Abstract
Congenital vascular malformations (CVM) are a group of unique vascular disorders that can be defined as “diffuse or localized embryologically developed errors of vascular morphogenesis leading to true structural anomalies”. The presence of CVM in the general population is estimated to be around 1.5 %, with no known sex predilection. Venous malformations are the most common type of CVM, and they comprise approximately two-thirds of all CVMs. The diagnosis and treatment of CVM can be complex and challenging. Patients with CVM can easily be misdiagnosed and also mismanaged. Consequently, many patients have been discouraged by the lack of correct diagnosis and proper treatment despite numerous visits to different clinics (from primary care physicians to subspecialists). Moreover, patients with CVM have frequently been left untreated, due to the mistaken presumption that these types of lesions can spontaneously regress, while others were considered too high risk to treat. This chapter discusses CVM: classification, multidisciplinary approach diagnosis, and management.
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Keywords
- Vascular Malformation
- Venous Malformation
- Infantile Hemangioma
- Lymphatic Malformation
- Sodium Tetradecyl Sulfate
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
1 Introduction
Congenital vascular malformations (CVM) are a group of unique vascular disorders that can be defined as “diffuse or localized embryologically developed errors of vascular morphogenesis leading to true structural anomalies” [1]. The presence of CVM in the general population is estimated to be around 1.5 %, with no known sex predilection [2]. Venous malformations are the most common type of CVM, and they comprise approximately two-thirds of all CVM [3, 4]. The estimated incidence of predominantly venous malformations is approximately 0.8–1 % [5]. The majority of CVM arise sporadically, but in rare cases (1–2 %), they are familial and characterized by an autosomal dominant pattern of inheritance [6–8]. Although genetic mutations are suspected to be the underlying etiology, the exact mechanism responsible for development of CVM still remains to be elucidated [9–14].
The diagnosis and treatment of CVM can be complex and challenging since it exceeds the level of expertise of any single medical specialty. Patients with CVM can easily be misdiagnosed and also mismanaged. Consequently, many patients have been discouraged by the lack of correct diagnosis and proper treatment despite numerous visits to different clinics (from primary care physicians to subspecialists). Moreover, patients with CVM have frequently been left untreated, due to the mistaken presumption that these types of lesions can spontaneously regress, while others were considered too high risk to treat.
2 Classification
Historically, numerous attempts have been made to classify CVM [15–19]. Early classification published by Virchow divided all vascular lesions into angiomas and lymphangiomas [20]. This classification was based on the vessels’ histopathologic appearance and did not consider biological behavior and natural history of the lesion. Thus, there was a tendency to classify any type of vascular anomaly as a hemangioma. This tendency still persists among practitioners. Based on endothelial characteristics and on a biologic classification of vascular birthmarks, initially proposed by Mullikin and Glowicki in 1982, the International Society for the Study of Vascular Anomalies (ISSVA) approved in 1996 a classification system in which all vascular anomalies were divided on the basis of cellular kinetics, anatomy, and clinical behavior into two major categories: vascular tumors and vascular malformations [21, 22]. Depending on the type of vessel involved, vascular malformations were subdivided into high-flow vascular malformations (HFVM), such as arteriovenous malformation, and low-flow vascular malformations (LFVM), such as capillary, venous, and lymphatic malformations (Fig. 17.1). Based on their embryonic stage of developmental arrest, there are two different types of venous malformations: extratruncular and truncular as emphasized in the Modified Hamburg’s Classification [23]. Extratruncular venous malformations are the outcome of developmental arrest in the early stages, whereas truncular venous malformations are a result of developmental arrest in the late stages of embryogenesis. Extratruncular malformations are associated with a higher rate of recurrence and resistance to therapy, presumably because they possess mesenchymal characteristics of independent growth potential [24]. There are also complex-combined vascular malformations that are typically associated with osteomuscular hypertrophy and various internal organ anomalies.
The separation of vascular anomalies into tumors and malformations permits more effective communication between different medical specialists, since, as previously mentioned, the management of CVM has been characterized by confusing and contradictory nomenclature and classification that was present in the majority of the medical literature discussing these lesions. Unfortunately, despite the ISSVA classification, the use of confusing nomenclature persists in the literature, and archaic terms such as “cavernous hemangioma,” “port wine stains,” “salmon patch,” “angel’s kiss,” and “nevus simplex” are still frequently used by some specialists.
3 Pathophysiology
Congenital vascular malformations arise by vascular dysmorphogenesis, between the fourth and tenth weeks of intrauterine life, without increased endothelial proliferation affecting a limited number of vessels in a restricted area of the body [3]. Recent data suggest that the pathophysiologic mechanism underlying the formation of CVM is caused by dysfunctions in the signaling process responsible for regulation of proliferation, differentiation, maturation, adhesion, and apoptosis of vascular cells [25–27]. A genetic TIE2 mutation has been described in certain hereditary cutaneomucosal venous malformations [28]. A number of genes have also been identified in the process of lymphangiogenesis including VEGFR3, VEGFC, Ang2, Lyve1, Nrp2, and podoplanin [29]. It is postulated that genetic aberrations of these genes and their regulatory mechanisms underline developmental defects during embryonic lymphangiogenesis, resulting in lymphatic malformations. In contrast to CVM, vascular tumors are true neoplastic disorders, and pathohistologically they demonstrate increased endothelial cell turnover rate [26, 30]. Hemangiomas represent the most common type of vascular tumor. Less common vascular tumors include Kaposiform hemangioendothelioma, angiolipoma, angiosarcoma, and hemangiopericytoma. Although hemangiomas and CVM have distinct histopathologic characteristics and clinical courses, occasionally, they coexist in the same settings, suggesting a possible overlap in the pathogenesis of the vascular tumors and malformations in certain cases [31].
