Supermicrosurgical lymphaticovenular anastomosis vs. vascularized lymph vessel transplant - technical optimization and when to perform which
Abstract
Early surgical intervention for lymphedema can delay, prevent, and even reverse lymphatic degeneration. Vascularized lymph vessel transplant (VLVT) has emerged as an alternative to vascularized lymph node transplant (VLNT) for the treatment of advanced, fluid-predominant lymphedema, providing highly favorable outcomes with reduced donor-site complications. Lymphaticovenular anastomosis (LVA) has traditionally been reserved for early disease. However, technical refinements have improved its results and expanded its efficacy, creating an overlap between the indications for VLVT/VLNT and LVA. This article describes our technical approach to VLVT and LVA and explores the nuances of treatment selection in the light of their shifting indications.
Keywords
INTRODUCTION
Supermicrosurgical advancements over the past few decades have given rise to a myriad of efficacious options for surgical treatment of lymphedema. In contrast to traditional belief, recent evidence shows that early surgical intervention for lymphedema can delay, prevent, and even reverse lymphatic degeneration[1,2]. Supermicrosurgical lymphaticovenular anastomosis (LVA) and vascularized lymph node transplant (VLNT) are established physiologic techniques for the treatment of fluid-predominant lymphedema[3,4]. While VLNT is efficacious in the treatment of advanced, fluid-predominant lymphedema, its risk of iatrogenic donor-site lymphedema makes the procedure undesirable to many. Vascularized lymph vessel transplant (VLVT) has recently been introduced as a less-invasive alternative to VLNT for these advanced cases[5-7]. LVA is traditionally reserved for early-stage, fluid-predominant lymphedema. However, recent technical refinements have shown that the efficacy of LVA in advanced disease has been underestimated. With this expanded potential, there is now an overlap between the indications for LVA and VLVT/VLNT. This paper aims to share the technical and decision-making pearls for improving outcomes of LVA and VLVT, both of which are safe and powerful procedures to treat fluid-predominant lymphedema.
History of LVA and VLNT
Supermicrosurgical lymphaticovenular anastomosis and its precursor, microsurgical lymphovenous bypass (LVB), re-route native lymphatic vessels into the venous circulation of the affected extremity[8]. LVB was first described by Jacobson and Suarez[9] in a canine model in 1962. Simultaneously, Chang et al.[10] adapted this canine model to study lymphovenous bypass, lymph node-to-vein anastomosis, lymphatic vessel interposition grafts, and vein interposition grafts to bridge lymphatic defects. Techniques were refined by various others using canine and rat models[11-14]. In 1977, O’Brien et al.[15] published their series of microsurgical LVB in human proximal upper limbs. Because microsurgical techniques were still in development, the anastomoses were created in the proximal limb, which contains larger veins but more functionally impaired lymphatics. The combination of these high-pressure veins with lower-quality lymphatics resulted in inconsistent surgical outcomes[16-18]. Subsequent advances in pre- and intra-operative imaging, operating microscopes, and surgical instruments facilitated the anastomosis of vessels smaller than 0.8 mm in diameter, ushering in the era of supermicrosurgery[2]. First described by Koshima et al.[19] in 2000, supermicrosurgical LVA allowed for the anastomosis of smaller lymphatics with venules ranging from 0.1-0.6 mm in diameter. The ability to use smaller vessels allowed surgeons to operate in the distal extremity, where lymph vessel function was more likely to be intact and to select small, low-pressure venules that offered more favorable pressure gradients[19,20].
In 1979, Shesol performed a pedicled flap transfer of groin lymphatic tissues for popliteal fossa defects in rats, showing lymph flow reestablishment at 7 days[21]. It set the groundwork for the development of VLNT[22,23]. The mechanism of action of VLNT is believed to be due to: (1) bridging lymphangiogenesis mediated by lymphatic growth factors, particularly vascular endothelial growth factor C[24] secretion from the transplanted lymphatic tissue; and (2) “pumping” action-driven by perfusion gradients between arterial inflow and venous outflow[22-29]. However, there is no clear evidence that these mechanisms rely on the lymph nodes contained in these flaps. It has not been consistently demonstrated that different VLNT flap donor sites - which often contain different numbers of nodes - produce different outcomes[30-32]. The sole study comparing different VLNT flaps within a single institution did not demonstrate a significant difference[33], and studies attempting to establish a correlation between the number of LNs and the effectiveness of the flap have yielded mixed results[34,35]. Moreover, while it is difficult to compare VLNT flaps with and without skin paddles in a controlled manner, increasing understanding of the dermal and subcutaneous lymphatic system strongly suggests that lymphadiposal tissue is essential for the efficacy of the flap[36,37]. Additionally, lymphatic vessels are likely the main drivers of lymph pumping, as evidenced by their smooth muscle lining and peristaltic action. Now that advancements in lymphography allow precise pre- and intra-operative visualization of superficial lymph vessels, their pumping action can be harnessed with intentional inclusion in flaps and proper orientation in recipient sites[38]. Combined with lymphatic channels’ abilities to absorb lymph and stimulate lymphangiogenesis, it supports the hypothesis that vessels - not nodes - are the therapeutic components of these flaps[39,40].
