Treatment of Postsurgical Scalp Scar Deformity Using Follicular Unit Hair Transplantation

Yoo, Hyokyung; Moh, Jaeseong; Park, Ji-Ung

doi:https://doi.org/10.1155/2019/3423657

BioMed Research International

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Abstract Introduction Materials and Methods Results Discussion Conclusions Data Availability Ethical Approval Disclosure Conflicts of Interest References Copyright Related Articles

Clinical Study | Open Access

Volume 2019 | Article ID 3423657 | https://doi.org/10.1155/2019/3423657

Treatment of Postsurgical Scalp Scar Deformity Using Follicular Unit Hair Transplantation

Hyokyung Yoo,¹Jaeseong Moh,²and Ji-Ung Park¹

Academic Editor: Giulio Gasparini

Received29 Mar 2019

Accepted23 Apr 2019

Published13 May 2019

Abstract

Background. Although stable cicatricial alopecia (SCA) secondary to surgical events of the scalp can affect patients’ psychosocial status, hair transplantation onto postsurgical scar tissue on the scalp is challenging because of tissue stiffness and poor blood circulation. Objective. In contrast to traditional surgical treatments, such as excision, local flap, and tissue expansion, follicular unit (FU) hair transplantation offers aesthetically pleasing results in the treatment of postsurgically induced SCA. Materials and Methods. This study included 15 patients with SCA of the scalp due to postsurgical scarring. The patients underwent a single session of hair transplantation of approximately 35 units/cm² density. The graft survival rate was evaluated 12 months after the procedure. The Patient and Observer Scar Assessment Scale (POSAS) was used to analyze the preoperative and postoperative satisfaction. Results. The FUE hair transplantation had a mean survival rate of 80.67% (range 70-90%). The patient and observer satisfaction significantly improved after the procedure; the POSAS scores were 24.47 (range 16-38) preoperatively and 11.60 (range 7-18) postoperatively. Conclusion. FU hair transplantation could be an effective method for managing scar tissue on the scalp and offers several advantages, including a high transplantation survival rate and satisfactory postoperative results.

1. Introduction

Because hair plays an important role in an individual’s social and psychological health, maintaining and preventing hair loss are major concerns of individuals of various ages and genders. Due to growing interest in and demand for cosmetic procedures, range has been broadened from male pattern baldness to different types of alopecia, such as hairline correction in women and sideburn grafts.

According to Unger, hairless lesions secondary to traumatic events (e.g., burns, radiation, prior surgeries, and traction injuries) that can cause permanent scarring in a hair-bearing region are specifically called “stable cicatricial alopecia (SCA)” [1]. Due to the general popularity of facial cosmetic surgeries, such as forehead lifts, forehead implants, and fat grafts, and the increasing numbers of complications involving scalp scars following these operations, there is an increased demand for the treatment of postsurgical alopecia [2–5].

For the most common nonscarring alopecias, such as androgenetic alopecia or alopecia areata, several effective medical treatments have been developed, such as oral finasteride and topical minoxidil [6–8]. Surgical treatment options also exist, including tissue expansion, flap surgery, and hair transplantation; all of these procedures are widely performed with successful results [9–12].

However, many surgeons have found the surgical treatment of traumatic or postsurgical cicatricial alopecia challenging because of tissue stiffness, possible poor blood circulation, and infection. As a result, the excision and direct closure method is preferred over hair transplantation as the primary surgical modality for correcting small alopecia lesions. However, the excisional method often leaves wide scars that widen further due to secondary tension [13–16].

Surgical treatment for postsurgical scar deformity is rarely performed and has been ignored. However, the treatment of even small hairless areas of postsurgical SCA cannot be ignored because these areas can become sources of psychosocial alienation and dissatisfaction [17, 18]. We introduce an effective surgical method for managing postoperative small SCA areas using follicular unit (FU) hair transplantatio, and present a series of cases with aesthetically pleasing outcomes.