4 Clinical Presentation
The differential diagnosis of vascular tumors and vascular malformations can be made by clinical assessment in the majority of cases. Vascular malformations are present at birth and do not spontaneously regress. Often they grow proportionately with the child’s growth with many becoming more prominent later in life. Their rapid growth and appearance may be stimulated by trauma, infection, and the effects of hormones (during puberty or pregnancy), or they may occur spontaneously in the absence of any identified triggering factors [32]. By contrast, infantile hemangiomas are characterized by a rapid proliferative phase in the first several months of life, followed by an involutional phase of slow, spontaneous regression in the majority of cases, frequently leaving adipofibrotic overlying dermis and telangiectasias that can remain visible at the location of the initial hemangioma [33]. In challenging and complex cases, histopathologic evaluation, immunohistopathologic markers, and radiologic studies are needed to help distinguish vascular tumors from vascular malformations.
The morphology, clinical presentation, and course of vascular malformations are variable in their extent and severity, depending upon location, proximity to vital structures, size or organ involved, and the type of vessel affected. Congenital vascular malformations are rarely asymptomatic. Usually they cause discomfort, pain, hemorrhage, and negatively affect the patient’s appearance as well as emotional well-being. In addition, these patients often have a significant reduction in daily functional capacity and quality of life. As discussed previously, if the malformation has an arterial component, it is classified as HFVM. The absence of arterial blood flow is the characteristic used to differentiate HFVM from LFVM. Some authors use the term fast-flow or arteriovenous malformation to describe HFVM. Low-flow vascular malformations are subdivided into venous malformations, lymphatic malformations, capillary malformations, and lesions that combine two or more of these elements.
Capillary malformations usually appear as localized pink or red lesions. They are present at birth and grow in proportion to the growth of the child. They appear darker immediately after the birth and lighten slightly in the first several weeks of life. This is believed to be secondary to the higher hemoglobin concentration that characterize the immediate newborn period [34]. Capillary malformations can occur as isolated cutaneous lesions or in association with other vascular malformations or other structural abnormalities such as bony or soft tissue hyperplasia or atrophy and neurological defect. In the limbs, capillary malformations are usually associated with osteomuscular hypertrophy (Fig. 17.2). When located on the head, they may extend to the gingiva, lips, and oral mucosa. Midline occipital capillary malformations can herald the presence of an encephalocele or ectopic meninges. Capillary malformations over the spine can be associated with occult spinal dysraphism [35]. In a retrospective review, Guggisberg et al. suggested that the combination of two or more midline capillary malformations is highly suggestive of spinal dysraphism [36]. However, the significance of capillary malformations as a marker for underlying spinal abnormalities is still unclear, and currently there are no evidence-based guidelines regarding screening of patients with capillary malformations for spinal defects. The most common syndrome associated with capillary malformations is Sturge-Weber syndrome. This neuroectodermal syndrome is characterized by an overabundance of capillaries around the ophthalmic branch (V1) of the trigeminal nerve, ipsilateral leptomeningeal angiomatosis, glaucoma (in approximately 50 % of patients), and seizures. Seizures are frequently present within the first year of life and tend to worsen over time.
Venous malformations are the most common peripheral LFVM encountered clinically. They are composed of anomalous dilated venous channels. They affect males and females equally with a reported prevalence of approximately 1 % [37]. On physical examination they appear as bluish, soft, and easily compressible, non-pulsatile masses that usually enlarge with activity, Valsalva maneuver (crying in children) or dependent posture, and empty with elevation. There is no increase in local skin temperature or thrill when the malformation is palpated, and there is no bruit present on auscultation (in contrast to HFVMs) (Fig. 17.3). Venous malformations are associated with swelling and episodes of pain as well as functional difficulties secondary to the involvement of muscles and joints. Although most venous malformations are solitary and occur in the skin and subcutaneous tissues, they can also occur as multiple, infiltrating lesions that can involve multiple soft tissue planes including muscles, abdominal viscera, and the central nervous system [38]. In terms of connection to the conducting veins, venous malformations are characterized as sequestered or communicating. In contrast to sequestered venous malformations, communicating malformations have direct connection to deep venous system. It is important to determine whether malformation is communicating since treatment of this type of malformation carries an increased risk of distal venous thromboembolic events. Venous malformations can also occur as part of syndromes. Klippel-Trenaunay syndrome (KTS) is a complex capillary-lymphatic-venous malformation which is associated with pathognomonic osteomuscular hypertrophy of the affected extremities in association with mixed venous and lymphatic and capillary lesions [39, 40]. In addition to obvious concerns about cosmesis, these patients often present with pain, swelling, orthostatic hypotension, or in severe cases pulmonary embolism secondary to insufficiency of the anomalous vein structures or repeated occult pulmonary emboli from intralesional thrombus. Blue rubber bleb nevus syndrome (BRBNS) is another rare syndrome associated with venous malformations. This sporadic disorder is characterized by multifocal venous malformations of the skin, soft tissues, and gastrointestinal tract [41, 42]. In addition to the risk of bleeding and subsequent anemia, gastrointestinal involvement makes these patients susceptible to intussusception and volvulus [43].
