|
2002 Selected Articles
Vaginal Reconstruction
Ramin Mirhashemi, MD; Nicholas Lambrou, MD
Vaginal reconstruction has its origin in antiquity with the
first known description of a surgical repair of a "membranous
obstruction" of the vagina attributed to Hippocrates.1 Several
hundred years later, in the first century AD, the great Roman
medical writer Celsus detailed a surgical approach to correct
imperforate hymen and vaginal atresia. Although several other
commentaries on the surgical treatment of vaginal atresia were
documented in the ensuing years, it was not until the latter
half of the 19th century that operations of a truly plastic and
reconstructive nature were performed. These included the use
of local flaps from the labia, as well as skin grafts. The aim
of the current discussion is to summarize various techniques
of vaginal reconstruction and focus on the recent advances in
such repairs after radical resection for pelvic malignancies.
Vaginal reconstruction has been expanded to include women who
have undergone surgical removal of the vagina, most commonly
as part of pelvic exenteration for malignancies of the cervix,
vagina, or vulva. Pelvic exenteration is one of the most extensive
and potentially most morbid procedures performed in gynecologic
oncology (Figures 1 and 2), but it can be curative in up to 50%
of properly selected patients.2,3 Over the past two
decades, reconstruction has played an increasingly important
role in preserving both function and cosmetic appearance. Of
these, continent urinary diversions such as the Miami pouch (Figure
3) and colorectal reanastomosis (Figure 4) have gained acceptance
as successful, low-morbidity procedures that decrease the need
for external appliances. The most recent advances have been in
reconstructions of the vagina.
Figure 1.
|
Figure 2.

|
Figure 3.
|
Figure 4.

|
Currently, several options are available for reconstructing
the vagina and vulva. These include the use of skin grafts (either
partial or full thickness), various intestinal substitutes, local
flaps, thigh flaps, and abdominal myocutaneous flaps. Each of
these methods has its benefits and potential risks. Vertical
and transverse rectus abdominis myocutaneous (RAM) flaps are
the current frontrunners in popularity.
There are several goals for vaginal reconstruction in patients
with malignancies. The first is to restore the anatomy of the
surgically created defect without compromising curability of
disease. The second is to improve the patient's quality of life
by rebuilding a functional vagina. Data indicate that these two
goals are intimately related. The largest predictor of patient
satisfaction after any type of vaginal reconstruction is control
of pelvic disease.4 Other important considerations
are to minimize intraoperative time and to improve both intra-
and postoperative short- and long-term morbidity.
SKIN GRAFTS
McIndoe is credited with popularizing the use of a split-thickness
skin graft in creating a neovagina.5 In this type
of reconstruction, skin grafts from 0.016 to 0.020 inches in
thickness are obtained from the thigh or buttock and sutured
or glued over a prosthetic vaginal stent.6 A space
is surgically created between the bladder and rectum, and the
stent with the overlying skin graft is then sutured into place.
Various stenting materials may be used, including glass dilators,
tightly packed gauze, foam in sterile condoms, and partially
inflated tissue expanders. The fitting of the stent and proper
preparation of the graft are more important than the actual stent
type.7,8 The stent is typically removed 7 days postoperatively,
and the patient is discharged with instructions to wear a stent
or prosthesis for up to 6 months.9 Success rates of
85% to 89% have been reported, with up to 94% patient approval
(defined as regular intercourse with satisfaction and adequate
vaginal capacity).2,4
Disadvantages of grafting include contracture, which occurs
in up to 42% of patients (compliance with daily stent use in
the first 6 months may help to prevent this).2 Patients
also need to use lubricants during intercourse, and the vaginal
configuration is less anatomic. Benefits include low morbidity
and mortality, a good cosmetic result with skin graft donor sites
from the buttock or thigh, and (because of the vaginal approach)
no need for laparotomy. Anatomically, this procedure requires
the presence of the bladder and rectum, and may therefore be
more applicable to patients with congenital absence of the vagina
than to those undergoing exenteration for malignancy.
