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AJR 2003; 180:1399-1401
© American Roentgen Ray Society


Technical Innovation

Double-Needle Sclerotherapy of Lymphangiomas and Venous Angiomas in Children: A Simple Technique to Prevent Complications

Stefan Puig1,2, Hussein Aref1,3 and Francis Brunelle1

1 Department of Pediatric Radiology, Necker Hôpital Enfants Malades, 149 Rue Sevres, Paris 75015, France.
2 Present address: Department of Radiology, University of Vienna, Waehringer Guertel 18-20, 1090 Vienna, Austria.
3 Present address: Department of Radiology, University of Alexandria, 1 Khartoum Sq., Alexandria, Egypt.

Received December 14, 2001; accepted after revision October 17, 2002.

 
Address correspondence to S. Puig.


Introduction
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Introduction
Materials and Methods
Results
Discussion
References
 
Percutaneous sclerotherapy involves the injection of a sclerosing substance intravascularly for the purpose of eradicating an abnormal blood vessel. Percutaneous sclerotherapy is a well-established method for the initial treatment of low-flow vascular malformations such as venous or lymphatic malformations. The percutaneous injection of pure ethanol is the preferred approach by many and has a high success rate [1]. The technique includes the direct puncture of the lesion under clinical or imaging localization. To achieve a satisfactory result, prolonged contact of the sclerosant with the endothelial lining of the lesion is required. However, prolonged contact is associated with a risk of extravasation of the sclerosant, which would result in an embolization of other than the targeted volume and potential neuropathy, tissue necrosis, or peripheral nerve palsy [1, 2, 3, 4, 5, 6]. If the alcohol enters the systemic vascular system, complications such as hypotension and various degrees of intoxication or even death may occur [3, 4, 5]. However, precisely because of its extremely powerful sclerosing properties, ethanol has proven to be efficacious in the treatment of vascular malformations. To reduce the risk of ethanol reflux into the superficial veins or the central venous system, we developed a technique whereby ethanol is drained via a second needle. The purpose of this article is to describe this new double-needle technique.


Materials and Methods
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Introduction
Materials and Methods
Results
Discussion
References
 
Since 1998, we have used the double-needle technique in 15 children with small, medium, and large vascular malformations. The malformations were located on the head or neck in seven patients (47%), on the trunk in two (13%), at the upper extremity in one (7%), and at the lower extremity in five (33%). All procedures were performed with the patient under general anesthesia. Because of the broad range of lesion sizes, a therapeutic outcome was considered satisfactory when a notable reduction in the volume of the vascular malformation was achieved.

After localization, a 22-gauge catheter is inserted into the lesion under fluoroscopic control. Phlebography, using a nonionic contrast medium, visualizes the true extent of the malformation and its hemodynamic characteristics. A second needle of the same size is then inserted into the lesion at some distance from the first needle to allow a rinsing flow of the liquid (Figs. 1A, 1B and 2). An initial check should guarantee that the contrast material is actually flowing out through the second needle. If the drainage is not sufficient, the second needle should be repositioned at another site under fluoroscopic control. A sclerosing agent is then injected. The overall injected volume depends on the size of the lesion but does not exceed the recommended dose of 1 mL/kg of body weight [2, 5]. Using digital subtraction angiography, we observed a direct visual correlation. During injection, liquid flows out through the second needle; when the injection is stopped, the outflow of liquid also ceases (Figs. 1A, 1B). The lesion filled with contrast material is used as a mask for digital subtraction angiography. Because of the injection of the sclerosing agent, the pressure in the lesion increases, and the liquid in the lesion flows along the path of least resistance. The liquid, which is a mixture of blood, ethanol, and contrast material, becomes visible under fluoroscopy when it enters the second needle but is also seen when it drains into the adjacent venous system. Thus, it is quite easy to control the flow of the sclerosing agent and, if reflux into the central venous system occurs, the procedure can be stopped immediately.



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Fig. 1A. Treatment of venous malformation in 7-year-old boy. Phlebogram shows malformation and venous drainage (arrows).

 


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Fig. 1B. Treatment of venous malformation in 7-year-old boy. Digital subtraction angiogram shows contrast material being administered via 22-gauge catheter (arrow). Note second needle (arrowhead) inserted into lesion. During injection of ethanol, residual contrast material flows out through second catheter. After ethanol has penetrated lesion, fluid exits venous malformation through second needle. No contrast material or ethanol enters normal adjacent veins.

 


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Fig. 2. Photograph shows double-needle technique for treating vascular malformation of neck. Contrast medium and sclerosing agent flow out through second needle (arrow).

 

When the lesion is located on a limb, a tourniquet can be used to exclude the vascular malformation from the rest of the venous system to provide additional safety. After the interventional procedure, all patients are hospitalized for observation for 24 hr and then are discharged if no complications occur. Analgesic therapy is administered for 8 days. Clinical follow-up took place 2 months after the procedure for patients living locally. Patients from abroad were followed up with correspondence.


