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Case Reports in Medicine
Volume 2012 (2012), Article ID 648683, 4 pages
Treatment of Chronic Posttraumatic Leg Injury Using Autologous Fat Graft
1U.O.C. Chirurgia Plastica, IRCCS Multimedica, Università Degla Studi di Milano, Sesto San Giovanni, 20089 Rozzano, Milano, Italy
2U.O. Chirurgia Plastica 2, Dipartimento di Medicina Traslazionale, Università Degli Studi di Milano e IRCCS Istituto Clinico Humanitas, 20089 Rozzano, Milano, Italy
Received 20 September 2012; Accepted 6 December 2012
Academic Editor: Jeffrey C. Wang
Copyright © 2012 Fabio Caviggioli et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
We present the results obtained in a case of a 20-year-old Caucasian woman with a posttraumatic injury “hard-to-heal” of the left leg treated using autologous fat graft. Considering our experience in treatment of chronic posttraumatic ulcers by autologous fat graft, we decided to use this surgical technique to induce a regenerative effect in this young patient. We have had complete wound closure with only a single surgical procedure after 1 month; after the second intervention of autologous fat graft we observed an improvement in the quality of the scar tissue. The patient satisfaction was excellent. The results were long lasting and remained virtually unchanged after 1 year.
In the last 10 years autologous fat graft has become a surgical technique used in many fields; we applied this technique to scars with improvement of mimic features, skin texture, softness, and thickness; to treat radio damaged tissues, hard-to-heal wound, posttraumatic ulcers, chronic pain syndrome, and in aesthetic surgery [1–12]. We present the results obtained in treatment in a case of posttraumatic ulcer using fat graft.
2. Case Reports
An 18-year-old Caucasian woman was refered to our attention for a posttraumatic injury at the left leg; the patient reported to have had a traffic accident two months before the first clinical evaluation, with extensive loss of soft tissue at distal third region of left leg, peroneal nerve injury, and exposure of tendons.
During our first clinical evaluation we described two ulcers at distal third level of the left leg that appeared well, cleaned without macroscopic signs of infection. The wounds size was about 7.5 cm to 4 cm in diameter for the first and 3 cm to 3 cm for the second injury (Figure 1). The patient reported that leg ulcers were treated with topical therapies including regular dressing changes, wound cleansers, and advanced dressing with no wound healing improvement or ulcers resolution.
Initially we have decided to treat the lesion using an Ollier-Thiersch dermoepidermal graft harvested at the level of the inner face of the ipsilateral thigh. This intervention has resulted in resolution of minor wound and only partial improvement of the major lesion in the left leg; three months after surgical procedure we did not observe spontaneous wound healing improvement (Figure 2). Considering our experience in treatment of chronic post traumatic ulcers by autologous fat graft, we decided to use this surgical technique to induce a regenerative effect in this young patient.
2.1. Preoperative Planning
The patient was healthy, without home therapy and nonsmoker.
After standard blood examination and electrocardiography we performed surgical treatment.
Antibiotic prophylaxis (cefazolin 2 g 30 minutes before the intervention) is administered.
2.2. Surgical Procedure
Our goal is to obtaine a full reepithelization of the ulcer using the regenerative potential of autologous fat graft. The surgical procedure is performed under local anesthesia and sedation assisted with sterile technique. Abdomen area represents the donor sites selected for the easy access to the patient in supine position, for the abundant reserves of adipose tissue, and the absence of postoperative outcomes. After the preliminary incision of the skin with a scalpel blade n°11, we proceed to infiltration of the donor areas, at the level of deep subcutaneous tissue, using a blunt cannula filled with a particular anesthetic solution (100 mL saline solution, 10 mL of levobupivacaine 7.5 mg/mL, 20 mL of mepivacaine 10 mg/mL, and 0.5 mL epinephrine 1 mg/mL). Infiltration provides good hemostasis and adequate operative and perioperative analgesic action. Adipose tissue is harvested through the same incision for infiltration of anesthetic solution, with blunt cannulae of 2-3 mm of diameter of variable length (between 15 and 23 cm). The cannula used for sampling is connected with a Luer-lock syringe of 10 cc. The syringe plunger is pulled at the top and secured with a “Backhaus” clamp. This creates, inside the syringe, a slight negative pressure which allows the levy of adipose tissue, while the cannula is advanced and retracted with radial movements inside the donor area. When the syringe is full, it is closed using a Luer-lock cap to prevent loss of content and the syringe plunger is removed. The syringe is now placed in a centrifuge with resterilized containers and adipose tissue is processed following Coleman’s technique (i.e., centrifugated at 3,000 rpm for 3 minutes).