Full-thickness skin grafts are less likely to contract, and
do not require prolonged stenting. Foam rubber in a condom may
be worn for the first month while the graft is maturing, and
thereafter only at night for the next 3 months.10 Donor
sites include hairless inguinal or gluteal regions that can be
closed primarily. In cases where malignancy involves the lower
third of the vagina or vulva, these sites should be avoided secondary
to the potential for lymphatic metastasis of disease.
When available, the omentum has been employed to protect the
pelvis after exenteration. A modification of this includes the
use of a split-thickness skin graft in the creation of a neovagina.
First described by Wheeless,11 a series of 20 patients
undergoing pelvic exenteration was then reported by Kusiak et
al12 in which an omental "J" flap was used with a
split-thickness skin graft. The vascular supply from the left
gastroepiploic artery is preserved, and the omental flap is draped
into the pelvis along the left paracolic gutter. A split-thickness
skin graft (0.018 inches thick) is placed on an adjustable vaginal
stent with the dermis facing outward, and this is inserted into
the pelvis and the omentum is wrapped into a cylinder around
it. Kusiak et al12 reported graft viability in all
patients and functional potential (ie, the capability of intercourse)
in 80%. Vaginal stents must be worn postoperatively for 4-8 weeks,
and results are dependent on an adequate omentum.
INTESTINAL SUBSTITUTES
Intestinal substitutes have been used since the early 1900s
with the introduction of ileal segments for vaginal reconstruction.
However, the small bowel mucosa does not tolerate trauma well,
and may bleed during intercourse. In 1955, Alexadrov13 published
his series of 175 patients undergoing sigmoid neovaginal reconstruction,
reporting a success rate of 89%. Sigmoid neovaginal reconstruction
has been described using a loop technique14 or an
isolated segment15 of sigmoid colon (Figure 5). The benefits
of the sigmoid neovagina include no need for postoperative stenting
and a large lumen with little tendency for stenosis. Dilators
are sometimes required (especially in the pediatric population),
and prolapse of the distal segment can occur, requiring surgical
repair.16 Major disadvantages are voluminous secretions
and an unpleasant odor that can be ameliorated with daily vaginal
douching.
Figure 5.
|
More recently, Filipas et al17 have reported on their
series of 17 patients undergoing vaginal reconstruction with
a segment of cecum and ascending colon. The most common indication
for vaginal reconstruction in this series was congenital anomaly.
Four of the patients had previously undergone vaginal reconstruction.
The operative technique incorporates a 15-cm segment of cecum
and ascending colon, with preservation of the ileocolic artery.
The proximal end is closed, the segment rotated into the pelvis,
and the distal end anastomosed to the vulva. The majority of
patients in this series (13 of 14) reported minimal to no secretions
and overall satisfaction with the vaginal reconstruction, both
sexually and cosmetically (12 of 14). In three patients, a continent
urinary diversion was also created with the use of either transverse
colon or rectosigmoid. This alternative technique for vaginal
reconstruction may prove advantageous in selected patients, but
it would have limited utility in centers where continent urinary
diversions incorporate the cecum and ascending colon.18,19 In
addition, a majority of the patients had gastrointestinal complications
postoperatively, most likely related to the multiple gastrointestinal
anastomoses and diversion of large segments of bowel for both
the neovagina and urinary diversion.
FLAP TECHNIQUES
Local Flaps
Vulvoperineal fasciocutaneous flaps have been used for reconstruction
of the vagina, most often in cases of vaginal agenesis. The paired
flaps are based on the terminal vessels of the internal pudendal
artery. These are small flaps, and are not recommended for irradiated
or extensive defects. Other local flaps include the perineal
artery fasciocutaneous flap20 and labial flaps, but
these are fragile and subject to necrosis without offering much
benefit for either filling the pelvic defect or restoring sexual
function.
Gracilis Flaps
Gracilis myocutaneous flaps have been used in reconstruction
of the vagina since the first publication in 1976 by McCraw et
al.21 The flap derives its blood supply from the medial
femoral circumflex artery, and flap viability has been consistently
reported at 80% to 90%.22,23 Advantages of this technique
include the ability to fill a large pelvic defect with well-vascularized
tissue, and multiple series have reported decreased postoperative
morbidity in patients undergoing pelvic exenteration with reconstruction.