Vascularized lymph vessel transplant - the third surgical alternative
Vascularized lymph vessel transplant was introduced by Koshima et al.[5] in 2016 when they used first dorsal metatarsal artery (FDMA)-based lymphadiposal flaps on treating advanced lymphedema in thirteen patients. It represented a conceptual departure from the accepted belief that nodal tissue transfer is required to restore of lymphatic drainage. Subsequently, the senior author implemented FDMA-based VLVT with favorable recipient-site outcomes. However, the location of the donor site precluded the flap’s use in bilateral lower extremity disease. Additionally, FDMA flap harvest frequently caused devascularization of the skin over the first metatarsal space, resulting in donor wound breakdown[7]. Nevertheless, the success of the procedure drove the senior author to establish alternative lymphatic-rich donor sites: the groin [superficial circumflex iliac artery perforator (SCIP) flap] and trunk [thoracodorsal artery perforator (TDAP) flap][6]. The SCIP flap’s familiar vascular anatomy and successful use as a thin flap make it an ideal candidate for VLVT. However, the SCIP flap is not a feasible option in patients with bilateral lower extremity lymphedema. The TDAP flap’s location makes it suitable for bilateral lower extremity disease and contralateral upper extremity disease. Our early outcomes show similar efficacy and safety profiles to that of the SCIP flap. As shown in Figure 1, satisfactory decompression of the lymphedematous limb with minimal complications is achievable. By selectively harvesting only lymph vessels and completely preserving lymph nodes, VLVT greatly reduces the risk of donor-site complications while still offering results comparable to VLNT. As of the writing of this article, the senior author (Chen WF) has completely replaced VLNT with VLVT in his practice for the treatment of advanced fluid-predominant lymphedema.
Figure 1. A representative case of TDAP-based VLVT for unilateral upper extremity lymphedema. (A) TDAP flap was harvested superficially to the superficial fascia for inset into the distal volar forearm. (B) Preoperative image showing significant swelling of the right upper extremity. (C) Measurements 3 months postoperatively show a significant reduction in the girth of the right upper extremity. The thin profile of VLVT flaps minimizes flap bulk; thus, contour deformity of the recipient site is avoided. TDAP: Thoracodorsal artery perforator; VLVT: vascularized lymph vessel transplant.
Revisiting the indications for LVA
As surgeons’ worldwide developed expertise in supermicrosurgery, the practice of LVA grew in sophistication. New technology and techniques further enhanced an already efficacious procedure. Indocyanine green (ICG)-lymphographic[41], infrared[42], and high-frequency duplex ultrasound[43,44] guidance facilitates the precise placement of small incisions with high success rates. Different anastomotic configurations were developed to increase the number of drainage pathways and to successfully complete LVA even under technically challenging conditions[45,46]. These technical innovations allowed supermicrosurgeons to successfully treat even advanced lymphedema cases with LVA when these cases were previously considered only treatable with VLNT. Because VLVT and VLNT have similar indications, with the expanding scope of LVA, indications for LVA and VLVT/VLVT have started to overlap.
Technical tips: LVA
Vessel mapping and dissection
Incisions for LVA are planned where ICG-mapped lymph vessels and infrared-mapped veins lie in close proximity, as shown in Figure 2, maximizing the possible number of LVAs created per incision[47-51]. The anatomy of the superficial lymphatic system closely follows that of the superficial venous system; thus, in advanced cases with difficult-to-identify lymphatics, careful dissection along main superficial veins can still reveal suitable lymph vessels[52], as shown in Figure 3. In these advanced cases, any dermal backflow pattern on delayed images of diagnostic ICG lymphography suggests the presence of lymphostatic choke points. LVAs incisions should ideally be placed anatomically in or just proximal to these dermal backflow patterns. Injection of isosulfan blue 2 cm distal to skin markings just before each incision enhances identification of lymphatic vessels during dissection[52]. We use 20-25x magnification and proceed in a caudo-cephalad direction[48]. All dissected lymphatics are inspected and graded as healthy, ectatic (mild injury), contracted (moderate injury), or sclerotic (severe injury)[16,53]. Although healthy vessels are preferred, ectatic and contracted vessels can also be used when necessary to achieve a sufficient number of LVAs per case[47,54].
Figure 2. Incision planning for LVA. (A) Lymphatic channels (solid green lines) are mapped with ICG lymphography, and veins are mapped (dotted blue lines) with an infrared vein finder. 2-3 cm incisions are marked in sites where veins and lymphatics lie in proximity (red lines). Green circles mark the sites used for ICG injection in a distal-to-proximal sequence. (B) Immediate postoperative picture depicting the location of selected venules and lymphatics at each incision, with diagrams of the anastomotic configurations chosen. Blue staining of skin seen at sites of isosulphan blue injection is used for enhanced visualization of lymphatic channels during dissection. LVA: Lymphaticovenular anastomosis; ICG: indocyanine green.
