Late T2EL arising from IIA may occur after EVAR for aortoiliac aneurysm up to 16% through five years after the first procedure [
1]. Nearly half of patients show aneurysmal sac growth and need intervention to avoid rupture. According to Werner Gibbins [
6] secondary type II endoleaks are often the result of flow through patent iliolumbar or sacral artery collaterals that normally are little branches hardly visible during conventional angiography due to parallax effect. In support of this contention, a retrospective analysis over 53 procedures by Heye [
7], conducted to evaluate whether T2EL is more frequent in case of antegrade residual flown versus total occlusion after coil embolization of IIA, demonstrated the same incidence of T2EL in both conditions and concluded that complete occlusion of the target vessel at the end of the procedure is not necessary to prevent type II endoleak after endograft placement for aortic or iliac aneurismatic disease but pointed out that in all cases in which an endoleak was detected, a patent iliolumbar artery at the origin of the hypogastric artery was present causing retrograde flow. That is the reason why several authors suggest identifying and occlude the iliolumbar artery when performing IIA embolization to avoid its retrograde flow with endoleak development during the follow-up [
8,
9]. Other factors influencing endoleak appearance are number and diameter of lumbar arteries and some authors suggest their embolization in selected cases[
10]. Alternative causes may be the hypertrophy of vasa vasorum induced by the hypoxic environment in the arterial wall after covered stents deployment or inflammatory processes generated by the thrombus derived contents as explained by Patel and Fikani[
11,
12]. Despite their origin, T2EL from IIA true natural history is uncertain. They often resolve spontaneously but in half of cases endoleak may persist causing sac enlargement1,[
13]. This occurrence may be a risk condition and reported iliac rupture cases during conservative management and poor results after emergency treatment suggest elective approach[
14]. Specific guidelines are absent, but there is agreement about treatment if the sac has expanded >1 cm over the last year or if 5 mm expansion between two examinations was documented[
15]. Past management consisted in open surgery with ligation of internal iliac artery, but nowadays lesser invasive procedures exist so current strategy reserves traditional surgery as a second option in suitable patients. Literature provides several treatment options suitable for different conditions and a narrative review of relevant articles about type II endoleak from IIA after EVAR was conducted to provide a summary of relevant treatment options. Aiming to reduce morbidity, laparoscopic aortic aneurysm repair has been proposed since 2001 [
16]. Even they re-intervention were treated with the same technique and a laparoscopic endoleak treatment was described by Zou et al. [
17] in a particular case of type II endoleak of both inferior mesenteric artery and internal iliac artery causing abdominal aneurysmal sac enlargement and pain. It allowed the concomitant treatment of the two endoleak at the same procedure in a relatively short time. But the technical difficulty and the poor reproducibility of the procedure limited the spread among vascular surgeons. In recent years the endovascular approach has advanced as the first choice. The endovascular goal is to interrupt the nidus flow by filling the nidus itself and embolize feeding vessels in order to relieve aneurysmal sac pressure. It is not always possible achieve the two targets and often procedures end when one of the two has been realized. Several studies dealing with T2EL treatment focused on the relative contribution of the two targets but failed to clarify whether sac embolization alone is better than feeding vessels occlusion [
7]. This aspect can be explained by difficulty in revealing or reaching small collaterals vessels or anatomic variant. Afterall, this review did not evidence any difference regarding short-term result in terms of sac enlargement, freedom from recurrence of EL and reinterventions between the two techniques; furthermore, the only case of post procedural ischemic complication (buttock claudication) was observed after feeding vessel embolization (
Table 1) and that is the reason why san embolization may be deemed sufficient. In our case endoleak source was unknown since the angiography demonstrated that the previous IIA plug had not dislocated and both common and external artery had been previously covered. So, our objective was the obliteration of the nidus itself. The endovascular route was challenging as coverage of EIA precluded direct IIA access. In these cases, different ways are feasible. Direct anterior percutaneous trans-iliopsoas sac puncture has been described [