Lymphatic malformations are usually noted at birth or before the patient reaches the age of 2 years. Prenatal ultrasonography (US) can detect macrocystic lymphatic malformations during the late first trimester. The skin overlying these sponge-like lesions is usually normal or of bluish hue (Fig. 17.4). Lymphatic malformations can be characterized as microcystic, macrocystic, or combined. Macrocystic lymphatic malformations are generally defined as lesions that contain cyst spaces greater than 2 cm and microcystic as cysts smaller than 2 cm in diameter. Bleeding, bacterial infection, and swelling are the most common complications associated with lymphatic malformations. These complications can lead to the compression of surrounding structures, including the airway (if the malformation is located in the head or neck), or the optic nerve in the case of orbital lesions. In these patients, prompt management and urgent decompression are required to decompress the lesion and subsequently restore the normal function of the affected vital structures. Infection is a common complication of lymphatic malformations, and prompt recognition and treatment with systemic antibiotics that cover skin pathogens is imperative.
5 Diagnosis
Despite distinct clinical, radiologic, and histological findings, LFVM are often confused with vascular tumors (most frequently with infantile hemangiomas) and many physicians do not understand the difference between these two vastly different lesions. Moreover, the complexity of many CVM contributes to the diagnostic challenge of differentiating LFVM from HFVM and differentiating LFVM from other congenital vascular anomalies. Since the prognosis, morbidity, and treatment significantly differ between vascular tumors, HFVM, and LFVM, proper diagnosis and accurate classification are critical for the successful management of these lesions [44]. A meticulous medical history and a detailed physical examination are essential initial steps in the management of CVM. However, clinical evaluation often underestimates the involvement of deep structures such as muscles, bones, joints, or abdominal viscera and is not sufficient to differentiate HFVM from LFVM and malformations from tumors in some of the more complicated lesions. Therefore, evaluation by advanced imaging modalities (color flow duplex ultrasound, magnetic resonance imaging) is of paramount importance for the correct diagnosis and management of CVM [45–47]. Ultrasonography of HFVMs is characterized by multidirectional blood flow and high-amplitude arterial waveform with spectral broadening. Ultrasonography of venous and lymphatic malformations reveals mixed venous waveform and complete absence of signal, respectively. On gray scale ultrasound, venous malformations appear as hypoechoic or heterogeneous lesions with anechoic structures visible in <50 % of cases. Duplex ultrasound of venous malformations generally demonstrates monophasic low-velocity flow. In some cases flow is only detectible with compression and release of the malformation. Macrocystic lymphatic malformations appear as anechoic cavities, often with internal septa and debris. Microcystic lymphatic malformations are hyperechoic, giving a more solid appearance.
In the evaluation of CVM, duplex ultrasound is useful to confirm the diagnosis, as it is rapid, readily available, and shows the flow velocity and vascularization [48]. It is also useful for initial assessment of superficial malformations; however it is frequently inadequate to demonstrate the extent of larger lesions. Therefore, magnetic resonance imaging (MRI) is the imaging modality of choice in the evaluation of CVM [49, 50]. It gives a bright hypersignal on T2-weighted spin-echo sequences that delineates the extent of the malformation throughout the involved tissues [51, 52]. In addition, MRI shows the lesion’s flow characteristics, relation to normal vascular and nonvascular structures, and provides good soft tissue definition (Fig. 17.5). In inconclusive cases, when suspicion of arterial flow is present based on MRI findings, an appropriate diagnostic workup includes an arteriogram, but only if treatment is deemed necessary. Every effort should be exerted to rule out a high-flow arterial component. It is worth emphasizing that this differentiation is of critical value in the management of CVM as treatment options for high-flow and low-flow lesions are different and the presence of an arterial component represents an absolute contraindication to transcutaneous sclerotherapy (due to the risk of arterial thrombosis and extensive tissue necrosis) which can be effectively used in the treatment of LFVM. In T2-weighted MRI, venous malformations demonstrate high-signal intensity, and this sequence is the best sequence to determine the full extent of the lesion and its relationship to adjacent tissues (Fig. 17.6a, b). Lymphatic malformations demonstrate predominantly fluid-type characteristics on all MRI sequences (low signal on T1 and high signal on T2 sequences). Macrocystic and microcystic components are easily differentiated since microcystic malformations demonstrate intermediate signal intensity on T1 and T2 spin-echo sequences.
From a diagnostic standpoint, evaluation of the deep venous system deserves special consideration. In a study of 392 patients with CVM, Eifert et al. documented aplasia or hypoplasia of deep venous trunks in 8 % of patients (with venous predominance) [2]. In these patients venous blood flow from the affected limbs depends on superficial and abnormal vessels. Obliteration of these venous structures would compromise the venous circulation of the affected limb. Evaluation of patency and anatomic variations of the entire venous system (deep and superficial) is vital in these patients (Fig. 17.7). It has been reported that the prevalence of deep venous anomalies is even higher (18 %) in patients with KTS [53]. Based on the venous drainage channels and their response to treatment and rates of complications, Puig et al. divided venous malformations into four types: isolated malformations without discernible venous drainage (type I), lesions draining into normal veins (type II), lesions draining into dysplastic veins (type III), and lesions consisting primarily of venous ectasia (type IV). According to the same authors, types I and II respond best to sclerotherapy and higher rates of complications are attributed to types III and IV [17].