Figure 3. In this representative case of upper extremity lymphedema, ICG lymphography was contraindicated due to iodine allergy, necessitating intraoperative exploration to locate suitable lymphatics for LVA. (A) Because the anatomy of the superficial lymphatic system closely follows that of the superficial venous system, incisions (red lines) were planned near infrared-mapped veins (dotted blue lines). (B) All incisions used were positive for suitable lymphatic vessels; diagrams depict the anastomotic configurations chosen at each incision site. ICG: Indocyanine green; LVA: lymphaticovenular anastomosis.
Anastomosis
The overall goal of LVA is to create lymphatic-to-venous anterograde flow in as many drainage pathways as possible[48,55-57]. Scenarios of vessel number mismatch, unfavorable pressure gradients, vessel size mismatch, and awkward vessel positioning can be encountered in different combinations. A variety of anastomotic configurations have been developed to overcome such obstacles, named in a lymph-to-vein convention[57-60], as shown in Figure 4.
Figure 4. A variety of anastomotic configurations (named in a lymphatic-to-vein convention) are available to maximize anterograde drainage. (A) Single end-to-end anastomosis, (B) end-to-end anastomosis of two lymphatics to two venous branches, (C) end-to-side anastomosis, (D) depicts multiple small-caliber, fibrotic (non-translucent) lymphatic vessels and a single, large-caliber vein, for which (E) an invaginating “octopus” technique is most appropriate. L: Lymphatic; V: venule.
When lymphatic pressure exceeds venous pressure, all configurations should work; end-to-end will often be chosen as it is the most technically straightforward. However, when the pressure gradient is unfavorable, side-to-side or end-to-side is chosen to take advantage of Bernoulli’s principle[54]. Side-to-side is the more technically challenging and should be performed only if the involved vessels are 0.4 mm or more in diameter. If end-to-end configuration is the only option available due to size limitations, immediate postoperative compression can alter the pressure gradient to facilitate anterograde flow[61].
12-0 nylon on a 50-um needle is generally preferred for anastomosis, but 11-0 nylon can be used for vessels 0.5 mm or larger in diameter. As the vessels are too small for supermicrosurgical forceps tips to insert into the lumen, the needle tip can be used to evert the vessel edge against the side of the forceps[48] with or without the use of a 7-0 monofilament nylon suture acting as an intravascular stent[60,62,63].
After anastomosis, patency is confirmed by washout of the venous lumen by lymphatic fluid[48]. It may not occur immediately after LVA completion due to the slow peristaltic action of lymphatic vessels. Diseased lymphatic vessels may display a particularly delayed washout phenomenon owing to their compromised smooth muscle function. Therefore, anastomoses should be re-assessed several minutes after completion before declaring failure[64]. It can be promoted by massaging distal to incision. Leakproof anastomosis is essential to allow lymphatic pressure to build up and overcome the venous pressure[65]. If the microscope is equipped with an ICG module, patency can be confirmed by observing ICG flow into the veins[65]. If backflow of blood into the lymphatic vessel is observed, venous pressure has exceeded lymphatic pressure, and the anastomosis is at risk of thrombosis.
Controversy exists regarding the optimal number of LVAs[31]. Theoretically, a few high-quality anastomoses (antegrade flow anticipated) should suffice, but reality often necessitates a quantity-over-quality approach. In keeping with this, the senior author (Chen WF) has demonstrated considerable clinical success when using suboptimal vessels by creating 8 to 15 LVAs per case[48,54,64]. The following are used as the procedure endpoints: (1) six hours of operative time; for experienced microsurgeons, continuing beyond this duration typically yields diminishing returns; (2) three consecutive negative incisions (i.e., no suitable lymphatics found when proceeding in a distal-to-proximal fashion); or (3) substantial drainage through LVAs causing visible limb decompression on the table[54].
Frequently refreshing supermicrosurgical skills on practice models can shorten the learning curve for LVA in budding lymphedema surgeons[66].
Technical tips: VLVT
Due to its comparable outcomes and lower invasiveness, SCIP-based VLVT has replaced VLNT as our procedure of choice for those with upper extremity lymphedema who are not LVA candidates. Vascular anatomy is imaged preoperatively with computed tomography angiography or high-resolution duplex ultrasound[67], allowing the more robust-appearing side to be chosen for harvest. Lymphatic vessels are then mapped using ICG imaging after four intradermal injections of 0.05 mL of 0.25% ICG, lateral to the anterior superior iliac spine. Most frequently, the superficial branch of the superficial circumflex iliac artery (SCIA) is selected as the pedicle due to its fast and easy dissection. One should be prepared for occasional anatomic variation necessitating the use of a deep branch. The dissection plane is kept immediately superficial to Scarpa’s fascia, ensuring the exclusion of lymph nodes from the flap and is advanced in a lateral-to-medial direction. It is important to adhere to Scarpa’s fascia during flap elevation and not dissect more superficially as more superficial dissection risks exclusion of the superficial circumflex iliac vein.
