Introduction
Endometriosis is a benign, complex, chronic and progressive
gynecologic disorder defined as the presence of viable, estrogen-
dependent endometrial-like gland and stroma associated with
inflammatory response outside the uterine cavity.1 It is estimated that
endometriosis is present in 6 to 10% of reproductive age women 2
and has been reported as high as up to 40% in subfertile women. 3
Despite great effort to elucidate the etiology of endometriosis, its
pathogenesis remains unclear. Different theories had been proposed to
explain the origin of this enigmatic disease, from the initial retrograde
menstruation theory proposed by Sampson in 1927 to coelomic
pluripotential metaplasia, hematogeneous or lymphatic embolization.4
In a recent comprehensive manuscript, Laganà et al., 5 described an
interesting hypothesis in which deregulation of genes could lead to
aberrations and deregulation within the mesoderm which may cause
aberrant implantation of stem cells in addition to alteration in the
peritoneal microenvironment creating the conditions for proliferation
ectopic endometrial cells. There is three main clinically subtype forms
of endometriosis consisting of
i. Superficial endometriotic implants located on the surface of the
pelvic peritoneum and ovaries (peritoneal endometriosis),
ii. Ovarian cysts lined by endometrioid mucosa (endometriomas),
and
iii. Complex solid masses of endometriosis implants mixed with
adipose and fibromuscular tissue infiltrating the rectovaginal
septum (Deep infiltrating endometriosis. DIE).1
Patients affected by endometriosis often present with a variety of
symptoms including dysmenorrhea, dyspareunia, chronic pelvic pain,
presence of a pelvic mass and/or subfertility. Comorbid conditions
frequently present in patients with endometriosis are fibromyalgia,
interstitial cystitis/painful bladder syndrome, irritable bowel
syndrome, migraine headache and temporomandibular disorders. 6
Laparoscopy with tissue pathologic biopsy is well accepted as
the “gold standard” for the diagnosis of endometriosis and is the
therapeutic approach of choice when medical treatment produce
unsatisfactory results. Accuracy of visual diagnosis at the time of
laparoscopy increases with disease severity. 7 However, as supported
by the European Society of Human Reproduction and Embryology
(ESHRE), histologic confirmation with biopsy is recommended
because visual identification is associated with a high false positive
rate.8,9 Moreover, endometriosis implants are usually found in multiple
different location such as the ovaries, fallopian tubes, utero-sacral
ligaments, broad ligaments, round ligaments, culd-de-sac, ovarian
fossa, bladder serosa, ureters and rectovaginal septum. A thorough
inspection of the peritoneal cavity during laparoscopy is mandatory to
identify all possible endometriosis implants.
Although infrequent, extrapelvic endometriosis can also be found in
the upper abdomen, the appendix, bowel, diaphragm, abdominal wall
as well as abdominal scars and umbilicus, pancreas, spleen, pleura and
pericardium, respiratory system, and on brain tissue. 10–12 Superficial
peritoneal endometriosis can be clinically suspected but unfortunately,
cannot be diagnosed by any non-invasive imaging modality. Accurate
laparoscopic identification of superficial endometriosis implants is
poor. Using conventional laparoscopy with white light the positive
predictive value of suspected endometriosis lesions confirmed with
pathology was only 66%.13 Accurate identification and excision of all
endometriosis lesions is associated with better surgical outcomes and
could possible decrease the recurrence of the disease. 14,15 Enhanced
laparoscopic imaging techniques has been used to improve the
detection and diagnostic accuracy of endometriosis implants. In this
review, we evaluate current available enhance laparoscopic imaging
modalities with emphasis in detection of endometriosis implants.
Enhanced imaging techniques in
endometriosis
Laparoscopic identification of superficial endometriosis implants
represents a challenge for the gynecologic surgeon. Endometriosis
lesions may present in a wide spectrum of appearance according to a
MOJ Womens Health. 2018;7(1):14‒17. 14
©2018 Jose et al. This is an open access article distributed under the terms of the Creative Commons Attribution License , which
permits unrestricted use, distribution, and build upon your work non-commercially.
Laparoscopic enhanced imaging modalities for the
identification of endometriosis implants a review of
the current status
Volume 7 Issue 1 - 2018
Carugno Jose, Andrade Fausto, Laganà
Antonio
Minimally Invasive Gynecology/Robotic Unit, University of
Miami, USA
Correspondence: Jose Carugno, MD FACOG, Department of
Obstetrics and Gynecology, University of Miami, Miller School
of Medicine, Miami, USA, T el 9144739587,
Email
[email protected]
Received: October 22, 2017 | Published: January 11, 2018
Abstract
Endometriosis is a benign, complex, chronic and progressive gynecologic disorder
defined as the presence of viable, estrogen-dependent endometrial-like gland and
stroma associated with inflammatory response outside the uterine cavity. Laparoscopy
with tissue pathologic biopsy is well accepted as the “gold standard” for the diagnosis
of endometriosis and constitute the therapeutic approach of choice when medical
treatment produce unsatisfactory results. Accuracy of visual diagnosis at the time of
laparoscopy increases with disease severity. Enhanced laparoscopic imaging techniques
has been used to improve the detection and diagnostic accuracy of endometriosis
implants. In this review, we evaluate current available enhance laparoscopic imaging
modalities with emphasis in detection of endometriosis implants.