Disadvantages of this flap include the bilateral scars on the
inner thighs from the donor sites and a propensity to prolapse
(Figure 6). Modifications have included the use of shorter flaps
and attachment to levator, presacral, or retropubic fascia.
Figure 6.
|
Rectus Abdominis Flaps
Since the adoption of the gracilis myocutaneous flap with its
notable improvements over skin grafts and local flaps by providing
a bulk of healthy tissue, attention was turned to other sources
for myocutaneous flaps. Tobin and Day24 were among
the first to report on their success with the use of the RAM
flap in vaginal reconstruction. The RAM flaps can be used for
reconstruction of the vulva or vagina, as well as for pelvic
and lower abdominal-wall defects. These flaps are based caudally
on the deep inferior epigastric vascular pedicle to the rectus
abdominis muscle, and carry a myocutaneous paddle from the upper
abdomen (Figures 7 through 9). The skin paddle can be oriented
vertically, obliquely, or horizontally to fit the size and shape
of the defect. There are several anatomic advantages of the distally
based RAM flaps. The entire rectus abdominis muscle may be used,
allowing for a long arc of rotation deep into the pelvis without
compromising the vascular pedicle. The muscle provides a bulk
of healthy tissue to fill the empty pelvic cavity. The fascial
donor defect is located above the linea semicircularis, thus
minimizing the potential for hernia formation; the posterior
rectus sheath remains intact. The skin donor site is located
in the upper abdomen, away from the colostomy and urinary conduit
stomas. Cosmetically, the RAM neovagina yields excellent results,
and the majority of patients appear to be satisfied with both
the cosmetic and functional outcome.
Figure 7.
|
Figure 8.
|
Figure 9.
 |
Data seem to support several advantages of the RAM neovagina
over other types of vaginal reconstruction in patients who have
undergone pelvic exenteration. This may be particularly true
in patients with previous pelvic irradiation. Graft viability
is 82% to 91% in the largest reported series.2,25,26 Smith
et al2 identified potential risk factors for graft
compromise (either partial or complete graft loss), including
preexisting stomas on the same side as the donor site, previous
abdominal incision, and prolonged operative time. Factors such
as obesity, smoking, and peripheral vascular disease may reduce
graft viability, so appropriate patient selection is important.
The majority of patients undergoing exenteration have had previous
pelvic irradiation. The incidence of fistula formation in this
population is 16% when no pelvic reconstruction is performed,
and may carry mortality of up to 40%, especially in the immediate
postoperative period.3,27 Miller et al16 reported
on the benefits of routinely using either an omental pedicle
graft or a gracilis myocutaneous flap in pelvic reconstruction,
and demonstrated a reduction in the incidence of fistula formation
from 16% to less than 5%. One of the largest predictors of fistula
formation in that group was pelvic infection.16 The
use of RAM vaginal reconstruction appears to decrease the risk
of fistula formation as well.4 The deep inferior epigastric
artery originates from the external iliac artery and is generally
spared the damaging effects of pelvic irradiation. This offers
a reliable blood supply to the rectus abdominis muscle from the
symphysis to the costal arch,28 and provides a bulk
of healthy tissue for the evacuated pelvis.
Jurado et al17 reported their results from a series
of 16 patients who underwent vaginal reconstruction with an RAM
flap (68.8%), gracilis flap (12.5%) or Singapore fasciocutaneous
flap (12.5%). They demonstrated a reduction in the incidence
of postoperative pelvic abscess from 27% (6/29) in patients who
had no vaginal reconstruction compared with no pelvic abscesses
in the group who underwent vaginal reconstruction. There were
no significant differences between the neovagina and nonneovagina
groups with respect to other postoperative morbidities.