In addition to being at increased risk of having deep venous anomalies, patients with extensive LFVMs may develop an intralesional consumptive coagulopathy [54, 55]. In a study of 118 patients, Mazoyer et al. demonstrated that localized intravascular coagulopathy (LIC) was present in 58 % of venous malformation patients [56]. In the literature, this coagulopathy is often erroneously labeled as Kasabach-Merritt syndrome (a distinct clinical entity characterized by disseminated intravascular coagulation and profound thrombocytopenia associated with vascular tumors) [57]. The platelet count in LIC is minimally diminished (in the 100–150 × 103/mL range). This distinction is important because, in contrast to patients with Kasabach-Merritt syndrome, LIC can be treated with heparin. Localized intravascular coagulopathy can be asymptomatic, but it may, rarely, be associated with painful intralesional thrombotic episodes and can progress to disseminated intravascular coagulation with life-threatening hemorrhage [58–60]. Although controversial, some authors advocate the use of aspirin or low molecular weight heparin (depending on the severity of symptoms) to be administered in patients with painful thrombotic episodes [58]. The increased risk of bleeding in some of these patients can be attributed to the increased consumption of coagulation factors. This is especially concerning in patients undergoing surgical resection of the lesion. A hypercoagulability profile should be considered in LFVM patients prior to undergoing imaging studies, surgical intervention, or sclerotherapy. An elevated D-dimer level and variable fibrinogen level is the hallmark of LIC. This finding is so common that some authors use D-dimer to differentiate venous malformations from lymphatic malformations (which do not show elevated D-dimer levels). Although LIC is usually latent and asymptomatic, it is worth emphasizing that these patients can become severely coagulopathic even during diagnostic procedures (US, MRI, angiography).
6 Treatment
Since the management of CVM falls in the range of several medical and surgical specialties, it is critical to establish a multidisciplinary approach for their diagnosis and treatment [61–64]. This was first discussed and introduced at the International Symposium for Congenital Vascular Malformations held in Seoul in 1996 [65]. In the past several years, several medical centers have developed multidisciplinary CVM teams [66]. Ideally, to achieve a consensus view of management, representatives from different medical specialties should be involved in the management of CVM patients and all treatments should be based on team assessments and decisions. This also affords the opportunity to streamline the evaluation process for patients with vascular anomalies, to coordinate the care of these patients, and to treat them comprehensively by reducing the need for multiple visits to different clinics. Given the heterogeneous nature and complexity of CVM, every patient and every lesion should be individually discussed. Multidisciplinary preoperative evaluation is of paramount importance, especially to rule out vascular tumors and to differentiate LFVM from HFVM and to identify lesions most amenable to resection. The decision for intervention has to take into account the size, location, proximity to vital structures and the natural history of the lesion, the risk of complications, and the relative risk of surgical or endovascular intervention. Low-flow vascular malformations can be treated with laser therapy, sclerotherapy, surgical excision, or combination therapy.
The flashlamp-pumped pulsed dye laser (FPDL) is the most frequently used as a treatment of choice for capillary malformations especially in areas in which there are concerns about ulcerations or hyperpigmentation from sclerotherapy. The most commonly used wavelengths are 577, 585, and 595 nm since they selectively target oxyhemoglobin. Pulse duration is used to concentrate and limit heat distribution (and subsequent collagen contraction and obliteration) to the capillary malformation while preserving surrounding structures in epidermis and dermis. Efficacy rates of the FPDL in the treatment of capillary malformations are variable. Reyes et al. reported good response in as many as 80 % of treated patients [67]. In a retrospective study of 259 adults and children, Renfro et al. demonstrated that responsiveness of the capillary malformations depends on the anatomical location of the lesion [68]. Lesions located on the central face or limbs were less responsive to FPDL than lesions located on the neck and trunk. It must be noted that multiple treatments are needed to achieve acceptable results. Treatments are usually scheduled every 6–8 weeks over the course of several months to a year depending upon the size, location, and responsiveness of the malformation to the therapy.
Despite the high rates of recurrence (25–52 %), surgical excision has been historically used as the treatment of choice for vascular malformations [69]. Traditionally, surgical resection was effectively used for encapsulated and small lesions. When a malformation is diffuse and multifocal, the surgical approach is relatively contraindicated as damage to major vital structures and massive hemorrhage may ensue. For larger lesions, complete surgical resection might not be possible and multiple partial surgical resections may be required. Partial surgical resections are associated with higher recurrence rates. Encapsulated, circumscribed, localized lesions and lesions composed of numerous small venous channels are the most amenable to surgical resection.
Since its introduction, sclerotherapy has been used as an effective alternative to surgery in the treatment of LFVM. Currently there are numerous agents available for sclerotherapy including ethanol, sodium tetradecyl sulfate (STS), polidocanol, ethibloc, and bleomycin. The most commonly used agents are ethanol and STS (in the United States) and polidocanol (in Europe), although the use of polidocanol in the United States has been increasing since its approval by the Food and Drug Administration (FDA) in March of 2010. Although proven to be effective [70, 71], ethanol sclerotherapy (ES) is associated with limitations and major side effects (local and systemic), including severe pain requiring general anesthesia, ethanol toxicity, and local tissue damage, and its use in pediatric patients remains controversial. In a study of 71 patients, Mason et al. demonstrated that patients who received up to 1 mL/kg of ethanol during ethanol embolization or sclerotherapy may have elevated serum ethanol levels that could be associated with increased risk of respiratory depression, cardiac arrhythmias, seizures, rhabdomyolysis, and hypoglycemia [72]. In a study of 98 sessions of ES in 30 CVM patients, Lee et al. documented complications in 26.7 % of patients which ranged from mild to severe and acute to delayed [73]. Authors reported nine cases with ischemic bullae, two with tissue fibrosis, two with tissue necrosis, one with deep venous thrombosis (DVT), one with pulmonary embolism, five with nerve palsy, and four cases of transient pulmonary pressure elevation. Of the five nerve palsies, one (affecting the peroneal nerve) was permanent. Other studies reported episodes of transient bradycardia and cardiac arrest during the treatment with ES [74]. Ethanol sclerotherapy can also result in transmural vessel necrosis, massive swelling (sometimes resulting in compartment syndrome), central nervous system (CNS) depression, hypertension, and pulmonary vasospasm [75, 76]. Some practitioners recommend continuous pulmonary pressure monitoring during ES and avoiding ethanol in regions adjacent to nerves such as the facial nerve or the sympathetic plexus in cervical lesions [76].