We prefer to harvest fat at the level of deep subcutaneous tissue to avoid risk of skin retraction.
After the centrifugation we obtain, inside the syringe, three distinct layers. The top layer, which is the less dense one, is made of oil derived from the breakdown of fat cells; in the intermediate portion we find adipocytes and stromal-vascular tissue; in the lower level, the denser one, we find damaged blood cells, water, and anesthetic mixture. As the only layer that we need for the therapeutic purpose is the intermediate one, the oily layer is absorbed by tissue strips, and the lower layer is removed by removing the cap from the syringe, in this way permitting the spontaneous drainage of the aqueous portion. Fat is transferred from a 10 mL syringe in a 1 mL syringe Luer-lock that allows precise control of the amount of injected fat and better handling. The adipocyte fraction is injected using an 18-gauge angiographic needle with a snap-on wing (by Cordis, a Johnson & Johnson Company, N.V, 9301 LJ Roden, The Netherlands).
The adipose tissue fraction has been deposited at the dermal-hypodermal junction in the ulcer’s edges with the use of small syringes described above; in addition, fat is grafted into the wound bed. Through the same incision many radiating passages are made, to have fat in different directions according to an ideal form of web to support damaged areas. This technique seems to allow better fat graft survival, to increases rooting and to minimize the possibility of forming cavities filled with triglycerides. The amount of tissue grafted depends on the extension of scar that we need to treat; usually we inject about 1 mL for an area of 2.5 cm2 scar surface. In this case we have injected about 5 mL of centrifuged adipose tissue (about 4.5 mg of fat).
The amount of injected fat at each passage is minimized to avoid irregularities and clusters, which are eventually deleted with digital manipulation after procedure. Injection is performed with retrograde technique leaving a very small space between the injected tissue lines.
The access incisions in the donor areas are sutured with nylon 3/0.
A second grafting session of the same volume of graft was performed 6 months later to improve the depth and appearance of the scar tissue.
The treated area after surgical debridement was covered with calcium alginate dressing and gauze fixed using paper patches for 1 week and it is recommended to the patient to avoid pressure and friction to limit the displacement of fat infiltration
At the harvest site level we applied self-adhering open cell foam dressing fixed with an elastic adhesive bandaging which has to be kept in place for 5 days. This type of dressing allow us to prevent hematomas and local fibrosis.
2.4. Postoperative Care
Postoperative paracetamol 1 g/8 h is administered. The patient was monitored for 4 hours after surgery to early identify any local bleeding or systemic symptoms of postoperative discomfort.
The patient is discharged on the same day. Outpatient therapy includes cefixime 400 mg/day for 5 days, paracetamol 500 mg if pain or fever. An ambulatory monitoring was programmed seven days after surgery.
The dressing is removed 7 days after surgery. The patient has to come to clinical assessment at 1 week, 2 weeks, 1 month, 3, 6, and 12 months.
The outcome at 3 months and 12 months after first autologous fat graft can be seen in Figures 3 and 4. We have had complete wound closure with only a single surgical procedure after 1 month; 12 months after first fat graft (6 months after second grafting session) we observed an improvement in the quality of the scar tissue. The patient satisfaction was excellent.
In this paper we showed a complete wound healing in a case of hard-to-heal post traumatic ulcer. The results, already evident at four weeks after surgery, were long lasting and remained virtually unchanged after 1 year.
Since the volume injected by lipostructure is small, even the early results of this procedure can be hardly due to a “filler effect” and suggest that deep biological interactions between transplanted fat and dermal-subdermal structures occur very soon. The rapid improvement of wound healing process and complete recovery of tissue integrity after surgery seems to confirm the regenerative effect of fat graft. Moreover, we have observed an improvement of healed skin quality and elasticity, that appears very similar to normal skin after second fat graft.
Firstly in 2001, Zuk et al. demonstrated the existence of adipose tissue-derived stem cells ; then, other studies attempted to discover the operating mechanism of adipose tissue in the regenerative process [14, 15] and the application of its components in different therapies, including regenerative medicine and tissue engineering [16, 17].
The presence of adult mesenchymal stem cells represents an element of great importance for reshaping tissue and increase the quality and elasticity, as observed in the case described.
Although regenerative mechanisms of fat graft are not fully understood, hypoxia could play an important role because it represents an important stimulus for the production of growth factors and neoangiogenesis that facilitating healing.
Lipostructure with Coleman’s technique is reported to be a safe, rapid, and effective procedure.
It is becoming increasingly popular in aesthetic surgery and its range of indications is widening.