Fascial dehiscence is an unusual but potentially life-threatening
complication of pelvic exenteration. The donor site of RAM flaps
generally includes a paddle of skin, subcutaneous tissue, anterior
rectus fascia, and underlying rectus muscle with dimensions of
approximately 12 x 20 cm. The donor site is taken from above
the linea semicircularis in a vertical flap, and therefore the
posterior rectus sheath remains intact. If the anterior rectus
sheath is closed, mesh may occasionally be required, or a modification
employed involving a narrower donor site that permits easier
fascial closure.4 Alternatively, a horizontal donor
site can be obtained from below the umbilicus to allow for anatomic
closure of the anterior rectus sheath.
POSTRECONSTRUCTION SEXUAL FUNCTION
Data concerning sexual function after vaginal reconstruction
are limited. In the report by Smith et al,4 nearly
85% of cancer survivors who underwent vaginal reconstruction
with RAM flaps reported sexual satisfaction after the procedure—an
improvement over the 47.5% of patients who reported sexual satisfaction
after vaginal reconstruction with gracilis myocutaneous flaps.29 The
majority of published reports on sexual function after vaginal
reconstruction are confounded by an absence of formal preoperative
sexual assessment and by small numbers of patients. More attention
must be directed toward prospective analysis of sexual function
after vaginal reconstruction.
CONCLUSION
Recent advances in radiation and chemotherapy have improved
response rates and survival in women with gynecologic malignancies.
Nonetheless, radical resection of pelvic tumors remains a crucial
part of the gynecologic oncologist's armamentarium. In the properly
selected patient, pelvic exenteration may be the only real hope
for women who have not responded to more conservative treatments.
The past 30 years have demonstrated improvements in patient selection,
perioperative supervision in the intensive care unit setting,
and surgical reconstructive techniques. Just as the creation
of continent urinary diversions is becoming a standard practice
among qualified gynecologic surgeons when removing the bladder
for gynecologic malignancy (eliminating the need for an external
urinary appliance) so too may vaginal reconstruction become the
option of choice in properly selected patients. The challenge
for the surgeon is to successfully remove the invading cancer
so as not to compromise cure, and to select a reconstructive
technique that reduces postoperative morbidity and provides lasting
sexual function. Recent advances in the use of myocutaneous flaps
appear to offer promise in this arena.
Efforts continue to meet the needs of women faced with this
emotionally and physically devastating threat to their well-being.
For the general internist or OB/GYN, a sensitivity to these needs
and an understanding of vaginal reconstruction are essential
to ensure that patients know about the alternatives available
to them. This includes annual vaginal examinations and cytology,
as the risk of recurrence or a second skin-related primary malignancy
must not be overlooked. In addition, the periodic use of vaginal
dilators, lubricants, and local estrogen supplements may be indicated.
Ramin Mirhashemi, MD, is associate professor,
division of gynecologic oncology at the University of Miami College
of Medicine, Fla. Nicholas Lambrou, MD, is senior
gynecologic oncology fellow, University of Miami School of Medicine,
Fla.
References
- Goldwin RM. History of attempts to
form a vagina. Plast Reconstr Surg. 1997;3:319-329.
- Rutledge FN, Smith JP, Wharton JT,
et al. Pelvic exenteration: analysis of 296 patients. Am
J Obstet Gynecol. 1977;129: 881-892.
- Averette HE, Lichtinger M, Sevin BU,
et al. Pelvic exenteration: a 15-year experience in a general
metropolitan hospital. Am J Obstet Gynecol. 1984;150:179-182.
- Smith HO, Genesen MC, Runowicz CD,
et al. The rectus abdominis myocutaneous flap: modifications,
complications, and sexual function. Cancer. 1998;83:510-520.
- McIndoe A. The treatment of congenital
absence and obliterative conditions of the vagina. Br
J Plast Surg. 1950;2:254.
- Ceuppens H. Application of the fibrin
adhesion system in vaginal reconstruction [letter]. Plast
Reconstr Surg. 1988;81: 815-816.
- Beemer W, Hopkins MP, Morley GW. Vaginal
reconstruction in gynecologic oncology. Obstet Gynecol.
1988;72:911-914.
- Martello JY, Vasconez HC. Vulvar and
vaginal reconstruction after surgical treatment for gynecologic
cancer. Clin Plast Surg. 1995;22:129-139.