Since liquid sclerosants become diluted and inactivated by intralesional blood, the use of sclerosants in microfoam form significantly improves the procedure for LFVM [77–79]. The foam bubbles displace intralesional blood (preventing the sclerosant from becoming diluted) and achieve maximal effective exposure between the sclerosing agent and the endothelial lining. In addition, the echogenicity of the bubbles makes them visible on US surveillance making the procedure easier to perform (Figs. 17.8a, b). Foam treatments, in contrast to ES, can be given on a strictly ambulatory basis as they are minimally painful.
The use of foam sclerosants was initially described by Orbach in 1944 [80], and foam sclerotherapy gained popularity in the last decade. Foam can be produced with different techniques that result in differences in bubble size, foam stability, and reabsorption rates [81–83]. In 2000, Tessari reported a new method for microfoam production, using two syringes connected with a three-way stopcock (Fig. 17.9) [84]. Since then, this technique has been widely accepted in producing stable foam for the treatment of vein disorders. STS is a synthetic, detergent-based sclerosant, first described by Reiner in 1946 [85]. The mechanism of action is the creation of irreversible chemical damage to the vascular endothelial lining by the disruption of cell membranes. The response to the subendothelial collagen exposure is vasospasm, platelet aggregation, and subsequent endofibrosis that obliterates the vessel. Different concentrations of STS solution have been commonly used in the treatment of telangiectasias and reticular veins [86–89]. However, larger veins (greater than 10 mm in diameter) have also been effectively treated with STS [90]. In a double-blind prospective comparative trial that included 129 patients with varicose veins and telangiectasias, Goldman demonstrated that STS and polidocanol had approximately the same effectiveness and that there was no significant difference in adverse effects between these two sclerosants [91]. The properties of sclerosant in the form of microfoam made it possible to use smaller doses, decreasing the risk of side effects and toxicity. The echogenicity of microfoam bubbles made them visible on US surveillance, ensuring that the injection of STS was intraluminal and preventing extravasation necrosis.
Adverse events described with STS are skin hyperpigmentation and allergic reactions (ranging from urticaria to anaphylaxis). Patients susceptible to allergic reactions should be treated with precaution regarding prophylaxis. Skin hyperpigmentation depends on skin type, and its incidence parallels that of other sclerosing agents. Recently, some authors have voiced concern that foam-induced microembolism is a common phenomenon during foam sclerotherapy and that caution should be utilized in using foam sclerotherapy, especially in patients with a patent foramen ovale [92]. To minimize the possibility of distal embolic events, all malformations with arterial flow should be excluded prior to starting the treatment using the diagnostic methodologies discussed above.
Cabrera et al. published the first study of a large group of patients treated by foam sclerotherapy [93]. The report included 50 patients (35 with venous malformations and 15 with KTS). Sclerotherapy was performed by US-guided injection of 0.25–4 % polidocanol microfoam. The treatment was beneficial in 46 (92 %) patients. Eighteen showed total disappearance of treated malformation, 15 had a reduction in malformation size of more than 50 %, and 13 showed a reduction in malformation size of 50 % or less. Out of the 39 patients who presented with pain, 25 experienced total relief, and in the remaining 14 patients, the pain was significantly reduced. There were no major adverse events. Skin necrosis developed in three patients, and four patients developed transient skin hyperpigmentation. Another study that confirmed the efficacy of foam sclerotherapy was that of Bergan’s group [94]. Dr. Bergan reported a retrospective study on the efficiency and safety of outpatient treatment of LFVM based on 14 patients (eight with KTS) who were treated with polidocanol foam sclerotherapy. Foam was produced by the Tessari technique using 1 or 2 % polidocanol, specific for each patient. This study demonstrated that the use of polidocanol foam sclerotherapy was effective and was associated with no major complications, no recovery time, and no anesthetic requirements. The most recent data from a prospective study evaluating 135 patients with CVM (77.2 % were LFVM) treated at our institution demonstrate that symptoms in 93.5 % of patients significantly improved or resolved following US-guided foam sclerotherapy with STS or polidocanol. There were no complications. In a subgroup of LFVM patients treated with ES, symptoms significantly improved in 42.9 % of cases, and complication rate was 57.1 % (DVT, ulceration at the site of injection, bradycardia, and oxygen desaturation during the procedure). Consistent with these findings, we previously reported similar STS efficacy rates. 91.7 % of patients treated at our institution with STS had significant symptom improvement, and STS foam sclerotherapy was associated with no complications [95].
7 Conclusion
Vascular malformations are complex lesions that still pose a serious diagnostic and therapeutic challenge. During the last two decades, numerous efforts have been made to improve the management of patients with LFVM. Proper classification, MRI, US-guided sclerotherapy, and introduction of the multidisciplinary team concept all represent advancements in the management of this traditionally underserved population. However, further research is warranted to provide insights into the genetics and pathogenesis of vascular malformations. In addition, level 1 data from prospective, double-blind, controlled, randomized clinical trials are needed to compare therapeutic efficacy and safety of different sclerosing agents and surgical approach in the treatment of this challenging patient population.
References
Mulliken JB, Glowacki J. Hemangiomas and vascular malformations in infants and children. A classification based on endothelial characteristics. Plast Reconstr Surg. 1982;69:412–22.