The vascular anatomy and perforator location of the TDAP flap is more variable than that of the SCIP flap. Thus, preoperative vascular imaging becomes even more important. Adequate perforators are commonly identifiable with Doppler ultrasound, 8-10 cm inferior to the axillary apex and 1-2 cm inside the lateral border of the latissimus dorsi. Perforators identified in this region may originate from intercostal and lateral thoracic vessels rather than from the thoracodorsal vessel, as shown in Figure 5. However, if adequate pedicle length can be achieved, harvesting the flap on these alternative vessels is acceptable[68,69]. Lymphatics are mapped with intradermal ICG injection of the fifth intercostal space in the midaxillary line to ensure their inclusion in the flap. By dissecting superficial to the superficial fascia, lateral thoracic lymph nodes are excluded from the flap.
Figure 5. Anatomical dissection of the thin TDAP (thoracodorsal artery perforator) flap. The cadaver was pre-injected with red latex to highlight arterial anatomy. (A) Possible sources of skin perforators in the thoracodorsal region. Posterior intercostal vessels, which are another possible source of skin perforators in this region, are not shown here. (B) The perforator was located anterior to the lateral border of the latissimus dorsi muscle. A thin flap was elevated on this perforator, superficial to the superficial fascia. While the descending branch of the TDA is most commonly the source of the TDAP, proximal tracing of this perforator led to the serratus branch of the TDA. However, adequate pedicle length was still achieved. TDA: Thoracodorsal artery; TB: transverse branch of TDA; DBTD: descending branch of TDA; SAB: serratus anterior branch of TDA; LTA: lateral thoracic artery.
For VLVT to be effective, the flap is placed closer to lymphatic edema, and in the proximity of relatively less degenerated lymphatics, both criteria are met in the distal part of the extremity (ankle/wrist). the flap is oriented to match its lymphatics vessels axiality to that of the recipient site lymphatics axiality to allow spontaneous lympholymphatic linkages, as shown by Yamamoto et al.[38]. Just as the minimum number of lymph nodes required for optimum performance of VLNT is not known, the minimum number of lymphatic channels needed for optimum efficacy VLVT is unknown. The density of lymphatic channels in the different flap donor sites has not been experimentally compared, and the minimum size (volume) of the flap required for desirable lymphatic decompression is unclear.
Decision-making: choosing between LVA and VLVT
Both LVA and VLVT are indicated for fluid-predominant lymphedema. Solid predominance, a state of bulky lipodystrophy and fibrosis, should be ruled out clinically (non-pitting edema, no significant volume reduction even after aggressive complex decongestive therapy)[4,70] as well as radiologically with MRI before proceeding.
Misconceptions surrounding LVA have hindered its acceptance amongst surgeons. It is assumed that LVA can only treat early lymphedema and that absence of “linear” patterns on ICG lymphography and/or the presence of venous insufficiency contraindicate its use. Additionally, a few studies have demonstrated inferior outcomes of LVA in lower extremity vs. upper extremity edema, thought to be due to the dependent position and higher venous pressure of the legs[71-75]. Finally, it is also believed that results of LVA take long to become noticeable and are short-lived. In the senior author’s experience, none of the above holds true. The absence of “linear” ICG patterns simply indicates additional effort is needed to locate the lymph vessels, which, once located, are still of sufficient quality to perform LVA. The reduced lymphovenous pressure gradient in the lower extremity can be circumvented with postoperative bandage compression, which creates anterograde flow across the LVAs[53,69,73]. Finally, the senior author has witnessed progressive improvement in patients for as long as 3 years post-surgery, which cannot be explained solely by the mechanical bypass provided by the LVAs. Following the initial lymphatic shunting, possible lymphatic regeneration is hypothesized to play an additional role in ultimately weaning patients off from compression garments.
Recent reports by Yang et al.[76], and growing experience in other high-volume centers has demonstrated that in the hands of experienced supermicrosurgeons, LVA can be successful in moderate-to-severe disease. With the limits of LVA getting pushed further along the spectrum of advanced lymphedema, deciding when to use VLVT instead of LVA becomes less straightforward. VLVT has less associated technical nuances and more predictable outcomes in the hands of less experienced surgeons but requires an additional surgical site. LVA, in contrast, has many technical variables. Even when optimized, its outcomes may not always be predictable. Yet, the minimally invasive nature of LVA outweighs its drawbacks. The success of VLVT depends on the patency of the pedicle anastomosis only, while the success of LVA depends on the quality (patency as well as pressure gradient across the anastomoses) as well as the quantity of the multiple anastomoses (number sufficient to decompress the distended lymphatic system). Discussing this dilemma at length with the patient can help them judiciously weigh the risks and benefits of both procedures and make an informed choice.
