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A New Surgical Treatment of Keloid: Keloid


Core Excision
Article in Annals of Plastic Surgery March 2001
DOI: 10.1097/00000637-200102000-00008 Source: PubMed

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A New Surgical Treatment of


Keloid: Keloid Core Excision
Yoonho Lee, MD*
Kyung-Won Minn, MD*
Rong-Min Baek, MD
Jin Joo Hong, MD*

Keloids and hypertrophic scars result from excessive collagen


deposition, the cause of which is not yet known. Unlike hypertrophic scars, keloids frequently persist at the site of injury, often
recur after excision and always overgrow the boundaries of the
original wound. There have been many trials to control keloids,
but most of them have been unsuccessful. The authors propose a
new surgical technique to treat keloids and name it keloid core
extirpation. They excise the inner fibrous core from the keloid and
cover the defect with a keloid rind flap, which is arterialized by the
subcapsular vascular plexus. The authors treated 24 keloids of
the ear, trunk, face, and genitalia with keloid core excision. Four
cases of partial rind flap congestion or necrosis occurred. Those
patients who healed primarily after surgery showed no evidence of
keloid recurrence as long as they were followed. The authors have
found the keloid core extirpation technique to be excellent in
preventing keloid recurrence, with no adjuvant therapy after
surgery.
Lee Y, Minn K, Rong-Min Baek, Hong JJ. A new surgical treatment of
keloid: keloid core excision. Ann Plast Surg 2001;46:135140

From the *Department of Plastic and Reconstructive Surgery, College of


Medicine, Seoul National University; and Inje University Medical Center,
Seoul, Korea.
Received Dec 20, 1999, and in revised form Sep 6, 2000. Accepted for
publication Sep 6, 2000.
Address correspondence and reprint requests to Dr Lee, Department of
Plastic Surgery, Seoul National University Hospital, 28 Yongon-Dong
Chongno-Gu, Seoul, 110-744, Korea.

Keloids and hypertrophic scars are benign fibrous


growths that usually occur after trauma in predisposed individuals. Alibert1 first clearly described
surface overhealing and proposed the word cheloide in 1817 to differentiate keloids from cancerous overgrowths. The term is derived from the
Greek word chele, which means the claw of a
crustacean. Keloids extend beyond the confines
of the original wound and tend to recur after
excision.2
The incidence of keloid formation is difficult to
assess, ranging from 4.5% to 16% in black and
Hispanic populations,3,4 and is higher during
times of physiological hyperactivity of the pitu-

itary, such as puberty and pregnancy.5 Keloids


are seen more commonly between the ages of 10
and 30,6 and tend to run more in families than
hypertrophic scarring.7 Wounds in the presternal
and deltoid regions, wounds that cross skin tension lines, wound closed under tension, and
wounds in thicker skin have a greater tendency to
heal with an abnormal scar. Some locations almost never develop abnormal scars, such as the
genitalia, the eyelid, the palm of the hand, and
the sole of the feet.8
Despite the disfigurement and symptoms like
pain or pruritus from keloids, the literature offers
little consensus about appropriate therapy. Keloids that are resistant to nonsurgical treatment
modalities such as corticosteroid injection, pressure therapy, or silicon gel sheeting should be
considered for surgical excision. According to a
review of the literature, surgical excision alone
leads to recurrence rates that range from 45% to
100%.9
When surgery is combined with intralesional
corticosteroids, the recurrence rate in the majority of studies falls below 50%.9 Surgery combined with button compression therapy on the
earlobe led to no recurrence.10 External surface
radiation after excision, often combined with
other therapies, has been associated with recurrence rates of less than 10%.11 Various lasers
have been used in the treatment of keloids with
great variability in the recurrence rate, but in
general they result in recurrence rates similar to
conventional surgery.12 Interferon--2b injected
after keloid excision demonstrated an 8% recurrence rate in a small series of patients.13 We
developed a new surgical technique to treat keloids, for which adjuvant therapy to prevent
keloid recurrence is unnecessary.
Our treatment consists of excising the fibrous
core of the keloid, which leaves a shell or rind of
the keloid attached to the normal skin as a flap
Copyright 2001 by Lippincott Williams & Wilkins, Inc.

135

Annals of Plastic Surgery

Volume 46 / Number 2 / February 2001

and a rim of scar as a splint. We then resurface


the defect with a keloid rind flap that is well
nourished by the subcapsular vascular plexus.

congestion, the patient is placed in the hyperbaric oxygen chamber at 2.4 atm three times a day
for 3 to 5 days. No adjuvant therapy to prevent
keloid recurrence was necessary after surgery.