Eifert S, Villavicencio JL, Kao TC, Taute BM, Rich NM. Prevalence of deep venous anomalies in congenital vascular malformations of venous predominance. J Vasc Surg. 2000;31:462–71.
Young AE. Pathogenesis of vascular malformations. In: Mulliken JB, Young AE, editors. Vascular birthmarks: hemangiomas and malformations. Philadelphia: W.B. Saunders Co; 1988. p. 107–13.
Villavicencio JL, Scultetus A, Lee BB. Congenital vascular malformations: when and how to treat them. Semin Vasc Surg. 2002;15(1):65–71.
Tasnadi G. Epidemiology and etiology of congenital vascular malformations. Semin Vasc Surg. 1993;6:200–3.
Boon LM, Mulliken JB, Enjolras O, Vikkula M. Glomuvenous malformation (glomangioma) and venous malformation: distinct clinicopathologic and genetic entities. Arch Dermatol. 2004;140(8):971–6.
Blei F, Walter J, Orlow SJ, Marchuk DA. Familial segregation of hemangiomas and vascular malformations as an autosomal dominant trait. Arch Dermatol. 1998;134:718–22.
Gallione CJ, et al. A gene for familial venous malformations maps to chromosome 9p in a second large kindred. J Med Genet. 1995;32(3):197–9.
Boon LM, Mulliken JB, Vikkula M, et al. Assignment of a locus for dominantly inherited venous malformations to chromosome 9p. Hum Mol Genet. 1994;3:1583–7.
Calvert JT, et al. Allelic and locus heterogeneity in inherited venous malformations. Hum Mol Genet. 1999;8(7):1279–89.
Irrthum A, Brouillard P, Boon LM, Warman ML, Olsen BR, Mulliken JB, Enjolras O, Vikkula M. Linkage disequilibrium narrows locus for venous malformations with glomus cells (VMGLOM) to a single 1.48-Mbp YAC. Eur J Hum Genet. 2001;9:34–8.
Cohen Jr MM. Vasculogenesis, angiogenesis, hemangiomas, and vascular malformations. Am J Med Genet. 2002;108(4):265–74.
Brouillard P, Olsen BR, Vikkula M. High-resolution physical and transcript map of the locus for venous malformations with glomus cells (VMGLOM) on chromosome 1p21-p22. Genomics. 2000;67(1):96–101.
Diehl S, et al. Altered expression patterns of EphrinB2 and EphB2 in human umbilical vessels and congenital venous malformations. Pediatr Res. 2005;57(4):537–44.
Degni M, Gerson L, Ishikava K, et al. Classification of the vascular diseases of the limbs. J Cardiovasc Surg. 1973;14:109–16.
Belov S. Anatomopathological classification of congenital vascular defects. Semin Vasc Surg. 1993;6:219–24.
Puig S, Aref H, Chigot V, Bonin B, Brunelle F. Classification of venous malformations in children and implications for sclerotherapy. Pediatr Radiol. 2003;33:99–103.
Marler JJ, Mulliken JB. Vascular anomalies: classification, diagnosis, and natural history. Facial Plast Surg Clin North Am. 2001;9(4):495–504.
Bartels C, Horsch S. Classification of congenital arterial and venous vascular malformations. Angiology. 1995;46(3):191–200.
Virchow R, editor. Die krankhaftenGeschwu¨ lste. Berlin: A. Hirschwald; 1863. p. 456–61.
Enjolras O, Mulliken JB. Vascular tumors and vascular malformations, new issues. Adv Dermatol. 1997;13:375–423.
Chiller KG, Frieden IJ, Arbiser JL. Molecular pathogenesis of vascular anomalies: classification into three categories based upon clinical and biochemical characteristics. Lymphat Res Biol. 2003;1(4):267–81.
Belov S. Classification of congenital vascular defects. Int Angiol. 1990;9(3):141–6.
Lee BB. Critical issues in management of congenital vascular malformation. Ann Vasc Surg. 2004;18(3):380–92.
Vikkula M, Boon LM, Mulliken JB, Olsen BR. Molecular basis of vascular anomalies. Trends Cardiovasc Med. 1998;8:281.
Lawley LP, Cerimele F, Weiss SW, North P, Cohen C, Kozakewich HPW, Mulliken JB, Arbiser JL. Expression of wilms tumor 1 gene distinguishes vascular malformations from proliferative endothelial lesions. Arch Dermatol. 2005;141:1297–300.
Morris PN, et al. Functional analysis of a mutant form of the receptor tyrosine kinase Tie2 causing venous malformations. J Mol Med. 2005;83(1):58–63.
Wouters V, Limaye N, Uebelhoer M, et al. Hereditary cutaneomucosal venous malformations are caused by TIE2 mutations with widely variable hyper-phosphorylating effects. Eur J Hum Genet. 2010;18:414–20.
Puig S, Casati B, Staudenherz A, Paya K. Vascular low-flow malformations in children: current concepts for classification, diagnosis and therapy. Eur J Radiol. 2005;53:35–45.
Mulliken JB, Fishman SJ, Burrows PE. Vascular anomalies. Curr Probl Surg. 2000;37:517.
Frieden IJ, Garzon M, Enjolras O. Vascular tumors and vascular malformations: does overlap occur? In: Program and abstracts of the 12th International Workshop on Vascular Anomalies, Berlin; June 27–28, 1998.
Enjolras O, Wassef M, Chapot R. A color atlas of vascular tumors and vascular malformations. New York: Cambridge University Press; 2007.
Boon LM, Enjolras O, Mulliken JB. Congenital hemangioma: evidence of accelerated involution. J Pediatr. 1996;128:329–35.