2. Materials and Methods

From December 2013 to August 2016, 15 patients with postsurgical SCA were included in the study. All patients had scar-induced hairless lesions on their scalps caused by various operations, including forehead implant insertion (n=2), Endotine (Endotine™ forehead bioabsorbable implant, MicroAire Aesthetics, Charlottesville, VA, USA) lift (n=2), previous hair transplantation donor sites (n=5), forehead reduction (n=1), fat grafting (n=1), nevus excision (n=1), and neurosurgeries (n=3). Follicular units were harvested from the occipital area by the strip excision (n=4) or follicular unit extraction (FUE) technique (n=11) using an electronic punch device (Folligraft®, LeadM Corp., Seoul, Republic of Korea) and placed onto the recipient site at the scalp using a hair implanter (Choi Implanter, LeadM Corp., Seoul, Republic of Korea). The affected scarred area on the scalp was calculated by tracing the lesion on millimeter graded transparent paper. Because the desired FU density of the recipient site was approximately 35 units/cm², we could determine the approximate number of FUs to harvest by multiplying the calculated recipient area by the desired density (35 FU/cm²).

No additional procedures were performed after the transplantation operations, and all the patients completed their treatment in only one procedural session. Oral antibiotics were administered for 3 postoperative days, and no occlusive dressing was needed except immediate compression of the recipient site and donor site for up to 30 minutes. The patients were able to wash their hair 24 hours after the procedure.

The patients were scheduled to visit the clinic 12 months after the operations so that the graft survival rate could be determined. The Patient and Observer Scar Assessment Scale (POSAS), a promising scar evaluation tool involving both the observer’s and the patient’s perspectives, was applied for each patient to objectively assess satisfaction. All procedures in the present study were performed in accordance with the Declaration of Helsinki, and approval was granted by the Institutional Review Board of the Seoul National University Boramae Medical Center (IRB No. 10-2018-6).

2.1. Surgical Procedure

First, the donor and recipient sites were anesthetized by regional block involving the supraorbital, supratrochlear, and occipital nerves with a mixture of 2% lidocaine and 1:1000 epinephrine. Following nerve blockage, Abbasi solution comprising 100 ml of 0.9% normal saline solution, 5.0 ml of 2% lidocaine, 1 ml of 1:1,000 epinephrine, and 1.0 ml triamcinolone 40 mg/ml was infiltrated throughout the donor and recipient sites [19].

In cases of more than 500 FUs, we performed occipital scalp strip excision (2 to 3 cm wide and 13 to 20 cm long) and extracted the FUs for transplantation. If a small number of less than 500 FUs were needed, we extracted individual FUs using an electronic circular punch with a blunt tip and a diameter of 0.8 mm. The instrument’s blunt tip reduced damage to the follicles, and the small holes created by the punch healed within a few days by secondary healing. The extracted FUs were handled gently and kept moist in 0.9% normal saline as the holding solution until they were transplanted. The FUs were sorted by the number of hairs and their thickness such that they could be selectively grafted to appropriate areas of the scalp. The FU grafts were transplanted using a manual implanter with an average density of 35 units/cm² [20–22].

2.2. Patient and Observer Scar Assessment Scale (POSAS)

The POSAS was used as an objective assessment tool to analyze satisfaction regarding scarring. It consists of two numeric scales: the Observer Scar Assessment Scale (OSAS) and the Patient Scar Assessment Scale (PSAS). The OSAS includes six domains (vascularity, pigmentation, thickness, relief, pliability, and surface area), each of which is graded numerically on a 10-point scale ranging from 1 (normal skin) to 10 (the worst scar result). The PSAS includes pain, pruritus, color, thickness, surface roughness, and pliability, which are also graded using the 10-point scale. The combination of the patient and observer parts of the scale allows a more complete evaluation.

