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DOI:10.2214/AJR.05.0750
AJR 2007; 189:W146-W149
© American Roentgen Ray Society


Case Report

Multiple-Electrode Radiofrequency Ablation of Symptomatic Hepatic Cavernous Hemangioma

J. Louis Hinshaw1, Paul J. Laeseke1, Sharon M. Weber2 and Fred T. Lee, Jr.1

1 Department of Radiology, University of Wisconsin, 600 Highland Ave., E3/311 CSC, Madison, WI 53792.
2 Department of Surgery, University of Wisconsin, Madison, WI.

Received May 2, 2005; accepted after revision August 3, 2005.

 
Address correspondence to F. T. Lee, Jr.

WEB This is a Web exclusive article.

Keywords: cavernous hemangioma • liver • radiofrequency ablation


Introduction
Top
Introduction
Case Report
Discussion
References
 
Hepatic cavernous hemangioma is a common benign neoplasm of the liver present in as many as 20% of bodies at autopsy [1]. Hemangioma generally has a benign course and rarely necessitates intervention of any kind. Some hemangiomas, however, are symptomatic and can cause hepatic hemorrhage, thrombocytopenia, and jaundice [2]. Current medical therapy for symptomatic hemangioma is largely ineffective, and surgical removal, although effective, is associated with high morbidity [3-5]. We describe the use of radiofrequency ablation in the minimally invasive management of a large symptomatic hepatic hemangioma. When this article was first submitted to and accepted for publication, it was the first to describe use of a multiple-electrode radiofrequency ablation system based on a switching algorithm in treatment of a tumor in a human [6].


Case Report
Top
Introduction
Case Report
Discussion
References
 
A 48-year-old man presented with a history of multiple hepatic hemangiomas. The dominant tumor, located in the peripheral right lobe of the liver, had grown from 3.0 to 7.5 cm over the course of 9 years (Fig. 1A). Over that time, the patient had experienced worsening right upper quadrant pain exacerbated by exertion. The patient had thoroughly investigated treatment options before presentation and had refused surgery on several occasions. Because of the large size of the tumor, radiofrequency ablation with standard single-electrode techniques would have required prolonged treatment and anesthesia time, and the decision was made to manage the tumor with a new multiple-electrode radiofrequency switching controller (Cool-tip, Valleylab). This system is based on switching between electrodes at each impedance spike (a rapid increase in impedance greater than 30 ohms) or at a 30-second default setting. Compared with a conventional single-electrode radiofrequency system, the multiple-electrode device increases the duty cycle of the generator by powering additional electrodes during the off time inherent in the standard pulsing algorithm [7]. Because tissue cooling after radiofrequency ablation is slow compared with heating, large thermal lesions can be made when the electrodes are placed in proximity to one other.


Figure 1
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Fig. 1A —48-year-old man with hepatic hemangioma. Contrast-enhanced CT scan in portal venous phase before ablation shows characteristic peripheral nodular enhancement within large hemangioma in right lobe of liver. Delayed images showed areas of enhancement with centripetal filling.

 
In this case, the hemangioma was managed with percutaneous CT and sonographically guided multiple-electrode radiofrequency ablation. The patient was given general anesthesia and placed in the left posterior oblique position on the CT table. Because of the peripheral location of the tumor in direct contact with the diaphragm, 1,000 mL of 5% dextrose in water was infused into the peritoneal space. This technique is routinely used at our institution to protect perihepatic structures in the management of peripheral liver tumors [8, 9]. Under sonographic guidance, three 4.0-cm exposure single electrodes (Cool-tip, Valleylab) were positioned in a triangular array within the center of the hemangioma (Figs. 1B, 1C and 1D). A 16-minute ablation cycle was performed with the switching controller under sonographic guidance. A zone of decreased echogenicity (presumably due to clotting blood) was initially found in the tumor surrounding the electrodes (Figs. 1E and 1F). Hyperechoic gas bubbles then developed (Fig. 1G). Temperatures greater than 50°C were obtained at each electrode, but the hyperechoic zone did not appear to cover the entire tumor. Therefore, electrodes were repositioned around the superior and inferior peripheries of the tumor, and an additional 24 minutes of ablation were performed. At this point, gas bubbles appeared to cover the entire tumor, and the electrodes were removed by standard track. cauterization with a target temperature of approximately 80°C.


Figure 2
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Fig. 1B —48-year-old man with hepatic hemangioma. B= oblique sagittal, C= oblique coronal, D= oblique axial two-dimensional reconstructions of unenhanced CT scans obtained during ablation show placement of electrodes in triangular array within hemangioma.

 

Figure 3
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Fig. 1C —48-year-old man with hepatic hemangioma. B= oblique sagittal, C= oblique coronal, D= oblique axial two-dimensional reconstructions of unenhanced CT scans obtained during ablation show placement of electrodes in triangular array within hemangioma.