Cordoro KM, Speetzen LS, Koerper MA, et al. Physiologic changes in vascular birthmarks during early infancy: mechanisms and clinical implications. J Am Acad Dermatol. 2009;60(4):669–75.
Boyvat A, et al. Lumbosacral vascular malformation: a hallmark for occult spinal dysraphism. Dermatology. 2000;201(4):374–6.
Guggisberg D, Hadj-Rabia S, Vinet C, et al. Skin markers of occult spinal dysraphism in children: a review of 54 cases. Arch Dermatol. 2004;140(9):1109–15.
Legiehn GM, Heran MK. Venous malformations: classification, development, diagnosis, and interventional radiologic management. Radiol Clin North Am. 2008;46:545–97.
Hein KD, et al. Venous malformations of skeletal muscle. Plast Reconstr Surg. 2002;110(7):1625–35.
Gloviczki P, et al. Klippel-Trenaunay syndrome: the risks and benefits of vascular interventions. Surgery. 1991;110(3):469–79.
Lee A, et al. Evaluation and management of pain in patients with Klippel-Trenaunay syndrome: a review. Pediatrics. 2005;115(3):744–9.
Nahm WK, et al. Venous malformations in blue rubber bleb nevus syndrome: variable onset of presentation. J Am Acad Dermatol. 2004;50(5 Suppl):S101–6.
Andersen JM. Blue rubber bleb nevus syndrome. Curr Treat Options Gastroenterol. 2001;4(5):433–40.
Rossler L, Lamesch A. The blue rubber bleb nevus or the cellular blue nevus or Bean syndrome. A rare case of iron-deficiency anemia. Phlebologie. 1992;45(4):471–5.
Lee BB, et al. Congenital vascular malformations: general diagnostic principles. Phlebology. 2007;22(6):253–7.
Dubois J, Garel L, Grignon A, et al. Imaging of hemangiomas and vascular malformations in children. Acad Radiol. 1998;5(5):390–400.
Paltiel HJ, Burrows PE, Kozakewich HP, Zurakowski D, Mulliken JB. Soft-tissue vascular anomalies: utility of US for diagnosis. Radiology. 2000;214(3):747–54.
Dubois J, et al. Soft-tissue venous malformations in adult patients: imaging and therapeutic issues. Radiographics. 2001;21(6):1519–31.
Trop I, et al. Soft-tissue venous malformations in pediatric and young adult patients: diagnosis with Doppler US. Radiology. 1999;212(3):841–5.
Burrows PE, Laor T, Paltiel H, Robertson RL. Diagnostic imaging in the evaluation of vascular birthmarks. Dermatol Clin. 1998;16(3):455–88.
Wilms G, et al. MRI of non-ischemic vascular disease: aneurysms and vascular malformations. Eur Radiol. 1999;9(6):1055–60.
Herborn CU, et al. Comprehensive time-resolved MRI of peripheral vascular malformations. AJR Am J Roentgenol. 2003;181(3):729–35.
Dubois J, Garel L. Imaging and therapeutic approach of hemangiomas and vascular malformations in the pediatric age group. Pediatr Radiol. 1999;29(12):879–93.
Browse NL, Burnand KG, Lea TM. The Klippel-Trenaunay syndrome. In: Browse NL, Burnand KG, Thomas ML, editors. Diseases of the veins: pathology, diagnosis and treatment. London: Edward Arnold; 1988. p. 609–25.
Enjolras O, Ciabrini D, Mazoyer E, Laurian C, Herbreteau D. Extensive pure venous malformations in the upper or lower limb: a review of 27 cases. J Am Acad Dermatol. 1997;36(2, pt 1):219–25.
Mazoyer E, Enjolras O, Laurian C, Houdart E, Drouet L. Coagulation abnormalities associated with extensive venous malformations of the limbs: differentiation from Kasabach-Merritt syndrome. Clin Lab Haematol. 2002;24(4):243–51.
Mazoyer E, et al. Coagulation disorders in patients with venous malformation of the limbs and trunk: a case series of 118 patients. Arch Dermatol. 2008;144(7):861–7.
Enjolras O, Mulliken JB, Wassef M, et al. Residual lesions after Kasabach-Merritt phenomenon in 41 patients. J Am Acad Dermatol. 2000;42(2, pt 1):225–35.
Dompmartin A, et al. Association of localized intravascular coagulopathy with venous malformations. Arch Dermatol. 2008;144(7):873–7.
Hermans C, et al. Venous malformations and coagulopathy. Ann Chir Plast Esthet. 2006;51(4–5):388–93.
Mazereeuw-Hautier J, et al. Extensive venous/lymphatic malformations causing life-threatening haematological complications. Br J Dermatol. 2007;157(3):558–63.
Lee BB, Bergan JJ. Advanced management of congenital vascular malformations: a multidisciplinary approach. Cardiovasc Surg. 2002;10(6):523–33.
Donnelly LF, Adams DM, Bisset 3rd GS. Vascular malformations and hemangiomas: a practical approach in a multidisciplinary clinic. AJR Am J Roentgenol. 2000;174(3):597–608.
Nagy M, Brodsky L. Multidisciplinary approach to management of hemangiomas and vascular malformations. Facial Plast Surg Clin North Am. 2001;9(4):551–9.
Redondo P. The hidden face of venous malformations: a multidisciplinary therapeutic approach. Arch Dermatol. 2008;144(7):922–6.
Lee BB. What is new in venous disease: new approach to old problem of venous disease: congenital vascular malformation. In: Angelides NS, editor. Advances in phlebology. Limassol: Hadjigeogiou Printing & Co; 1998. p. 59–64.