Controversy also surrounds the management of primary lymphedema. Many surgeons recommend VLNT over LVA due to theoretical concerns that the abnormal structure and function of lymphatics in these patients may decrease the efficacy of LVA[2,77,78]. However, in our experience, it is not uncommon for patients with primary lymphedema to exhibit global lymphatic dysfunction, as evidenced on ICG lymphography. It precludes any flap transfer procedure in such patients due to an elevated risk of iatrogenic donor-site lymphedema, leaving LVA as a safer alternative[64,79,80].
CONCLUSION
With recent technical refinements in LVA and the evolution of VLVT as a safer alternative to VLNT, outcomes of lymphedema surgery have dramatically improved. The encouraging results of LVA in advanced lymphedema have unveiled its unrealized potential while creating an overlap with the indications of VLVT/VLNT. Though more invasive than LVA, VLVT remains a valuable modality and should be investigated further.
DECLARATIONS
Authors’ contributionsConception and design of the paper: Chen WF
Manuscript writing: Pandey SK, Fahradyan VF, Orfahli LM, Chen WF
Final approval of manuscript: Pandey SK, Fahradyan VF, Orfahli LM, Chen WF
Availability of data and materialsNot applicable.
Financial support and sponsorshipNone.
Conflicts of interestAll authors declared that there are no conflicts of interest.
Ethical approval and consent to participateNot applicable.
Consent for publicationWritten informed consent for publication of de-identified images was obtained.
Copyright© The Author(s) 2021.
REFERENCES
1. Torrisi JS, Joseph WJ, Ghanta S, et al. Lymphaticovenous bypass decreases pathologic skin changes in upper extremity breast cancer-related lymphedema. Lymphat Res Biol 2015;13:46-53.
2. Garza RM, Chang DW. Lymphovenous bypass for the treatment of lymphedema. J Surg Oncol 2018;118:743-9.
3. Basta MN, Gao LL, Wu LC. Operative treatment of peripheral lymphedema: a systematic meta-analysis of the efficacy and safety of lymphovenous microsurgery and tissue transplantation. Plast Reconstr Surg 2014;133:905-13.
5. Koshima I, Narushima M, Mihara M, et al. Lymphadiposal flaps and lymphaticovenular anastomoses for severe leg edema: functional reconstruction for lymph drainage system. J Reconstr Microsurg 2016;32:50-5.
6. Orfahli LM, Fahradyan V, Chen WF. Vascularized lymph vessel transplant (VLVT): our experience and lymphedema treatment algorithm. Ann Breast Surg 2021; doi: 10.21037/abs-20-139.
7. Chen WF, Mcnurlen M, Ding J, Bowen M. Vascularized lymph vessel transfer for extremity lymphedema - is transfer of lymph node still necessary? IMJ 2019;3:1.
8. Allen RJ Jr, Cheng MH. Lymphedema surgery: patient selection and an overview of surgical techniques. J Surg Oncol 2016;113:923-31.
10. Chang TS, Yu HL, Wei W, Huang WY. Microsurgery for lymphedema and lymphatics. Principles, Techniques and Applications in Microsurgery. WORLD SCIENTIFIC; 1986. p. 331-62.
11. Gilbert A, O'brien B, Vorrath J, Sykes P. Lymphaticovenous anastomosis by microvascular technique. Br J Plast Surg 1976;29:355-60.
12. Yamada Y. The studies on lymphatic venous anastomosis in lvmphedema. Nagoya J Med Sci 1969;32:1-21.
13. Nielubowicz J, Olszewski W. Surgical lymphaticovenous shunts in patients with secondary lymphoedema. Br J Surg 1968;55:440-2.
15. O'Brien BM, Sykes P, Threlfall GN, Browning FS. Microlymphaticovenous anastomoses for obstructive lymphedema. Plast Reconstr Surg 1977;60:197-211.
16. Mihara M, Hara H, Hayashi Y, et al. Pathological steps of cancer-related lymphedema: histological changes in the collecting lymphatic vessels after lymphadenectomy. PLoS One 2012;7:e41126.
17. Mihara M, Hara H, Kawakami Y, et al. Site specific evaluation of lymphatic vessel sclerosis in lower limb lymphedema patients. Lymphat Res Biol 2018;16:360-7.
18. Koshima I, Kawada S, Moriguchi T, Kajiwara Y. Ultrastructural observations of lymphatic vessels in lymphedema in human extremities. Plast Reconstr Surg 1996;97:397-405; discussion 406-7.
19. Koshima I, Inagawa K, Urushibara K, Moriguchi T. Supermicrosurgical lymphaticovenular anastomosis for the treatment of lymphedema in the upper extremities. J Reconstr Microsurg 2000;16:437-42.
20. Nagase T, Gonda K, Inoue K, et al. Treatment of lymphedema with lymphaticovenular anastomoses. Int J Clin Oncol 2005;10:304-10.