 

Figure 4
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Fig. 1D —48-year-old man with hepatic hemangioma. B= oblique sagittal, C= oblique coronal, D= oblique axial two-dimensional reconstructions of unenhanced CT scans obtained during ablation show placement of electrodes in triangular array within hemangioma.

 

Figure 5
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Fig. 1E —48-year-old man with hepatic hemangioma. Longitudinal sonographic image of right lobe of liver before ablation shows large hyperechoic hemangioma. Because of location of hemangioma, intercostal approach was necessary.

 

Figure 6
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Fig. 1F —48-year-old man with hepatic hemangioma. Longitudinal sonographic image obtained soon after initiation of ablation shows development of hypoechoic region around electrodes that may represent evolving thrombus within vascular spaces of hemangioma.

 

Figure 7
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Fig. 1G —48-year-old man with hepatic hemangioma. Longitudinal sonographic image obtained later in ablation session shows evolution of ablation zone to more typical appearance: gas bubbles infiltrating and obscuring ablated region because of dirty acoustic shadowing.

 


Figure 8
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Fig. 1H —48-year-old man with hepatic hemangioma. Contrast-enhanced CT scan in portal venous phase immediately after ablation shows no enhancement within hemangioma. Intraperitoneal 5% dextrose in water (arrowhead) is routinely used at our institution to protect perihepatic structures in management of peripheral liver tumors.

 
Dynamic contrast-enhanced CT immediately after the procedure showed complete ablation of the hemangioma with no residual enhancement on delayed images and minimal damage to adjacent normal liver (Fig. 1H). The total procedure time, including anesthesia induction, ablation, and CT after ablation was approximately 3 hours.

The patient tolerated the procedure well and was discharged the next day with no significant pain. Mild ileus and a bout of gastrointestinal reflux resolved spontaneously within a few days of the procedure. The patient was fully recovered from the procedure within 2 weeks. Within 2 months he had returned to a normally vigorous lifestyle with complete resolution of the right upper quadrant pain.


Discussion
Top
Introduction
Case Report
Discussion
References
 
Hepatic hemangioma is rarely symptomatic but can be associated with abdominal pain and other poorly localized symptoms. The risk of rupture, although low, increases with tumor size and can be associated with even trivial trauma. In this case, the large hemangioma in the right lobe appeared to cause substantial pain with exertion, decreasing the quality of life of an otherwise highly active person. Surgical management of symptomatic hemangioma involves either partial hepatectomy or enucleation, both of which are associated with substantial recovery time and morbidity. Minimally invasive alternatives, such as percutaneous arterial embolization, radiation therapy, and hepatic artery occlusion, also have been used to manage hemangioma but have not proved uniformly effective [10, 11].

Radiofrequency ablation is a rapidly developing technique for the management of abdominal and thoracic tumors. Extensive experience with percutaneous radiofrequency ablation in the management of malignant hepatic tumors has accumulated worldwide. Although local control rates with a single treatment vary with tumor size, tumor type, and proximity to major hepatic blood vessels, the procedure is widely accepted as safe and well tolerated. For the management of benign tumors such as hemangioma, radiofrequency is a near ideal technology because of the cauterizing effect of tissue heating, the small size of the radiofrequency electrodes (17 gauge), and the lack of a requirement to ablate every malignant cell. In the past, a major issue in adequately managing a 7.5-cm tumor would have been the long treatment time. Multiple consecutive overlapping ablations would have been necessary, each ablation taking 6-12 minutes in ablation time alone. After each ablation, gas bubbles, bleeding, and edema would have limited visualization of tumor margins and electrode placement, making the formation of precisely overlapping ablations increasingly difficult.

We found only one report [12] of an evaluation of the efficacy of percutaneous radiofrequency ablation in the management of hemangioma. Although the results were promising (nine of 12 patients reported partial or complete resolution of symptoms), the study was limited by ablation times as long as 125 minutes (range, 8-125 minutes), although hemangiomas as large as 9.5 cm in diameter (range, 2.5-9.5 cm) were managed. Unfortunately, the reporting of methods and results in the article is imprecise. The three treatment failures were not further classified as to size of hemangioma, patient demographic features, or other factors that might have explained a lack of clinical response. In addition, the technique used to follow symptom relief is not defined, and the degree and time period of symptom relief among patients who responded are unclear. These limitations make it difficult to draw meaningful conclusions, but the promising results support the need for further investigation.

A 2004 case report [13] describes ablation of a 5-cm hemangioma (49 cm3), which necessitated three consecutive ablations with a Cool-tip cluster electrode activated for a total of 36 minutes. Cluster electrodes are composed of three 17-gauge electrodes spaced 5 mm apart in an equilateral triangle. By way of comparison, in our case, using three single Cool-tip electrodes, we ablated a hemangioma with a maximal diameter of 7.5 cm (166 cm3) in 40 minutes. The ability to run three electrodes simultaneously resulted in ablation of 339% more tissue at the cost of only four additional minutes. This finding is consistent with data derived from animal studies in which multiple-electrode ablation with the switching controller improved system performance enough to ablate approximately 200% more volume than with a conventional Cool-tip cluster electrode [6].