Patients and Methods


Results
Patients
Twenty-one Korean patients with 24 keloids resistant to pressure therapy and repeated intralesional steroid injection underwent keloid core
extirpation surgery at Seoul National University
Hospital between June 1987 to October 1995
(Table). The keloids varied in size from 1 1.5 to
5 6 cm.
Patient age ranged from 13 to 40 years (mean
age, 24.9 years). The patient group consisted of
11 women and 10 men. The ear (N 14) was
the most common location of the keloid followed by the trunk (N 4), face (N 4), and
genitalia (N 2). In contrast to the general
belief that the genitals are immune to keloid
reaction, there was a case of keloid of the
labium major after excision of a redundant left
labium majora, and a case of keloid of the
prepuce after circumcision.
Operative Procedure
We prefer to use local anesthesia. An incision is
made approximately halfway around the keloid1
mm within the keloid edge. The keloid rind flap,
which consists of epidermis and thin dermis overlying the keloid, is raised from the fibrous keloid
core. It is mandatory to include the subcapsular
vascular plexus underneath the flap(Fig 1). This
flap is easily separated from the keloid core with
the scalpel, especially when the local anesthetic
agent is administered between the flap and the
keloid core. It is important to keep the base of the
flap as wide as possible to prevent flap congestion.
After raising the flap completely, the fibrous keloid
core is extirpated through the avascular cicatricial
plane, leaving a thin margin of scar tissue in the
normal tissue. After trimming the redundant keloid
rind flap, defects are resurfaced with the flap. All
wounds are closed with one layer of 6-0 black silk
without tension, and a tie-over dressing is applied
to prevent hematoma formation and to release
tension.
If the circulation of the flap shows marked
136

Follow-up ranged from 6 months to 12 years


(mean follow-up, 20 months). Both surgeon and
patient estimated the results (Figs 35). Twelve
patients (62.5%) were highly satisfied with their
result, and were rated as good by the surgeon.
Four patients (17.7%) showed general satisfaction but wanted aesthetic refinement of the results, and those patients were rated as fair by the
surgeon. Two patients (8.3%) showed no evidence of recurrence after surgery, but disliked the
result because of the discoloration and irregularity of the scar surface. These patients were rated
as poor by the surgeon.
Partial recurrence of the keloid occurred in 3
patients (12.5%). Two recurrences occurred after
partial flap necrosis, which occurred postoperatively. One patient with a chin keloid showed
recurrence of the keloid 3 months after surgery
probably because of poor hematoma control. Simple flap congestion did not affect the final result
when managed immediately with hyperbaric oxygen therapy.
Keloids of the ear and genitalia yielded a high
satisfaction rate partly because of their concealed
location. That is, removal of the mass itself was a
relief to most of the patients. Meanwhile, core
extirpation of keloids of the face and trunk produced less aesthetically pleasing reactions, despite the elimination of the keloid. Poor color and
texture match of the flap with surrounding skin
contributed to the poor final score.

Discussion
The etiology of keloids is not yet fully known.
This is due, in part, to the lack of a reliable in
vivo experimental model, because abnormal scar
formation is a unique phenomenon that occurs in
humans. However, a variety of genetic and environmental causes have been implicated in the
pathogenesis of abnormal scars such as keloids

Lee et al: Keloid Core Excision

Patient Characteristics
Age,
Patient Sex yr
Location

Size, cm

Complication/Treatment

Result

JKL
JNL
EHK
KSH
HHL
JSP
HAP
EKO
YSL
DHC
JYK
JDH
YOC
YYA
NSC
WHH
IJK
JDH

M
F
F
F
M
M
F
F
M
M
F
M
F
F
M
M
F
M

22
40
27
38
16
17
19
25
40
19
22
23
16
33
33
13
21
24

Bilat. preauricular
Bilat. earlobes
Presternal
Bilat. earlobes
Lt. upper helical rim
Lt. retroauricle
Rt. earlobe
Lt. shoulder
Rt. retroauricle
Rt. retroauricle
Lt. upper lip
Lt. chin
Lt. scapula
Lt. earlobe
Lt. helical rim
Penile prepuce
Rt. earlobe
Rt. cheek