21. Shesol BF, Nakashima R, Alavi A, Hamilton RW. Successful lymph node transplantation in rats, with restoration of lymphatic function. Plast Reconstr Surg 1979;63:817-23.
22. Chen H, O'brien B, Rogers I, Pribaz J, Eaton C. Lymph node transfer for the treatment of obstructive lymphoedema in the canine model. Br J Plast Surg 1990;43:578-86.
23. Cheng MH, Huang JJ, Wu CW, et al. The mechanism of vascularized lymph node transfer for lymphedema: natural lymphaticovenous drainage. Plast Reconstr Surg 2014;133:192e-8e.
24. Honkonen KM, Visuri MT, Tervala TV, et al. Lymph node transfer and perinodal lymphatic growth factor treatment for lymphedema. Ann Surg 2013;257:961-7.
25. Schaverien MV, Badash I, Patel KM, Selber JC, Cheng MH. Vascularized lymph node transfer for lymphedema. Semin Plast Surg 2018;32:28-35.
26. Saaristo AM, Niemi TS, Viitanen TP, Tervala TV, Hartiala P, Suominen EA. Microvascular breast reconstruction and lymph node transfer for postmastectomy lymphedema patients. Ann Surg 2012;255:468-73.
27. Ito R, Zelken J, Yang CY, Lin CY, Cheng MH. Proposed pathway and mechanism of vascularized lymph node flaps. Gynecol Oncol 2016;141:182-8.
28. Suami H, Scaglioni MF, Dixon KA, Tailor RC. Interaction between vascularized lymph node transfer and recipient lymphatics after lymph node dissection-a pilot study in a canine model. J Surg Res 2016;204:418-27.
29. Patel KM, Lin CY, Cheng MH. From theory to evidence: long-term evaluation of the mechanism of action and flap integration of distal vascularized lymph node transfers. J Reconstr Microsurg 2015;31:26-30.
30. Pappalardo M, Patel K, Cheng MH. Vascularized lymph node transfer for treatment of extremity lymphedema: An overview of current controversies regarding donor sites, recipient sites and outcomes. J Surg Oncol 2018;117:1420-31.
31. Hanson SE, Chang EI, Schaverien MV, Chu C, Selber JC, Hanasono MM. Controversies in surgical management of lymphedema. Plast Reconstr Surg Glob Open 2020;8:e2671.
32. Chang EI, Chu CK, Hanson SE, Selber JC, Hanasono MM, Schaverien MV. Comprehensive overview of available donor sites for vascularized lymph node transfer. Plast Reconstr Surg Glob Open 2020;8:e2675.
33. Ciudad P, Agko M, Perez Coca JJ, et al. Comparison of long-term clinical outcomes among different vascularized lymph node transfers: 6-year experience of a single center's approach to the treatment of lymphedema. J Surg Oncol 2017;116:671-82.
34. Coriddi M, Wee C, Meyerson J, Eiferman D, Skoracki R. Vascularized jejunal mesenteric lymph node transfer: a novel surgical treatment for extremity lymphedema. J Am Coll Surg 2017;225:650-7.
35. Gustafsson J, Chu SY, Chan WH, Cheng MH. Correlation between quantity of transferred lymph nodes and outcome in vascularized submental lymph node flap transfer for lower limb lymphedema. Plast Reconstr Surg 2018;142:1056-63.
36. Garcés M, Pons G, Mirapeix R, Masià J. Intratissue lymphovenous communications in the mechanism of action of vascularized lymph node transfer. J Surg Oncol 2017;115:27-31.
37. Ito R, Suami H. Overview of lymph node transfer for lymphedema treatment. Plast Reconstr Surg 2014;134:548-56.
38. Yamamoto T, Iida T, Yoshimatsu H, Fuse Y, Hayashi A, Yamamoto N. Lymph flow restoration after tissue replantation and transfer: importance of lymph axiality and possibility of lymph flow reconstruction without lymph node transfer or lymphatic anastomosis. Plast Reconstr Surg 2018;142:796-804.
39. Slavin SA, Upton J, Kaplan WD, Van den Abbeele AD. An investigation of lymphatic function following free-tissue transfer. Plast Reconstr Surg 1997;99:730-41; discussion 742-3.
40. Scallan JP, Zawieja SD, Castorena-Gonzalez JA, Davis MJ. Lymphatic pumping: mechanics, mechanisms and malfunction. J Physiol 2016;594:5749-68.
41. Chen WF, Zhao H, Yamamoto T, Hara H, Ding J. Indocyanine green lymphographic evidence of surgical efficacy following microsurgical and supermicrosurgical lymphedema reconstructions. J Reconstr Microsurg 2016;32:688-98.
42. Hawkes PJ, Mcnurlen M, Bowen M, Chen WF. Strategic incision placement to facilitate successful supermicrosurgical lymphaticovenular anastomoses. IMJ 2018;1:5.