In particular, ulcers treatment by lipostructure is being yielded encouraging results and, in our opinion in the future, will allow to make the application suitable to all types of ulcers (posttraumatic, vascular, and pressure ulcers), especially if no alternative procedure is available.
- M. Klinger, M. Marazzi, D. Vigo, and M. Torre, “Fat injection for cases of severe burn outcomes: a new perspective of scar remodeling and reduction,” Aesthetic Plastic Surgery, vol. 32, no. 3, pp. 465–469, 2008.
- F. Caviggioli, F. Klinger, D. Forcellini et al., “Scar treatment by lipostructure,” Update in Plastic Surgery, vol. 2, pp. 51–53, 2009.
- F. Caviggioli, F. Klinger, F. Villani, C. Fossati, V. Vinci, and M. Klinger, “Correction of cicatricial ectropion by autologous fat graft,” Aesthetic Plastic Surgery, vol. 32, no. 3, pp. 555–557, 2008.
- M. Klinger, F. Caviggioli, V. Vinci, A. Salval, and F. Villani, “Treatment of chronic posttraumatic ulcers using autologous fat graft,” Plastic and Reconstructive Surgery, vol. 126, no. 3, pp. 154e–155e, 2010.
- F. Caviggioli, F. Villani, D. Forcellini, V. Vinci, and F. Klinger, “Nipple resuscitation by lipostructure in burn sequelae and scar retraction,” Plastic and Reconstructive Surgery, vol. 125, no. 4, pp. 174–176, 2010.
- F. Caviggioli, S. Giannasi, V. Vinci, G. Cornegliani, D. Levi, and P. Gaetani, “Five-year outcome of surgical treatment of migraine headaches,” Plastic and Reconstructive Surgery, vol. 128, no. 5, pp. 564e–565e, 2011.
- F. Caviggioli, D. Forcellini, V. Vinci, G. Cornegliani, F. Klinger, and M. Klinger, “Employment of needles: a different technique for fat placement,” Plastic and Reconstructive Surgery, vol. 130, pp. 373e–374e, 2012.
- F. Caviggioli, L. Maione, V. Vinci, and M. Klinger, “The most current algorithms for the treatment and prevention of hypertrophic scars and keloids,” Plastic and Reconstructive Surgery, vol. 126, no. 3, pp. 1130–1131, 2010.
- F. Caviggioli, V. Vinci, A. Salval, and M. Klinger, “Human adipose-derived stem cells: isolation, characterization and applications in surgery,” ANZ Journal of Surgery, vol. 79, no. 11, p. 856, 2009.
- F. M. Klinger, F. Caviggioli, D. Forcellini et al., “Breast fistula repair after autologous fat graft: a case report,” Case Reports in Medicine, vol. 2011, Article ID 547387, 3 pages, 2011.
- F. Villani, F. Caviggioli, F. Klinger, L. Maione, and M. Klinger, “Fat graft before breast reconstruction by Latissimus Dorsi,” Plastic and Reconstructive Surgery, vol. 126, no. 4, pp. 190e–192e, 2010.
- F. Caviggioli, L. Maione, D. Forcellini, F. Klinger, and M. Klinger, “Autologous fat graft in postmastectomy pain syndrome,” Plastic and Reconstructive Surgery, vol. 128, pp. 349–352, 2011.
- P. A. Zuk, M. Zhu, H. Mizuno et al., “Multilineage cells from human adipose tissue: implications for cell-based therapies,” Tissue Engineering, vol. 7, no. 2, pp. 211–228, 2001.
- J. M. Gimble and M. E. Nuttall, “Bone and fat: old questions, new insights,” Endocrine, vol. 23, no. 2-3, pp. 183–188, 2004.
- H. X. Li, X. Luo, R. X. Liu, Y. J. Yang, and G. S. Yang, “Roles of Wnt/β-catenin signaling in adipogenic differentiation potential of adipose-derived mesenchymal stem cells,” Molecular and Cellular Endocrinology, vol. 291, no. 1-2, pp. 116–124, 2008.
- R. S. Tiǧli, S. Ghosh, M. M. Laha et al., “Comparative chondrogenesis of human cell sources in 3D scaffolds,” Journal of Tissue Engineering and Regenerative Medicine, vol. 3, no. 5, pp. 348–360, 2009.
- J. Lin, M. L. Lindsey, B. Zhu, C. M. Agrawal, and S. R. Bailey, “Effects of surface-modified scaffolds on the growth and differentiation of mouse adipose-derived stromal cells,” Journal of Tissue Engineering and Regenerative Medicine, vol. 1, no. 3, pp. 211–217, 2007.