18]. It has the potential benefit of directly reaching the nidus of the endoleak but requires no vital structures like bowel loops between the aneurysmal sac and puncture site. Since patient motion can influence advancement of the needle, general anaesthesia is required but the major disadvantage is transferring the patient between the angio-suite and the CT scanner that increases operative time including the risk of dislocation of the needle. Cone beam CT can reduce operative time, but it is not available in all angio suites. A transosseous pelvic posterior CT guided approach is described as an alternative to the anterior one when a safe route which prevents lesions of vital structures is not present and it is chosen as the shortest, safest route into the aneurysm that avoids bowel’s loop19. Possible complications of this technique include osteomyelitis, retroperitoneal haemorrhage, and fracture of the bone being transgressed. Considering the invasiveness of this procedure, it can be performed when no anterior ways are eligible and an absolute contraindication about use of contrast iodine medium is present like increased creatinine levels or allergy has been shown by the patient. The transealing technique described by Coppi et al. [
20] is a reliable option in which the nidus of the endoleak is reached through the virtual space between the arterial wall and represents a feasible and safe alternative in selected patients with T2El suppling aortic aneurismal sac. Unfortunately, it can only be applied safely when the graft lands on the common iliac artery. Otherwise, when the endograft lands on the external iliac artery this technique is ineligible owing to the smaller caliber of the vessel and risk of rupture or dissection. A different strategy can be used in chronic obstructive arterial disease in which multiple collateral pathways that dilate during time are observed and the transcatheter arterial approach via the deep femoral artery collateral pathways linking to the internal iliac artery circulation has been used [
21] but it is technically demanding due to the complexity of the collateral pathway itself if present. In our case, direct puncture of the aneurysm was avoided since its anatomical features as well as the posterior approach for seronegative polyarthritis presented by the patient exposing for bone fracture. So, we decided for a superior gluteal approach. Embolization through retrograde, direct SGA access can solve all these issues as it allows a closer way to reach the target vessel without entering the peritoneal cavity or crossing the iliac bone eliminating associated risks. This approach has already been reported in recent years and during the literature review process we found 9 papers that utilized the same way for an overall amount of 10 patients4,6, [
10,
22,
23,
24,
25,
26,
27]. Direct surgical exposure or CT guided puncture of the SGA could have been an alternative4, [
28], but both fluoroscopic roadmapping and sonographic guidance provided a good visualisation of the target vessel allowing its puncture with a mini-invasive approach. Small or calcified target vessels can make difficult the endovascular access, but angiography excluded such a situation in our case. Anyway, multiple imaging supporting modalities are required and CT-guidance, DUS-guidance, and fluoroscopic-guidance alone or, most often, in combination are necessary. We too resorted to the combination of fluoroscopic and DUS-guidance. An innovative modality has been recently described by Chi et al who utilized a 18-gauge (7-cm) SMART Doppler ultrasound-guided needle vascular access device (Vascular Solutions, Minneapolis, Minn) to directly access the SGA24. At the end of the procedure, issues for access site hemostasis achievement raise since deep location of SGA and absence of bony structures to compress against. Embolization of the access site has been proposed [
27] but the potential risk is represented by distal ischaemia. Alternatively, off-label use of arterial closure devices such as StarClose or Angio-Seal [
24,
26] can be utilized, but correct deployment of closure devices may be difficult when the target artery has a deep location and may require surgical exposure. Our strategy consisted of sheathless low-profile devices that made the arteriotomy very small. Furthermore, heparin neutralization at the end of the procedure made manual compression successful. One aspect that was never considered in any of the studies examined in this specific setting of endoleak arising from the internal iliac artery was the use of anticoagulants. However, there have been several studies comparing type II endoleak occurrence with abdominal aneurismal sac perfusion in patients treated with anticoagulation versus antiplatelet therapy alone. The first study postulating that anticoagulation can be an important factor influencing failure after endoluminal graft treatment was a case report by Torsello et al. [
29] that reported a case of aneurysm rupture 16 months after a successful EVAR in a patient on coumadin due to atrial fibrillation. Even if no endoleak was detected at scheduled CT scan, aneurismal sac enlargement was noted before rupture and after emergency treatment the presence of thrombus in the proximal neck and the concomitant anticoagulant therapy were recognized as possible factors for endograft failure. But the biggest study evaluating long-term impact of anticoagulation on late endoleak occurrence after EVAR is that of Flohr et al. [
30] that over a retrospective cohort of 29,783 patients found that late endoleaks were more common in patients treated with anticoagulation after EVAR.