43. Cha HG, Oh TM, Cho MJ, et al. Changing the paradigm: lymphovenous anastomosis in advanced stage lower extremity lymphedema. Plast Reconstr Surg 2021;147:199-207.
44. Hayashi A, Giacalone G, Yamamoto T, et al. Ultra high-frequency ultrasonographic imaging with 70 MHz scanner for visualization of the lymphatic vessels. Plast Reconstr Surg Glob Open 2019;7:e2086.
45. Cheng MH, Al-Jindan FK, Lin CY. Abstract: comparison of outcomes between side-to-end and end-to-end lymphovenous anastomoses for early-grade extremity lymphedema. Plast Reconstr Surg Glob Open 2018;6:56.
46. AlJindan FK, Lin CY, Cheng MH. Comparison of outcomes between side-to-end and end-to-end lymphovenous anastomoses for early-grade extremity lymphedema. Plast Reconstr Surg 2019;144:486-96.
47. Mihara M, Hara H, Tange S, et al. Multisite Lymphaticovenular bypass using supermicrosurgery technique for lymphedema management in lower lymphedema cases. Plast Reconstr Surg 2016;138:262-72.
48. Chen WF. How to get started performing supermicrosurgical lymphaticovenular anastomosis to treat lymphedema. Ann Plast Surg 2018;81:S15-20.
49. Mihara M, Hara H, Kikuchi K, et al. Scarless lymphatic venous anastomosis for latent and early-stage lymphoedema using indocyanine green lymphography and non-invasive instruments for visualising subcutaneous vein. J Plast Reconstr Aesthet Surg 2012;65:1551-8.
50. Mihara M, Hara H, Hayashi Y, et al. Upper-limb lymphedema treated aesthetically with lymphaticovenous anastomosis using indocyanine green lymphography and noncontact vein visualization. J Reconstr Microsurg 2012;28:327-32.
51. Belgrado JP, Vandermeeren L, Vankerckhove S, et al. Near-infrared fluorescence lymphatic imaging to reconsider occlusion pressure of superficial lymphatic collectors in upper extremities of healthy volunteers. Lymphat Res Biol 2016;14:70-7.
52. Pan WR, Wang DG, Levy SM, Chen Y. Superficial lymphatic drainage of the lower extremity: anatomical study and clinical implications. Plast Reconstr Surg 2013;132:696-707.
53. Hara H, Mihara M, Seki Y, Todokoro T, Iida T, Koshima I. Comparison of indocyanine green lymphographic findings with the conditions of collecting lymphatic vessels of limbs in patients with lymphedema. Plast Reconstr Surg 2013;132:1612-8.
54. Chen WF, Tuncer FB, Zeng W. Advanced technical pearls for successful supermicrosurgical lymphaticovenular anastomosis. Ann Plast Surg 2021;86:S165-72.
55. Matsutani H, Hayashi A, Yamamoto T. All-star lymphatic supermicrosurgery: Multiple lymph flow diversion using end-to-end, end-to-side, side-to-end, and side-to-side lymphaticovenular anastomoses in a surgical field. J Plast Reconstr Aesthet Surg 2015;68:e107-8.
56. Yamamoto T, Furuya M, Harima M, Hayashi A, Koshima I. Triple supermicrosurgical side-to-side lymphaticolymphatic anastomoses on a lymphatic vessel end-to-end anastomosed to a vein. Microsurgery 2015;35:249-50.
57. Yamamoto T, Kikuchi K, Yoshimatsu H, Koshima I. Ladder-shaped lymphaticovenular anastomosis using multiple side-to-side lymphatic anastomoses for a leg lymphedema patient. Microsurgery 2014;34:404-8.
58. Chen WF, Yamamoto T, Fisher M, Liao J, Carr J. The "Octopus" lymphaticovenular anastomosis: evolving beyond the standard supermicrosurgical technique. J Reconstr Microsurg 2015;31:450-7.
59. Yamamoto T, Chen WF, Yamamoto N, Yoshimatsu H, Tashiro K, Koshima I. Technical simplification of the supermicrosurgical side-to-end lymphaticovenular anastomosis using the parachute technique. Microsurgery 2015;35:129-34.
60. Yamamoto T, Narushima M, Kikuchi K, et al. Lambda-shaped anastomosis with intravascular stenting method for safe and effective lymphaticovenular anastomosis. Plast Reconstr Surg 2011;127:1987-92.
61. Chen WF, Bowen M, Ding J. Immediate limb compression following supermicrosurgical lymphaticovenular anastomosis - is it helpful or harmful? IMJ 2018;2:1.
62. Yamamoto T, Yoshimatsu H, Narushima M, Yamamoto N, Koshima I. Split intravascular stents for side-to-end lymphaticovenular anastomosis. Ann Plast Surg 2013;71:538-40.
63. Nuri T, Ueda K, Yamada A, Hara M. Preparatory intravascular stenting technique: an easier method of supermicrosurgical lymphaticovenular anastomosis. Ann Plast Surg 2013;71:541-3.