We used Wilcoxon’s signed rank test to compare the preoperative and postoperative POSAS scores, and p values less than 0.05 were considered statistically significant. Statistical results were calculated using IBM SPSS software, version 23.0 (IBM Corp., Armonk, NY, USA).

3. Results

In total, 15 patients, including 10 males and 5 females with a mean age of 28.53 years (range 16 to 42 years), were reevaluated 12 months after one procedural session (Table 1). The affected bald area was 16.71 cm² (range 1.20 to 130.00 cm²). An average of 584.93 FUs (range 42 to 4,550 FUs) were transplanted with an aesthetically acceptable scar-camouflaging effect, and the mean survival rate was 80.67% (range 70 to 90%). All 15 patients underwent only one procedure session, and the duration of surgery was an average of 1.80 hours (range 0.5 to 5.5 hours). The donor area showed negligible scarring in all cases. No significant complications, such as necrosis, infection, hematoma, or numbness, were observed among the 15 patients.

As shown in Table 2, remarkable improvement was observed after the procedure in terms of patient and observer satisfaction. The PSAS decreased from 13.47 (range 9 to 20) to 6.60 (range 4 to 10), and the OSAS decreased from 11.00 (range 7 to 18) to 5.00 (range 3 to 8) after the procedure. The total postoperative POSAS showed a significant decrease, with a preoperative score of 24.47 (range 16 to 38) and a postoperative score of 11.60 (range 7 to 18), according to Wilcoxon’s signed rank test (p=0.001).

3.1. Case 1

A 19-year-old female patient had undergone surgical fat grafting to the forehead with postsurgical sequela of a necrotic hairless lesion, approximately 130 cm² in area, with a triangular shape, that had remained for longer than a year in the right frontotemporal region of her scalp (Figure 1). In total, 4,550 FUs were harvested from the occipital scalp by the strip excision method and transplanted at a density of approximately 35 FUs/cm². The patient underwent a single surgical session that lasted 5.5 hours. At the twelve-month follow-up, the graft survival rate was 75%. The preoperative POSAS was 20 for the patient scale and 18 for the observer scale; the postoperative scores were 8 and 7 for the patient and observer scales, respectively.

3.2. Case 2

A 42-year-old female patient had a forehead lift using Endotine fixation (Endotine™ forehead bioabsorbable implant, MicroAire Aesthetics, Charlottesville, VA, USA) two years previously, which led to skin necrosis on her left frontotemporal scalp (Figure 2). The affected area was round and 2 x 3 cm² in area, and 210 FUs harvested from the occipital scalp by the FUE method were transplanted into the lesion at a density of 35 FUs/cm². The operation lasted 1.3 hours, and only a single session was required. The graft survival at the 12-month follow-up was 80%. The preoperative POSAS of the patient scale was 12 and that of the observer scale was 9; the postoperative POSAS was of the patient scale was 5 and that of the observer scale was 3.

3.3. Case 3

A 33-year-old female had an approximately 7 x 1 cm² lesion consisting of a postsurgical linear scar on her frontal scalp due to forehead implant insertion three years earlier (Figure 3). In total, 245 FUs were harvested from the occipital scalp using the FUE method and transplanted into the lesion. The operation time was 1.5 hours, and the transplantation was performed at a density of 35 FUs/cm². She underwent only one procedural session and achieved an 85% survival rate at the 12-month follow-up. The preoperative POSAS scores were 14 for the patient scale and 13 for the observer scale; the postoperative POSAS scores were 6 for the patient scale and 4 for the observer scale.

3.4. Case 4

A 28-year-old male patient with a wide forehead had undergone a forehead reduction surgery one year previously, which resulted in a postsurgical linear hairless scar approximately 20 x 1 cm² in area near his hairline (Figure 4). A total of 700 FUs were harvested from the occipital scalp by the FUE method and transplanted into the lesion at a density of 35 FUs/cm². The operation lasted 2.5 hours, and a single session was required. At his 12-month follow-up visit, the graft survival rate was approximately 80%, and the POSAS had decreased from 10 on the patient scale and 8 on the observer scale preoperatively to 6 and 4, respectively, at the postoperative evaluation. Instead of performing forehead reduction surgery, which results in an incision line scar as a secondary complication, hair transplantation can be used as a primary treatment for camouflaging a wide forehead.