Erin FDM, et al. Clinical characteristics and management of vascular anomalies: findings of a multidisciplinary vascular anomalies clinic. Arch Dermatol. 2004;140(8):979–83.
Reyes BA, Geronemus R. Treatment of port-wine stains during childhood with the flashlamp-pumped pulsed dye laser. J Am Acad Dermatol. 1990;23(6 Pt 1):1142–8.
Renfro L, Geronemus RG. Anatomical differences of port-wine stains in response to treatment with the pulsed dye laser. Arch Dermatol. 1993;129(2):182–8.
Mathur NN, Rana I, Bothra R, Dhawan R, Kathuria G, Pradhan T. Bleomycin sclerotherapy in congenital lymphatic and vascular malformations of head and neck. Int J Pediatr Otorhinolaryngol. 2005;69:75–80.
Svendsen P, Wikholm G, Fogdestam I, Naredi S, Edén E. Instillation of alcohol into venous malformations of the head and neck. Scand J Reconstr Hand Surg. 1994;28:279–84.
Yakes WF, Luethke JM, Parker SH, Stavros AT, Rak KM, Hopper KD, et al. Ethanol embolization of vascular malformations. Radiographics. 1990;10:787–96.
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;217:127–32.
Lee BB, Kim DI, et al. New experiences with absolute ethanol sclerotherapy in the management of a complex form of congenital venous malformation. J Vasc Surg. 2001;33(4):764–72.
Yakes WF, Baker R. Cardiopulmonary collapse: sequelae of alcohol embolotherapy. Radiology. 1993;189:145.
Yakes WF, et al. Symptomatic vascular malformations: ethanol embolotherapy. Radiology. 1989;170(3 Pt 2):1059–66.
Burrows PE, Mason KP. Percutaneous treatment of low flow vascular malformations. J Vasc Interv Radiol. 2004;15(5):431–45.
Yamaki T, et al. Prospective randomized efficacy of ultrasound-guided foam sclerotherapy compared with ultrasound-guided liquid sclerotherapy in the treatment of symptomatic venous malformations. J Vasc Surg. 2008;47(3):578–84.
Bergan J, Cheng V. Foam sclerotherapy of venous malformations. Phlebology. 2007;22(6):299–302.
Yamaki T, Nozaki M, Iwasaka S. Comparative study of duplex-guided foam sclerotherapy and duplex-guided liquid sclerotherapy for the treatment of superficial venous insufficiency. Dermatol Surg. 2004;30(5):718–22. discussion 722.
Orbach EJ. Sclerotherapy of varicose veins—utilization of an intravenous air block. Am J Surg. 1944;66:362–6.
Eckmann DM, Kobayashi S, Li M. Microvascular embolization following polidocanol microfoam sclerosant administration. Dermatol Surg. 2005;31:636–43.
Frullini A. New technique in producing sclerosing foam in a disposable syringe. Dermatol Surg. 2000;26:705–6.
Rao J, Goldman MP. Stability of foam in sclerotherapy: differences between sodium tetradecyl sulfate and polidocanol and the type of connector used in the double-syringe system technique. Dermatol Surg. 2005;31(1):19–22.
Tessari L, Cavezzi A, Frullini A. Preliminary experience with a new sclerosing foam in the treatment of varicose veins. Dermatol Surg. 2001;27:58–60.
Reiner L. The activity of anionic surface active compounds in producing vascular obliteration. Proc Soc Exp Biol Med. 1946;62:49.
Lucchi M, Bilancini S, Tucci S. Sclerosis with foam of the great saphenous vein—short term results. Phlebologie. 2003;4:389–94.
Rao J, Wildemore JK, Goldman MP. Double-blind prospective comparative trial between foamed and liquid polidocanol and sodium tetradecyl sulfate in the treatment of varicose and telangiectatic leg veins. Dermatol Surg. 2005;31(6):631–5. discussion 635.
Stirling M, Shortell CK. Endovascular treatment of varicose veins. Semin Vasc Surg. 2006;19(2):109–15.
Bergan J, Cheng V. Foam sclerotherapy for the treatment of varicose veins. Vascular. 2007;15(5):269–72.
Barrett J, Allen B, Ockelford A, Goldman MP. Microfoam ultrasound- guided sclerotherapy for varicose veins in a subgroup with diameter at the junction of > 10 mm compared with a subgroup < 10 mm. Dermatol Surg. 2004;30:1386–90.
Goldman MP. Treatment of varicose and telangiectatic leg veins. Double-blind prospective comparative trial between aethoxyskerol and sotradecol. Dermatol Surg. 2002;28:52–5.
Ceulen RP, Sommer A, Vernooy K. Microembolism during foam sclerotherapy of varicose veins. N Engl J Med. 2008;358(14):1525–6.
Cabrera J, Cabrera J, Garcia-Olmedo MA, Redondo P. Treatment of venous malformations with sclerosant in microfoam form. Arch Dermatol. 2003;139:1494–6.
Pascarella L, Bergan JJ, Yamada C, Mekenas L. Venous angiomata: treatment with sclerosant foam. Ann Vasc Surg. 2005;19:457–64.
Markovic JN, Shortell CK. Initial experience in the treatment of low flow vascular malformations with sodium tetradecyl sulfate foam sclerotherapy. Presented at the 62nd Vascular Annual Meeting of the Society for Vascular Surgery. San Diego; June 2008.
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Markovic, J.N., Shortell, C.K. (2014). Low-Flow Vascular Malformations. In: Mowatt-Larssen, E., Desai, S., Dua, A., Shortell, C. (eds) Phlebology, Vein Surgery and Ultrasonography. Springer, Cham. https://doi.org/10.1007/978-3-319-01812-6_17
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