Keywords
endometriosis, laparoscopy, robotics, imaging
MOJ W omen’s Health
Research Article
Open Access
Laparoscopic enhanced imaging modalities for the identification of endometriosis implants a review of
the current status
15
Copyright:
©2018 Jose et al.
Citation: Jose C, Fausto A, Antonio L. Laparoscopic enhanced imaging modalities for the identification of endometriosis implants a review of the current
status. MOJ Womens Health. 2018;7(1):14‒17. DOI: 10.15406/mojwh.2018.07.00160
“lifecycle” of the implants. The lesions can be flat or vesicular. They
can have any combination of color typically red, back/brown and
white. Active “red” lesions, large endometriomas, deep infiltrating
nodules, and typical “powder-burn” lesions are easier to identify
than “white” old fibrotic lesions. The endometriotic implants are
hypervascular. The diagnostic accuracy at laparoscopy is also affected
by the experience of the surgeon and the laparoscopic equipment. 16
Because of the difficulty in diagnosing endometriosis based on visual
appearance, there has been great interest in facilitating laparoscopic
recognition of the implants. Surgeons have always depended on white
light to illuminate their surgical field. Under white light, tissue color
varies in a limited shade of colors mostly red, yellow, white and gray
making it difficult to differentiate normal from pathologic tissue.
Enhanced laparoscopic imaging techniques that allow
differentiation of normal from pathologically infiltrated tissue is
been utilized in different surgical specialties especially in surgical
oncology.17,18 Like malignant process, neovascularization is present
in most endometriosis implants and could be used to differentiate
endometriosis lesions from normal peritoneum. Due to the diverse
visual appearance of the endometriosis implants and the low
positive predictive value of performing peritoneal biopsies based on
appearance, there is great interest in improving accuracy of the visual
diagnosis. Enhanced imaging modalities are used to help the surgeon
to identify peritoneal endometriosis lesions.
Fluorescent Laparoscopy techniques:
Autofluorescence imaging (AFI)
Autofluorecence imaging is an advanced technology that exploits
the autofluorent nature of tissue and allows the detection of small
endometriosis superficial lesions. Although the precise mechanism of
autofluorescence of tissue has not been determined, it is accepted that
it can change if the epithelial layer thickens or if the concentration
of chromophores change second to hypervascularization. 19 This
technique relies on blue light excitation and differences in epithelial
thickness and neovascularization. It produces different color tones
that differentiate endometriosis lesions from normal peritoneum. 20,21
Endogenous fluorophores such as tryotophan, collagen, elastin,
Flavin, and co-enzimes of the respiratory chain lead to tissue
differentiated autofluorescence. Demco L. described the use of
blue light at a frequency of 440Hz to facilitate the visualization of
endometriosis implants in 25 patients with suspected endometriosis.
He concluded that the use of blue light facilitates the visualization of
endometriosis lesions and allow detection of endometriosis implants
not visible with the use of white light. 22 Buchweitz et al., 20 reported
a prospective analysis of 83 patients undergoing laparoscopy for
suspected endometriosis under white light and autofluorescence for
the detection of non-pigmented peritoneal endometriotic lesions.
They reported a sensitivity of 65% with the use of white light and 92%
with the aid of autofluorescence (1.42 fold increase) concluding that
the use of white light and autofluorescence is significantly superior
to white light illumination alone for the detection of non-pigmented
endometriotic lesions.
5-aminolevulinic acid induced fluorescence (5-ALA)
The principle of fluorescent imaging is the use of a special
endoscope that releases light at different wavelength which
stimulates a signal released by the biomarker that is captured by the
endoscope and is then mapped digitally onto a screen. Fluorescence
after administration of 5-ALA is a diagnostic tool used in the early
diagnosis of cancerous disorders in urology and pulmonology. 23,24
5-ALA is a administered as an oral prodrug that increases the level
of protoporphyrin IX in epithelial tissue that is then fluorescently
illuminated. When blue light is then applied following 5-ALA
administration, non-pigmented endometriosis lesions are accentuated.
Patients should avoid exposition to direct sunlight for 24hours
after administration due to photosensitization. A common reported
side effect is nausea and vomiting which occur in up to 10% of
the cases. 20 Malik E et al.,+published a series of 37patients with
suspected endometriosis who underwent diagnostic laparoscopy after
the administration of 30mg of 5-ALA/Kg body weight PO the night
before surgery. They reported a sensitivity of fluorescence diagnosis
of 100% with a specificity of 75%. The likelihood ratio for a positive
test indicating endometriosis was 4.