4. Discussion

Cicatricial alopecia encompasses a diverse spectrum of disorders characterized by permanent destruction of hair follicles and replacement by fibrous tracts. Unger et al. defined two categories of cicatricial alopecia: stable and unstable. Unstable cicatricial alopecia is the consequence of progressive dermatologic disorders that can recur intermittently over time, such as lichen planopilaris and discoid lupus erythematosus. In contrast, SCAs occur secondary to traumatic events, such as prior surgeries, burns, radiation, and traction injuries, that can cause permanent scarring in hair-bearing regions [1, 23, 24].

Our study focused on surgically induced SCA. The traditional surgical treatment methods for such lesions include excision, local flap, and tissue expansion, which can result in additional scarring, an unfavorable hair growth direction, and vascular network compromises [1, 5]. Some reports have described successful cases of camouflaging postsurgical scar alopecia with hair transplantation [14, 25].

Since the first hair transplantation was introduced by a Japanese dermatologist, Sasagawa, in 1930, hair transplantation techniques have developed further [26]. In 2002, the FUE technique was introduced by Rassman and Bernstein as an alternative method for harvesting scalp strips from the occipital area with the advantage of no need for sutures and no linear scar. However, this method can still cause problems, such as a wider donor area, spot scars, and transection of follicles if performed by an unskilled surgeon. Therefore, care should be taken to reduce these side effects.

The concept of implanting hair follicles has not been widely accepted as a primary treatment for postsurgically occurring alopecia with the presumption that the graft survival rate would be low due to limited vascularity, tissue stiffness, skin thinning, and possible infection at the recipient site [27, 28]. Conversely, some previous studies have shown that, because of the small size and low metabolic requirement of FUs, hair grafts can grow well in scar tissue [13, 25, 29]. According to Shao, hair transplantation in 37 cicatricial alopecia patients with traumatic scars resulted in a 78% survival rate at an average of 13 months of follow-up [14]. Additionally, Jung showed that, among 18 patients who underwent hair follicle transplantation onto posttraumatic scar tissue, 15 showed more than 75% graft survival at the 6-month follow-up visit [5].

In our clinical study, the survival rate of FU transplants ranged from 70 to 90%, with an average of 80.67%. In our clinical study, the survival rate of the FU transplantations ranged from 70 to 90% with an average of 80.67%. This rate is lower than the average survival rate of 90% in normal scalps from our previous experience and previous studies [25, 30–32]. Furthermore, in some cases, the survival rates remained as low as 70%, which is much lower than the average in normal scalps. However, the average survival of 80% is still meaningful because this rate is much higher than our expectation, and the postoperative outcomes were aesthetically pleasing to both the patients and observers.

The overall patient satisfaction was also very high not only because the transplantation results were anesthetically pleasing but also because no potential existed for the development of flap ischemia or exposure of tissue expanders, which could have occurred with traditional surgical methods, such as scar excision, tissue expansion, and local flaps. Additionally, there was no need for general anesthesia or admission care because the procedure lasted only 1.80 hours on average and did not require any specific postoperative care. All patients were treated at an out-patient clinic with minimal recovery time. There was no need for any dressing of small grafts. Only immediate compression for less than 30 minutes was performed at the recipient and donor sites. The patients were able to wash their hair one day after the procedure and to continue with their daily lives.