2.2 1.8/3 1.7


2.4 2.4/2.1 2
4.5 2
3 3/2.3 2.3
4.6 2.6
2.8 2.3
2.1 2.2
1.8 1.8
2.5 1.7
32
1.5 1.2
2 2.1
5 5.8
2.8 2.5
2.1 2.3
1.4 1.6
1.9 1.9
56

G
G
P
G
G
G
F
F
G
G
P
Recurrence
F
G
G
G
G
Partial recurrence

CYL

17

Lower abdomen

SOP
MYC

F
F

35
23

Lt. upper lip


Lt. labium majora

None
None
None
Partial flap congestion/HBO therapy
None
None
None
None
None
None
None
None
Partial flap congestion/HBO therapy
None
None
None
None
Partial flap loss/HBO therapy and
secondary healing
Partial flap loss/HBO therapy and
secondary healing
None
None

36
1 1.5
3.8 2.4

Partial recurrence
F
G

M male; F female; Bilat. bilateral; Rt. right; Lt. left; HBO hyperbarric oxygen; G no recurrence of keloid and good
aesthetic result; F no recurrence of keloid and fair aesthetic result; P no recurrence of keloid with poor aesthetic result.

Fig 1. (A, B) The subcapsular vascular plexus is identified just beneath the fibrous capsule of the keloid.
Hematoxylin eosin stain, original magnification 50 (A) and 100 (B) before 37% reduction.

and hypertrophic scars.14 The result is a tissue


mass with overabundant extracellular matrix.
Glycoproteins and water are both increased notably in the extracellular matrix of keloids and
hypertrophic scars.15 There is also an excessive
accumulation of collagen from increased collagen
synthesis or decreased collagen degradation.16,17
The rate of collagen synthesis in keloids is
markedly elevated, although it usually diminishes after 2 to 3 years.18 21 Although the concen-

tration of collagenase is increased in keloids,


tissue -globulins such as -2 macroglobulin and
alpha-1 antitrypsin inhibit collagenase function
and are found in increased amounts.22,23 Although emerging knowledge has influenced dramatically the way we think of abnormal scar
formation, very little of this basic research has
translated into clinical wound management.
A variety of keloid treatment options has been
proposed and practiced with limited success.
137

Annals of Plastic Surgery

Volume 46 / Number 2 / February 2001

Fig 2. (A) Preoperative keloid at the posterior surface of the auricle. (B) The keloid rind flap has been elevated from
the keloid core. (C) Postoperative result 5 months after core extirpation.

Fig 3. (A) A keloid at the anterior surface of the auricle. (B) Postoperative result 3 years after core extirpation.

The options include surgery, irradiation, pressure, silicon gel sheeting, laser, and pharmacological agents such as corticosteroid, vitamin A,
-amino-propionitrile, asiaticoside, zinc oxide,
138

and tranilast. However, as a single modality,


none of them shows satisfactory results in terms
of cosmetic and symptomatic aspects.
In a large review of the literature, Friedman24

Lee et al: Keloid Core Excision

Fig 4. (A) A keloid of the labium major after trauma. (B) Postoperative result 2 years after core extirpation.

Fig 5. (A) Keloid of the shoulder. (B) Postoperative result 6 months after core extirpation. (C) Postoperative result 12
years after core extirpation. There has been no recurrence.

proposed surgical excision and corticosteroids for


small keloids, pressure therapy plus surgerysteroid combination for moderately large scars, and
combination surgery and postoperative radiotherapy for very large, resistant scars. Although surgical
excision combined with radiotherapy has demonstrated fairly successful results in treating resistant
keloids, many surgeons are still reluctant to use
ionizing radiation in the treatment of benign
disease.
Several modifications in surgical technique have
been proposed to achieve successful closure of the
wound with minimal tension after keloid excision.
However, a skin graft or local flap needs a donor
site and leaves unnecessary scars. On histological
analysis, we determined that the subcapsular vascular plexus offers a rich blood supply to the
capsular rind flap. During the immediate postoperative period, wound tension can be reduced using a
tie-over dressing. Furthermore, because the rind
flap serves as a splint and decreases the transmission of tensile forces to the central area of the
lesion, keloid recurrence was prevented, with no
adjuvant therapy.
The limitation of this technique lies in the size

of the keloid. We experienced two cases of partial


necrosis and two cases of temporary flap congestion, all of which occurred in large keloids. Because, especially in large keloids, the base of the
flap is narrower than the width of the flap, necrosis of the distal end of the flap can be anticipated,
and a cautious design is mandatory. We have
used hyperbaric oxygen therapy for cases of flap
congestion, and have salvaged more than 50% of
the compromised flap.
The rind flap, which is nourished via the subcapsular vascular plexus, survived well enough
to maintain tension-free status to prevent recurrence of keloid. The keloid core extirpation technique, which consists of excising the keloid core
and resurfacing the defect using its own keloid
rind flap, has demonstrated excellent results in
preventing keloid recurrence, without requiring
adjuvant therapy.

