Transcatheter coil or medical glue embolization is one of the most effective treatment options for various bleeding complications that may occur during various transcatheter procedures, such as coronary artery catheterization and bleeding that occur during percutaneous nephrolithotomy (PCNL) treatment. Various other materials that could be used in embolization include coils, ethanol, sodium tetradecyl sulfate, cyanoacrylate, polyvinyl alcohol, microspheres, and gelatin sponge (Gelfoam), among others. Embolic agents are either temporary or permanent. Permanent agents are more common, and there are many applicable subsets, including liquid agents, particulates, coils, and detachable plugs and balloons (Figure 1).
Catheter embolization can be applied to almost any part of the body to control or prevent abnormal bleeding due to several causes (1). Some common problems that are treated using catheter embolization include:
Given the versatility of the embolization procedure, Ari et al. (2) utilized the subcutaneous fat tissue taken with the subcutaneous fascia from the femoral site to stop the bleeding complication from the PCNL. Using this subcutaneous fat tissue embolization method, the authors could successfully stop the bleeding in two patients. In addition, they demonstrated that the treatment option was safe and reliable for PCNL (2). The advantages of the technique used by the authors are that the embolization could be achieved quickly without the guidewire ever being moved, and the technique seems to be quickly employed to embolize the bleeding point rapidly. The risk of infection and an allergic reaction is likely to be low because it uses autologous subcutaneous tissue. Furthermore, this technique is inexpensive since it does not require any extra material regarding the materials needed to implement the technique.
In this context, it is noteworthy that a similar technique was used to block only the tumor feeding vessels that resulted in the regression of the hepatoma, a giant cell tumor of the bone, and renal cell carcinoma (3,4). In this technique, we used the lithium salt of gamma-linolenic acid (GLA, 18;3 n-6), a small molecular weight lipid that has been conjugated to an iodized salt solution that is radio-opaque. This new molecule, called LGIOC (Lithium-gamma-linolenic acid conjugated to an oily lymphographic agent), when injected close to the tumor feeding vessel completely blocked all the tumor feeding vessels without any effect on normal blood vessels (Figures 2, 3). In this instance, the gamma-linolenic acid used is also a lipid (fat) but is different from the subcutaneous fat used by Ari et al. (2). It is possible that the subcutaneous fat used by Ari et al. (2) also contains some amount of gamma-linolenic acid, but this needs to be confirmed by further analysis. In general, subcutaneous fat is a mixture of several lipids, such as cholesterol, triglycerides, saturated and unsaturated fats, and other lipids. Exactly how the subcutaneous fat used by Ari et al. (2) and LGIOC employed by us can block the blood supply is not clear.
In general, when cytotoxic drugs are infused, they would cause vasospasticity leading to vasospasm that is of short duration: 24-48 hours. In our study (3,4), the occlusion of tumor-feeding vessels after the infusion of LGIOC lasted for more than 7-10 days and, in one of our patients, the occlusion of the tumor-feeding vessels lasted for more than three months, and in another, for more than 15 years suggesting that the occlusion of the vessels is almost permanent. It is possible that GLA-induced free radical generation (5,6) acts on endothelial cells of the tumor-feeding vessels and induces their occlusion and thus, produces their anti-angiogenic and anti-vascular actions. Of more than 170 transcripts expressed in the endothelium, 70 were differentially expressed, including 46 that were specifically increased in tumor-associated endothelium (7), suggesting that there are significant differences in gene expression profiles in endothelium derived from normal and tumor vessels. It is possible that LGIOC [and possibly, the subcutaneous fat tissue used by Ari et al. (2)] can stimulate some of the genes and/or receptors in the endothelium of the tumor blood vessels, which may have a role in the occlusion of the tumor vessels observed in our study.
Thus, there is seems to be a significant role for subcutaneous fat and LGIOC and similar lipids in specifically occluding abnormal vessels (tumor feeding vessels, arterio-venous malformations, or vessels that rupture and bleed during some procedures). It is possible that these abnormal vessels are weak at these bleeding spots because of abnormalities in the endothelium and vessel wall that could be exploited for therapeutic purposes.