The approximate density of hair transplantation in this study was 35 FUs/cm², which was determined by the practitioner’s previous experiences. Although debates are ongoing, it is widely accepted that the transplantation of more than 35 FUs/cm² onto normal tissue can induce poor graft growth and even skin necrosis depending on the vascularity of the recipient site [20–22]. In scar tissues, the vascular supply that supports the newly transplanted grafts must be considered carefully in the preoperative evaluation. Additionally, in this study, the transplantation procedure was performed at least 6 months after the operations that induced the postsurgical scar lesions in the original locations. Hair transplantation at a density of 35 FUs/cm² more than 6 months after the original operation resulted in a relatively successful survival rate with no complications, such as skin necrosis, infection, hematoma, and numbness. It is presumable that, after 6 months of recovery, scar tissue on the scalp can supply blood for FU transplantation at an almost similar density as normal scalp tissue.

When grafting onto very thin attenuated skin, grafts should be placed at an acute angle because the tissue bed is very shallow. The use of tumescence before hair transplantation could facilitate the proper placement and optimal growth of grafts in compromised tissues [25]. In this study, Abbasi solution was used to achieve temporary thickness to facilitate easier dissection and implantation, better hemostasis, and adequate anesthesia. Moreover, triamcinolone was added to help minimize postoperative edema and pain.

This study was conducted with only 15 patients over a period of less than 3 years. Further studies should be conducted in the future with additional patients with various affected areas and different types of postsurgical cicatricial alopecia and over longer periods. Specifically, the difference in the histological background of the underlying infrastructure found in the dermis and along the hair follicular unit between the normal scalps and postsurgical scalps with scars should be identified to explain the different hair graft survival rates. Additionally, the average graft survival rate in this study was 80.67%, which was higher than that previously expected for hair transplantation in cicatricial alopecia but still lower than the average survival rate for normal tissues. Various approaches, such as preoperative fat grafts and adipose stem cell grafts, could be combined in advance with hair transplantation to increase the quality and pliability of scar tissue and ultimately increase the graft survival rate [33–35].

5. Conclusions

Treatment of even small hairless lesions is important because it can affect the patient’s psychosocial status. However, hair transplantation for postsurgical SCA is considered challenging because of tissue stiffness and poor blood circulation. FU hair transplantation could be an effective method with several advantages, including relative safety, a high transplantation survival rate, and satisfactory postoperative results, even after a single session.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

Ethical Approval

This study was approved by the Institutional Review Board of the Seoul National University Boramae Medical Center (IRB No. 10-2018-6) as retrospective patient chart review.

Disclosure

None of the authors has a financial interest in any of the products, devices, or drugs mentioned in this manuscript.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