References
1

Alibert JLM. Quelques recherches sur la cheloide. Mem


Soc Med Emul 1817;744
139

Annals of Plastic Surgery


2

3
4
5
6
7
8
8
9

10
11

12
13

14

Volume 46 / Number 2 / February 2001

Peacock Jr EE, Madden JW, Trier WC. Biological basis for


the treatment of keloids and hypertrophic scars. South
Med J 1970;63:755760
Cosman B, Crikelair GF, Ju DM, et al. The surgical treatment of keloids. Plast Reconstr Surg 1961;27:335345
Oluwasanmi JO. Keloids in the African. Clin Plast Surg
1974;1:179 195
Koonin AJ. The aetiology of keloids: a review of the literature
and a new hypothesis. South Afr Med J 1964;38:913917
Murray JC, Pollack S, Pinnell SR. Keloids. A review. J Am
Acad Dermatol 1981;4:461 470
OmoDare P. Genetic studies on keloids. J Natl Med Assoc
1975;67:428 432
Crokett DJ. Regional keloid susceptibility. Br J Plast Surg
1964;17:245253
Crokett DJ. Regional keloid susceptibility. Br J Plast Surg
1964;17:245253
Lawrence NT. In search of the optimal treatment of keloids: Report of a series and a review of the literature. Ann
Plast Surg 1991;27:164 178
Brent B. The role of pressure therapy in management of
earlobe keloids. Ann Plast Surg 1978;1:579 581
Ship AG, Weiss PR, Mincer FR, et al. Sternal keloids:
successful treatment employing surgery and adjunctive
radiation. Ann Plast surg 1993;31:481 487
Berman B. Bieley HC, Adjunct therapies to surgical management of keloids. Dermatol Surg 1996;22(2):126 130
Berman B, Duncan MR. Short-term keloid treatment in
vivo and human interferon alpha-26 results in selective
and persistent normalization of keloidal fibroblast collagen, glycosaminoglycan and collagenase production in
vitro. J Am Acad Dermatol 1989;21:694 702
Thomas DW, Hopkinson I, Harding KG, Shepherd JP. The

140

15

16

17

18

19

20

21

22
23

24

pathogenesis of hypertrophic keloid scarring. Int J Oral


Maxillofac Surg 1994;23:232236
Kischer CW, Shetlar MR. Collagen and mucopolysaccharides in the hypertrophic scar. Connect Tissue Res 1974;
2:205213
Cohen IK, Diegelmann RF. The biology of keloid and
hypertrophic scar and influence of corticosteroids. Clin
Plast Surg 1977;4:297299
Cohen IK, Keiser HR, Sjoerdsma A. Collagen synthesis in
human keloid and hypertrophic scars. Surg Forum 1971;
22:488 489
Diegelmann RF, Cohen IK, McCoy BJ. Growth kinetics and
collagen synthesis of normal skin, normal scar, and keloid
fibroblasts in vitro. J Cell Physiol 1979;98:341346
Craig RDP, Schofield JD, Jackson DS. Collagen biosynthesis in normal and hypertrophic scars and keloids as a
function of duration of the scar. Br R Surg 1975;62:741
744
Craig RDP, Schofield JD, Jackson SS. Collagen biosynthesis in normal human skin, normal and hypertrophic scar
and keloid. Eur J Clin Invest 1975;5:69 74
McCoy BJ, Galdun J, Cohen IK. Effects of density and
cellular aging on collagen synthesis and growth kinetics in
keloid and normal skin fibroblasts. In Vitro 1982;18:
79 86
McCoy BJ, Cohen IK. Collagenase in keloid biopsies and
fibroblasts. Connect Tissue Res 1982;9:181185
Diegelman RF, Bryant CP, Cohen IK. Tissue alphaglobulins in keloid formation. Plast Reconstr Surg 1977;59:418
423
Friedman RM. Abnormal scars. Sel Read Plast Surg 1995;
8:20 27

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