To our knowledge, this report is the first description of the treatment of a human by use of multiple-electrode radiofrequency ablation with switching technology. The basic principles of radiofrequency ablation are the same for single- and multiple-electrode systems. In multiple-electrode mode, the system takes advantage of the off time built into the standard pulsing algorithm to power additional electrodes [7]. Each electrode is electrically independent and can be widely spaced for simultaneous creation of multiple ablation zones. The electrodes also can be placed close to one another to create a single large zone of ablation [6]. In creation of a single ablation zone with multiple electrodes, an important consideration is the thermal synergy caused by vascular shielding. This phenomenon can cause disproportionately large zones of ablation that must be taken into account in ablation of tumors close to important structures prone to thermal injury, such as bowel and gallbladder. In this case, peritoneal instillation of 5% dextrose in water helped limit dia-phragmatic damage and decrease pain after the procedure [8]. As the size of ablation zones increases with technologic improvements in radiofrequency systems, methods of preventing collateral damage will become increasingly important to decrease the risk of severe complications.

During ablation, we noticed an unexpected evolution of the sonographic characteristics of the hemangioma. The hypoechoic region that developed around the electrodes early in ablation might have reflected thrombus formation in reaction to damage to the endothelial lining of the tumor or to the direct thrombotic effect of heat deposition. This echo pattern is not typical of malignant tumors managed with radiofrequency. Later in the ablation, hyperechoic gas bubbles formed within the areas of thrombus. The relative lack of damage to the normal surrounding liver also is unusual for radiofrequency ablation of malignant tumors and may reflect the substantial blood flow in normal liver compared with the sluggish flow typical of hemangiomas. The greater flow of blood in a normal liver may protect the organ.

We describe the first, to our knowledge, case of treatment of a human by means of multiple-electrode radiofrequency technology based on switching between electrodes. This system appears to rapidly ablate large volumes of tissue by increasing the duty cycle of the radiofrequency generator and taking advantage of the thermal synergy inherent in multiple-electrode ablation.


References
Top
Introduction
Case Report
Discussion
References
 

  1. Ishak KG, Rabin L. Benign tumors of the liver. Med Clin North Am 1975; 59:995 -1013[Medline]
  2. Gibbs JF, Litwin AM, Kahlenberg MS. Contemporary management of benign liver tumors. Surg Clin North Am2004; 84:463 -480[CrossRef][Medline]
  3. Iyer CP, Stanley P, Mahour GH. Hepatic hemangiomas in infants and children: a review of 30 cases. Am Surg1996; 62:356 -360[Medline]
  4. Kawarada Y, Mizumoto R. Surgical treatment of giant hemangioma of the liver. Am J Surg 1984;148 : 287-291[CrossRef][Medline]
  5. Farges O, Daradkeh S, Bismuth H. Cavernous hemangiomas of the liver: are there any indications for resection? World J Surg 1995; 19:19 -24[CrossRef][Medline]
  6. Lee FT Jr, Haemmerich D, Wright AS, Mahvi DM, Sampson LA, Webster JG. Multiple probe radiofrequency ablation: pilot study in an animal model. J Vasc Interv Radiol 2003;14 : 1437-1442[Medline]
  7. Goldberg SN, Gazelle GS. Radiofrequency tissue ablation: physical principles and techniques for increasing coagulation necrosis. Hepatogastroenterology 2001;48 : 359-367[Medline]
  8. Hinshaw JL, Laeseke PF, Winter TC, Kliewer MA, Fine JP, Lee FT, Jr. Radiofrequency ablation of peripheral liver tumors: intraperitoneal 5% dextrose in water decreases postprocedural pain. AJR2006; 186:S306 -S310[Abstract/Free Full Text]
  9. Farrell MA, Charboneau JW, Callstron MR, Reading CC, Engen DE, Blute ML. Paranephric water instillation: a technique to prevent bowel injury during percutaneous renal radiofrequency ablation. AJR2003; 181:1315 -1317[Free Full Text]
  10. Srivastava DN, Gandhi D, Seith A, Pande GK, Dahni P. Transcatheter arterial embolization in the treatment of symptomatic cavernous hemangiomas of the liver: a prospective study. Abdom Imaging2001; 26:510 -514[CrossRef][Medline]
  11. Mitsuhashi N, Furuta M, Sakurai H, et al. Outcome of radiation therapy for patients with Kasabach-Merritt syndrome. Int J Radiat Oncol 1997; 39:467 -473[CrossRef][Medline]
  12. Cui Y, Zhou L, Dong M, et al. Ultrasonography guided percutaneous radiofrequency ablation for hepatic cavernous hemangioma. World J Gastroenterol 2003; 9:2132 -2134[Medline]
  13. Zagoria RJ, Roth TJ, Levine EA, Kavanagh PV. Radiofrequency ablation of a symptomatic hepatic cavernous hemangioma. AJR 2004; 182:210 -212[Free Full Text]

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