Results
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Introduction
Materials and Methods
Results
Discussion
References
 
At our institution, 15 vascular malformations in two infants and 13 boys and girls (nine male, six female; age range, 7 months-17 years; mean age, 6.1 years) were treated using the double-needle technique. In each case, the greatest recommended dose of ethanol was injected within the limit of 1 mL/kg of body weight. The desired treatment result (i.e., partial or total reduction of the volume of the vascular malformation) was achieved in all 15 patients. No evident extravasation of alcohol occurred, nor were minor or major complications observed in any patient. In no case was a repetition of sclerotherapy or other treatment required. All patients were discharged after 24 hr of observation.


Discussion
Top
Introduction
Materials and Methods
Results
Discussion
References
 
As a treatment agent for percutaneous sclerotherapy, ethanol combines the benefits of wide availability, low cost, and powerful sclerosing properties [3]. Complications of ethanol injection include local tissue damage and potentially disastrous systemic effects. Local skin and nerve injuries are avoided by ensuring that the sclerosant remains intravascular and does not extravasate. Systemic complications are minimized by limiting the total dose of injected ethanol to 1 mL/kg of body weight. With the double-needle technique, the flow of ethanol is controlled locally by fluoroscopic visualization of the mixture with contrast material and systemically by ethanol leaving the lesion through the second needle.

The volume and pressure of blood in the vascular malformation and the adjacent venous system are important variables. Pressure in veins under static conditions is roughly equal to the pressure of blood reaching from the point of measurement to the level of the heart. For example, the mean pressure in the popliteal vein in young healthy persons in the horizontal position measures about 12 mm Hg [7]. When a vein or venous malformation is elevated above the level of the heart, the intravascular pressure and volume may approach zero [8]. The pressure of injection exerted through the syringe can easily exceed the pressure in the veins adjacent to and connected to the malformation. If that happens, sclerosing material will flow into the adjacent vessels. When the double-needle technique is used, the pressure in the second needle corresponds to the atmospheric air pressure, which is lower than the pressure in the adjacent and communicating venous system, provided the malformation is below the level of the heart. Patients in whom the lesion is located above the level of the heart should be properly positioned before the intervention is begun.

During injection, the presence of the second needle allows the outflow of contrast material or alcohol without significant elevation of the pressure in the lesion (Figs. 1A, 1B and 2). The injected liquid will follow the path of least resistance. Therefore, ethanol should exit the lesion via the second needle without entering in the adjacent vessels. It is important to verify that there is free return from the second needle during the injection into the first. In patients in whom flow is not optimal, the needle should be repositioned or replaced. Although lymphatic malformations may sometimes be drained and injected through a single needle, these lesions are similarly treated using the double-needle technique because many of them are mixed lesions and others may not be known to be lymphatic alone before the injection.

It is difficult to evaluate our results using this technique in a small sample of pediatric patients. The vascular malformations varied in size and anatomic location, and no known parameters are used to assess therapeutic efficacy. However, in all patients, the goal of reduction of lesion size was achieved without complications.

In conclusion, our double-needle technique showed promising results. Larger studies are necessary to determine the advantages of this technique over other sclerotherapeutic methods.


References
Top
Introduction
Materials and Methods
Results
Discussion
References
 

  1. O'Donovan JC, Donaldson JS, Morello FP, Pensler JM, Vogelzang RL, Bauer B. Symptomatic hemangiomas and venous malformations in infants, children, and young adults: treatment with percutaneous injection of sodium tetradecyl sulfate. AJR 1997;169:723 –729[Abstract/Free Full Text]
  2. Mason KP, Michna E, Zurakowski D, Koka BV, Burrows PE. Serum ethanol levels in children and adults after ethanol embolization or sclerotherapy for vascular anomalies. Radiology 2000;217:127 –132[Abstract/Free Full Text]
  3. Gelczer RK, Charboneau JW, Hussain S, Brown DL. Complications of percutaneous ethanol ablation. J Ultrasound Med 1998;17:531 –533[Abstract]
  4. Garel L, Mareschal JL, Gagnadoux MF, Pariente D, Guilbert M, Sauvegrain J. Fatal outcome after ethanol renal ablation in child with end-stage kidneys. AJR 1986;146:593 –594[Free Full Text]
  5. Berenguer B, Burrows PE, Zurakowski D, Mulliken JB. Sclerotherapy of craniofacial venous malformations: complications and results. Plast Reconstr Surg 1999;104:1 –11[Medline]
  6. De Lorimier AA. Sclerotherapy for venous malformations. J Pediatr Surg 1996;30:188 –194
  7. Arnoldi CC. The influence of posture upon the pressure in the veins of the normal human leg at rest and during rhythmic muscular exercise. Acta Chir Scand 1966;131:423 –431
  8. Green D. Mechanism of action of sclerotherapy. Semin Dermatol 1993;12:88 –97[Medline]

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Arch Facial Plast SurgHome page
J. P. Deveikis
Percutaneous Ethanol Sclerotherapy for Vascular Malformations in the Head and Neck
Arch Facial Plast Surg, September 1, 2005; 7(5): 322 - 325.
[Abstract] [Full Text] [PDF]


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