References

W. Unger, R. Unger, and C. Wesley, “The surgical treatment of cicatricial alopecia,” Dermatologic Therapy, vol. 21, no. 4, pp. 295–311, 2008.
View at: Publisher Site | Google Scholar
M. W. G. Lucas, “Partial retransplantation: a new approach in hair transplantation,” The Journal of Dermatologic Surgery and Oncology, vol. 20, no. 8, pp. 511–514, 1994.
View at: Publisher Site | Google Scholar
J. E. Vogel, “Correction of the cornrow hair transplant and other common problems in surgical hair restoration,” Plastic and Reconstructive Surgery, vol. 105, no. 4, pp. 1528–1536, 2000.
View at: Publisher Site | Google Scholar
A. Barrera, “The use of micrografts and minigrafts for the correction of the postrhytidectomy lost sideburn,” Plastic and Reconstructive Surgery, vol. 102, no. 6, pp. 2237–2240, 1998.
View at: Publisher Site | Google Scholar
S. Jung, S. J. Oh, and S. H. Koh, “Hair follicle transplantation on scar tissue,” The Journal of Craniofacial Surgery, vol. 24, no. 4, pp. 1239–1241, 2013.
View at: Publisher Site | Google Scholar
A. R. Diani, M. J. Mulholland, K. L. Shull et al., “Hair growth effects of oral administration of finasteride, a steroid 5 alpha-reductase inhibitor, alone and in combination with topical minoxidil in the balding stumptail macaque,” The Journal of Clinical Endocrinology and Metabolism, vol. 74, pp. 345–350, 1992.
View at: Google Scholar
L. Drake, M. Hordinsky, V. Fiedler et al., “The effects of finasteride on scalp skin and serum androgen levels in men with androgenetic alopecia,” Journal of the American Academy of Dermatology, vol. 41, no. 4, pp. 550–554, 1999.
View at: Publisher Site | Google Scholar
A. L. Dallob, N. S. Sadick, W. Unger et al., “The effect of finasteride, a 5 alpha-reductase inhibitor, on scalp skin testosterone and dihydrotestosterone concentrations in patients with male pattern baldness,” The Journal of Clinical Endocrinology and Metabolism, vol. 79, pp. 703–706, 1994.
View at: Google Scholar
W. D. Leighton, M. L. Johnson, and J. A. Friedland, “Use of the temporary soft-tissue expander in posttraumatic alopecia,” Plastic and Reconstructive Surgery, vol. 77, no. 5, pp. 737–743, 1986.
View at: Publisher Site | Google Scholar
D. A. Hudson and A. O. Grobbelaar, “The use of tissue expansion in children with burns of the head and neck,” Burns, vol. 21, no. 3, pp. 209–211, 1995.
View at: Publisher Site | Google Scholar
F. Giraldo, C. González, I. Garnica, M. Ferrón, and J. A. Rus, “Sideburn reconstruction with an expanded supraauricular trapezoidal flap,” Plastic and Reconstructive Surgery, vol. 100, no. 1, pp. 257–261, 1997.
View at: Publisher Site | Google Scholar
J. E. Leedy, J. E. Janis, and R. J. Rohrich, “Reconstruction of acquired scalp defects: an algorithmic approach,” Plastic and Reconstructive Surgery, vol. 116, no. 4, pp. 54e–72e, 2005.
View at: Publisher Site | Google Scholar
A. Barrera, “The use of micrografts and minigrafts in the aesthetic reconstruction of the face and scalp,” Plastic and Reconstructive Surgery, vol. 112, no. 3, pp. 883–890, 2003.
View at: Publisher Site | Google Scholar
H. Shao, H. Hang, J. Yunyun et al., “Follicular unit transplantation for the treatment of secondary cicatricial alopecia,” Plastic Surgery, vol. 22, no. 4, pp. 249–253, 2014.
View at: Publisher Site | Google Scholar
J. Wang and J. Fan, “Cicatricial eyebrow reconstruction with a dense-packing one- to two-hair grafting technique,” Plastic and Reconstructive Surgery, vol. 114, no. 6, pp. 1420–1426, 2004.
View at: Publisher Site | Google Scholar
M. Gandelman, A. L. L. Mota, P. A. Abrahamsohn, and S. F. De Oliveira, “Light and electron microscopic analysis of controlled injury to follicular unit grafts,” Dermatologic Surgery, vol. 26, no. 1, pp. 25–31, 2000.
View at: Publisher Site | Google Scholar
M. L. Reed and B. H. Grayson, “Single-follicular-unit hair transplantation to correct cleft lip moustache alopecia,” The Cleft Palate-Craniofacial Journal, vol. 38, no. 5, pp. 538–540, 2001.