In contrast, the sensitivity of the visual diagnosis of endometriosis
under white illumination is only 69%, with a specificity of 70%. The
likelihood ratio is 2.3. This represent a diagnostic increase of 46%
compared with white light illumination (sensitivity: 48%, specificity:
60%) The authors concluded that the diagnosis of non-pigmented
occult endometriotic implants is feasible and could help the surgeon
to differentiate endometriotic lesions from other peritoneal unspecific
changes. Buchweitz et al., 26 found similar sensitivity of fluorescence
diagnosis with 20mg/Kg body weight, with the added benefit of
reduced cost and decreased incidence of adverse effects. Fluorescence
diagnosis should be considered as an additional diagnostic tool
that complements the conventional use of white light illumination.
However, it has some limitations that should be considered.
Fluorescence diagnosis cannot replace the use of white light because
the depth of penetration of the blue light is too shallow to detect deep
infiltrating endometriosis. Also, the fluorescence fades with increased
duration of the laparoscopy which prevent its use for the entire case.
Narrow Band Imaging T echniques (NBI)
Narrow Band Imaging (NBI) is a modality that uses a narrow
wavelength of light to change the color contrast of the endoscopic
image improving the detection of neovascularization which allows
visualization of endometriotic implants. In NBI only the green and
blue light of the spectrum are excited. Barrueto et al., 27 reported
the sensitivity and specificity for their clinical impression for the
detection of endometriotic peritoneal implants using NBI and white
light and found that using NBI the sensitivity was 84% and specificity
24% compare to using WL with a sensitivity of 71% and specificity
36%. It is important to note the low specificity which can result in
unnecessary resection of healthy peritoneum, increasing the chance of
surgical complications, with potential increase of postoperative pain
and adhesion formation.
Near-infrared (NIR) imaging with Indocyanine green (ICG)
(FireFly®). Near infrared wavelength is often used in endoscopy as
it results in greater depth of penetration. It is used with indygocianine
green (ICG) as a non-specific biomarker. ICG is a water-soluble tracer
dye that binds to plasma proteins with a peak spectral absorption at
800nm. It is administered intravenously (IV), has a half-life of 3 to
4minutes and is cleared by the liver. This is used with the infrared
fluorescence imaging system integrated with the robotic platform.
There are 2 conventional laparoscopy endoscopes available to use this
technology (Pinpoint, Nvadaq, Canada and D-Light, Storz, Germany)
and one for the Da Vinci robotic platform (FireFly Intuitive Surgical,
Laparoscopic enhanced imaging modalities for the identification of endometriosis implants a review of
the current status
16
Copyright:
©2018 Jose et al.
Citation: Jose C, Fausto A, Antonio L. Laparoscopic enhanced imaging modalities for the identification of endometriosis implants a review of the current
status. MOJ Womens Health. 2018;7(1):14‒17. DOI: 10.15406/mojwh.2018.07.00160
Inc, Sunnyvale, CA) The FireFLy® mode on the da-Vinci Si platform
has been available since 2001 and approved by the Food and Drug
Administration (FDA) for imaging use in August 2014. It facilitates
identifying endometriosis lesions using infrared technology to identify
vascular structures surrounded of fibro-vascular tissue.
It requires the injection of 5mg of ICG into the IV . The
endometriotic lesion will fluoresce as a dark green area surrounded
by a lighter area of fibrosis. In 2015, Guan et al., 28 reported that the
use of FireFly® technology and ICG facilitated the identification of
endometriosis allowing to perform single site laparoscopic excision
of endometriosis nodules with complete resolution of symptoms and
excellent cosmetic results. The use of Firefly technology has also
proven helpful for excision of extragenital endometriosis, in particular
for the excision of implants nodules overlying the ureter and rectum.28
These lesions are often subtle and are not visualized with the use of
white light, but when illuminated using Firefly technology, complete
resection of the targeted affected area is possible. Precaution should
be taken with patients with known iodine allergy, hyperthyroidism or
kidney failure are at increased risk of anaphylaxis.
Conclusion
Laparoscopy is the gold standard for diagnosis and treatment of
endometriosis. The current clinical approach of endometriosis favors
visual inspection and tissue pathologic biopsy diagnosis. Advances
is surgical technology specially enhanced imaging techniques show
encouraging results to improve the identification of endometriosis
implants. Further studies are needed to confirm the clinical benefit of
adopting this promising technological modality.
Compliance of ethical standards
This study received no funding.
Conflicts of interest
i. Jose Carugno declare that he has no financial conflicts to disclose.
ii. Fausto Andrade declare that he has no financial conflicts to
disclose.
iii. Antonio Laganà declare that he has no financial conflicts to
disclose.
Ethical approval
This article does not contain any studies with human participants
or animals performed by any of the authors.
Authors contribution
i. J Carugno: Project development and Manuscript writing.
ii. F Andrade: Project development and Manuscript writing.
iii. AS Laganà: Project development and Manuscript writing.
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