64. Chen WF, McNurlen M, Bowen M. Surgical treatments of lymphedema. In: Jones GE, editor. Bostwick’s plastic and reconstructive breast surgery. Thieme Medical Publishers; 2020. p. 1478-99.
65. Hayashi A, Yoshimatsu H, Visconti G, et al. Intraoperative real-time visualization of the lymphatic vessels using microscope-integrated laser tomography. J Reconstr Microsurg 2021;37:427-35.
66. Chen WF, Eid A, Yamamoto T, Keith J, Nimmons GL, Lawrence WT. A novel supermicrosurgery training model: the chicken thigh. J Plast Reconstr Aesthet Surg 2014;67:973-8.
67. Visconti G, Bianchi A, Hayashi A, et al. Thin and superthin perforator flap elevation based on preoperative planning with ultrahigh-frequency ultrasound. Arch Plast Surg 2020;47:365-70.
68. Jain L, Kumta SM, Purohit SK, Raut R. Thoracodorsal artery perforator flap: indeed a versatile flap. Indian J Plast Surg 2015;48:153-8.
69. Kim KN, Hong JP, Park CR, Yoon CS. Modification of the elevation plane and defatting technique to create a thin thoracodorsal artery perforator flap. J Reconstr Microsurg 2016;32:142-6.
70. Brorson H, Svensson H. Liposuction combined with controlled compression therapy reduces arm lymphedema more effectively than controlled compression therapy alone. Plast Reconstr Surg 1998;102:1058-67.
71. Forte AJ, Khan N, Huayllani MT, et al. Lymphaticovenous anastomosis for lower extremity lymphedema: a systematic review. Indian J Plast Surg 2020;53:17-24.
72. Qiu SS, Pruimboom T, Cornelissen AJM, Schols RM, van Kuijk SMJ, van der Hulst RRWJ. Outcomes following lymphaticovenous anastomosis (LVA) for 100 cases of lymphedema: results over 24-months follow-up. Breast Cancer Res Treat 2020;184:173-83.
73. Chang DW, Suami H, Skoracki R. A prospective analysis of 100 consecutive lymphovenous bypass cases for treatment of extremity lymphedema. Plast Reconstr Surg 2013;132:1305-14.
74. Chung JH, Baek SO, Park HJ, Lee BI, Park SH, Yoon ES. Efficacy and patient satisfaction regarding lymphovenous bypass with sleeve-in anastomosis for extremity lymphedema. Arch Plast Surg 2019;46:46-56.
75. Hara H, Mihara M. Lymphaticovenous anastomosis for advanced-stage lower limb lymphedema. Microsurgery 2021;41:140-5.
76. Yang JC, Wu SC, Lin WC, Chiang MH, Chiang PL, Hsieh CH. Supermicrosurgical lymphaticovenous anastomosis as alternative treatment option for moderate-to-severe lower limb lymphedema. J Am Coll Surg 2020;230:216-27.
77. Mihara M, Hara H, Furniss D, et al. Lymphaticovenular anastomosis to prevent cellulitis associated with lymphoedema. Br J Surg 2014;101:1391-6.
78. Drobot A, Bez M, Abu Shakra I, et al. Microsurgery for management of primary and secondary lymphedema. J Vasc Surg Venous Lymphat Disord 2021;9:226-33.e1.
79. Giacalone G, Yamamoto T, Belva F, et al. The application of virtual reality for preoperative planning of lymphovenous anastomosis in a patient with a complex lymphatic malformation. J Clin Med 2019;8:371.
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Pandey SK, Fahradyan V, Orfahli LM, Chen WF. Supermicrosurgical lymphaticovenular anastomosis vs. vascularized lymph vessel transplant - technical optimization and when to perform which. Plast Aesthet Res 2021;8:47. http://dx.doi.org/10.20517/2347-9264.2021.61
AMA Style
Pandey SK, Fahradyan V, Orfahli LM, Chen WF. Supermicrosurgical lymphaticovenular anastomosis vs. vascularized lymph vessel transplant - technical optimization and when to perform which. Plastic and Aesthetic Research. 2021; 8: 47. http://dx.doi.org/10.20517/2347-9264.2021.61
Chicago/Turabian Style
Pandey, Sonia Kukreja, Vahe Fahradyan, Lynn M. Orfahli, Wei F. Chen. 2021. "Supermicrosurgical lymphaticovenular anastomosis vs. vascularized lymph vessel transplant - technical optimization and when to perform which" Plastic and Aesthetic Research. 8: 47. http://dx.doi.org/10.20517/2347-9264.2021.61
ACS Style
Pandey, SK.; Fahradyan V.; Orfahli LM.; Chen WF. Supermicrosurgical lymphaticovenular anastomosis vs. vascularized lymph vessel transplant - technical optimization and when to perform which. Plast. Aesthet. Res. 2021, 8, 47. http://dx.doi.org/10.20517/2347-9264.2021.61
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