View at: Publisher Site | Google Scholar
C. G. Gho and H. A. M. Neumann, “Improved hair restoration method for burns,” Burns, vol. 37, no. 3, pp. 427–433, 2011.
View at: Publisher Site | Google Scholar
A. Gholamali, P. Sepideh, and E. Susan, “Hair transplantation: preventing post-operative oedema,” Journal of Cutaneous and Aesthetic Surgery, vol. 3, pp. 87–89, 2010.
View at: Google Scholar
W. R. Rassman, R. M. Bernstein, R. McClellan, R. Jones, E. Worton, and H. Uyttendaele, “Follicular unit extraction: Minimally invasive surgery for hair transplantation,” Dermatologic Surgery, vol. 28, no. 8, pp. 720–728, 2002.
View at: Publisher Site | Google Scholar
N. Patwardhan and V. Mysore, “Hair transplantation: standard guidelines of care,” Indian Journal of Dermatology, Venereology and Leprology, vol. 74, pp. 46–53, 2008.
View at: Google Scholar
T. Nakatsui, J. Wong, and D. Groot, “Survival of densely packed follicular unit grafts using the lateral slit technique,” Dermatologic Surgery, vol. 34, no. 8, pp. 1016–1022, 2008.
View at: Publisher Site | Google Scholar
L. Abal-Díaz, X. Soria, and J. M. Casanova-Seuma, “Scarring alopecia,” Actas Dermo-Sifiliográficas, vol. 103, no. 5, pp. 376–387, 2012.
View at: Publisher Site | Google Scholar
L. C. Sperling and S. E. Cowper, “The histopathology of primary cicatricial alopecia,” Seminars in Cutaneous Medicine and Surgery, vol. 25, no. 1, pp. 41–50, 2006.
View at: Publisher Site | Google Scholar
L. Barr and A. Barrera, “Use of hair grafting in scar camouflage,” Facial Plastic Surgery Clinics of North America, vol. 19, no. 3, pp. 559–568, 2011.
View at: Publisher Site | Google Scholar
M. Sasagawa, “Hair transplantation,” The Japanese Journal of Dermatology, vol. 30, article 493, 1930.
View at: Google Scholar
R. M. Bernstein, W. R. Rassman, W. Szaniawski et al., “Follicular transplantation,” International Journal of Surgery, vol. 3, pp. 119–132, 1995.
View at: Google Scholar
R. M. Bernstein and W. R. Rassman, “Follicular transplantation patient evaluation and surgical planning,” Dermatologic Surgery, vol. 23, no. 9, pp. 771–784, 1997.
View at: Publisher Site | Google Scholar
W. Unger and R. Nordstrom, “Hair transplantation under split-thickness skin grafts and very thin skin,” in Hair transplantation, W. Unger, Ed., pp. 312–317, Marcel Dekker, New York, NY, USA, 3rd edition, 1995.
View at: Google Scholar
S. J. Lee, H. J. Lee, S. J. Hwang et al., “Evaluation of survival rate after follicular unit transplantation using the KNU implanter,” Dermatologic Surgery, vol. 27, no. 8, pp. 716–720, 2001.
View at: Publisher Site | Google Scholar
W. M. Parsley and D. Perez-Meza, “Review of factors affecting the growth and survival of follicular grafts,” Journal of Cutaneous and Aesthetic Surgery, vol. 3, pp. 69–75, 2010.
View at: Google Scholar
M. L. Beehner, “A comparison of hair growth between follicular-unit grafts trimmed “skinny” vs. “chubby”,” Dermatologic Surgery, vol. 25, no. 4, pp. 339-340, 1999.
View at: Publisher Site | Google Scholar
O. Akdag, N. Evin, M. Karamese, and Z. Tosun, “Camouflaging cleft lip scar using follicular unit extraction hair transplantation combined with autologous fat grafting,” Plastic and Reconstructive Surgery, vol. 141, no. 1, pp. 148–151, 2018.
View at: Publisher Site | Google Scholar
D. Matsumoto, K. Sato, K. Gonda et al., “Cell-assisted lipotransfer: supportive use of human adipose-derived cells for soft tissue augmentation with lipoinjection,” Tissue Engineering Part A, vol. 12, no. 12, pp. 3375–3382, 2006.
View at: Publisher Site | Google Scholar
S. R. Coleman, “Structural fat grafts: the ideal filler?” Clinics in Plastic Surgery, vol. 28, pp. 111–119, 2001.
View at: Google Scholar

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Copyright © 2019 Hyokyung Yoo 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.

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