- Song IC, Cramer MS, Bromberg BE. Primary
vaginal reconstruction after pelvic exenteration. Plast
Reconstr Surg. 1973;51:509-513.
- Sadove RC, Horton CE. Utilizing full-thickness
skin grafts for vaginal reconstruction. Clin Plast Surg.
1988; 15:443-448.
- Wheeless CR Jr. Neovagina constructed
from an omental J flap and a split thickness skin graft. Gynecol
Oncol. 1989;35:224-226.
- Kusiak JF, Rosenblum NG. Neovaginal
reconstruction after exenteration using an omental flap and
split-thickness skin graft. Plast Reconstr Surg.
1996;97:775-783.
- Alexandrov MS. Obrazovanie Iskustvennogo
Vlagalishcha iz Sigmovidnoi Kishki. Moskva, Medgiz.
1955:185
- Pratt JH, Smith GR. Vaginal reconstruction
with a sigmoid loop. Am J Obstet Gynecol. 1966;96:31-34.
- Shiromizu K, Ogawa M, Kotake K, et
al. Reconstruction of sigmoid vagina and conduit in total
pelvic exenteration for recurrent cervical carcinoma. Jpn
J Clin Oncol. 1989; 19:170-172.
- Hendren WH, Atala A. Use of bowel for
vaginal reconstruction. J Urol. 1994;152 (2 pt 2):752-755.
- Filipas D, Black P, Hohenfellner R.
The use of caecal bowel segment in complicated vaginal reconstruction. BJU
Int. 2000;85:715-719.
- Penalver MA, Benjany DE, Averette HE,
et al. Continent urinary diversion in gynecologic oncology. Gynecol
Oncol. 1989;34:274-288.
- Rowland RG, Mitchell ME, Bihrle R,
et al. Indiana continent urinary reservoir. J Urol.
1987;137:1136-1139.
- Hagerty RC, Vaughn TR, Lutz MH. The
perineal artery axial flap in reconstruction of the vagina. Plast
Reconstr Surg. 1988;82:344-345.
- McCraw JB, Massey FM, Shanklin FD,
et al. Vaginal reconstruction with gracilis myocutaneous
flaps. Plast Reconstr Surg. 1976;58:176-183.
- Berek JS, Hacker NF, Lagasse LD. Vaginal
reconstruction performed simultaneously with pelvic exenteration. Obstet
Gynecol. 1984;63:318-323.
- Copeland LJ, Hancock KC, Gershenson
DM, et al. Gracilis myocutaneous vaginal reconstruction concurrent
with total pelvic exenteration. Am J Obstet Gynecol.
1989;160(5 Pt 1): 1095-1101.
- Tobin GR, Day TG Jr. Vaginal and pelvic
reconstruction with distally based rectus abdominis myocutaneous
flaps. Plast Reconstr Surg. 1988;81:62-73.
- Carlson JW, Soisson AP, Fowler JM,
et al. Rectus abdominis myocutaneous flap for primary vaginal
reconstruction. Gynecol Oncol. 1993;51:323-329.
- Jurado M, Bazan A, Elejabeitia J, et
al. Primary vaginal and pelvic floor reconstruction at the
time of pelvic exenteration: a study of morbidity. Gynecol
Oncol. 2000;77: 293-297.
- Miller B, Morris M, Gershenson DM,
et al. Intestinal fistulae formation following pelvic exenteration:
a review of the University of Texas M.D. Anderson Cancer
Center experience, 1957-1990. Gynecol Oncol. 1995;56:207-210.
- Konerding MA, Gaumann A, Shumsky A,
et al. The vascular anatomy of the inner anterior abdominal
wall with special reference to the transversus and rectus
abdominis musculoperitoneal (TRAMP) composite flap for vaginal
reconstruction. Plast Reconstr Surg. 1997;99:705-710.
- Ratliff CR, Gershenson DM, Morris M,
et al. Sexual adjustment of patients undergoing gracilis
myocutaneous flap vaginal reconstruction in conjunction with
pelvic exenteration. Cancer. 1996;78:2229-2235.
back to top
|