation and the subsequent complications. It may also cause occlusions in the three main branches of arch, which may lead to stroke. While for those in type B aortic dissection, malperfusion may happen if the intima is intussuscepted to a large extent.
AoII can be detected by different imaging methods, such as computed tomography, echocardiogram and magnetic resonance (1). In this case, AoII was detected during the operation by digital subtraction angiography. When the patient was transferred to our hospital, another CTA was performed and further confirmed the lesion.
Methods to deal with the TEVAR-related AoII in descending aorta include immediate conversion to open surgery, percutaneous balloon fenestration and aspiration thrombectomy, etc. In this case, though local doctors tried to recanalize the abdominal aorta by fenestration with another aortic stent, the patient’s situation didn’t get better. Advanced aortic endovascular repair techniques may be helpful, such as parallel grafts. However, within the advanced endovascular techniques, it is difficult to establish a pathway between the aorta and the aortic stent. Besides, several parallel stents are needed to reconstruct the four visceral arteries, which may lead to dissatisfied patency. Another challenge is that this patient suffered abdominal malperfusion, which needed to be dealt with as soon as possible. Considering these factors, we decided to reconstruct the abdominal aorta and the branches by open surgeries. To minimize the wound, we adopted endovascular repair in bilateral iliac arteries. Though the results of 6th month follow-up showed good, with no aorta rupture and no death, long-term follow up is still required.
Conclusions
AoII is rare, especially during the endovascular aortic repair of acute uncomplicated type B aortic dissection. Awareness of AoII should be raised and aorta endarterectomy in time can be life-saving.
Acknowledgments
Funding: Prof. Dr. YJ Li is funded by National Natural Science Foundation of China (No. 81870351), CAMS Innovation Fund for Medical Sciences (CIFMS, 2018-I2M-1-002) and Beijing Hospital Clinical Research 121 Project (No. BJ-2018-089). Dr. YP Diao is supported by the Fundamental Research Funds for the Central Universities (No. 3332018174) and by Beijing Natural Science Foundation (No. 7192186).
Footnote
Conflicts of Interest: The authors have no conflicts of interest to declare.
Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. Written informed consent was obtained from the patient and his family.
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