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Evaluation of Intrauterine Pathology: Efficacy of Diagnostic Hysteroscopy in
Comparison to Histopathological Examination
Aisha M Elbareg*, Mohamed O Elmahashi and Fathi M Essadi
Gynecology Department, Misurata Central Hospital/Misurata University, Libyan Arab Jamahiriya, Libya
*Corresponding author: Aisha M Elbareg Gynecology Department, Misurata Central Hospital/Misurata University, Libya, Tel: 00218914213607; E-mail:
elbaregsm@hotmail.com
Received date: April 03, 2015, Accepted date: April 21, 2015, Published date: April 25, 2015
Copyright: © 2015 Elbareg AM, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted
use, distribution, and reproduction in any medium, provided the original author and source are credited.
Abstract
The aim of this work is to evaluate the diagnostic accuracy of hysteroscopy compared to histopathological
findings in cases with intrauterine pathology. This prospective clinical trial was carried out over a period of two years.
280 patients were recruited with an average of 45 years (range: 25-65 years). Two hundred and thirty patients
(82.14%) with abnormal findings in ultrasound examinations, the remaining 50 (17.85%) had normal scan, referred
mainly because of abnormal uterine bleeding (AUB) and infertility. Hysteroscopic findings divided into; uterine cavity
lesions: endometrial or cervical polyps, myomas, cysts, placental derbis, adhesions, congenital malformations and
IUCD retention, endometrial characterization including: functional, dysfunctional, atrophic endometrium, hyperplasia,
polypoid and carcinoma. Biopsies or removal of pathology were performed and sent for histopathology
examinations, results were compared with hysteroscopic findings. Sensitivity, Specificity and predictive value (PV) of
hysteroscopy were calculated. Results: uterine cavity abnormalities were detected in (71.4%) patients, significantly
more at ages of >30 years (58.3%) compared with ages of <30 years (34.6%) (P<0.05). In benign endometrial
lesions, the sensitivity of hysteroscopy was (98.9%), specificity was (97.5%), positive predictive value was (98.8%),
negative predictive value was (98.5%) with diagnostic accuracy of 98.3%, same parameters for endometrial
characterization: (78.9%), (90.7%), (82.8%), (90.9%) with diagnostic accuracy of 87.8%. Conclusions: Hysteroscopy
allows direct visualization of uterine cavity, it is a safe and reliable procedure for evaluating benign endometrial
lesion, but in view of poor validity to exclude endometrial hyperplasia and cancer, it is recommended always to
perform diagnostic hysteroscopy combined with biopsy procedures, giving it an irreplaceable value in diagnosis and
treatment of intrauterine disease.
Keywords: Hysteroscopy; Abnormal uterine bleeding; Infertility;
Endometrial pathology
Introduction
During the last decade hysteroscopy has become the tool of choice
for the evaluation of the endometrial cavity including assessment of
abnormal uterine bleeding (AUB), infertility, and recurrent pregnancy
loss (RPL) [1-3]. The ever increasing value of diagnostic and operative
hysteroscopy for patients with AUB serves as an appropriate tribute to
Pantaleoni, who in 1869 described this procedure to look inside the
uterus and could visualize an endometrial polyp [4]. AUB is the single
most common reason for gynaecological referrals [5]. While there are
various benign reasons for AUB, abnormal peri- and post-menopausal
bleeding is associated with endometrial cancer in about 10% of cases
[6]. Transvaginal sonography (TVS) is a valuable screening method to
identify women with endometrial pathology, not only by measuring
endometrial thickness but also by accessing focal abnormalities within
the endometrial cavity, however, its value is limited in the endometrial
characterization because the image of endometrium is given in a gray
scale which makes interpretation difficult and less accurate, also
because although in post-menopausal women the presence of thick
endometrium (>5 mm) may predict some kind of pathology, the exact
lesion cannot be discriminated until biopsy is performed [7,8]. Also,
despite the diagnostic accuracy and mini-invasiveness of 3D
sonohysterography (3D SHG), it was suggest that it cannot be a
substitute of hysteroscopy in endometrial disease diagnosis, but it
could be considered as a good method of screening to address patients
to hysteroscopic confirmation [9]. Dilatation and curettage (D&C) has
traditionally been considered as standard for investigation of AUB,
however, it is a blind procedure that can miss a focal lesion like a polyp
or a localized pathological lesions. In one study, 60% of patients had
less than half the uterine cavity curetted and 16% had less a quarter.
Negative endometrial biopsy in women with persistent AUB should be
further investigated [10,11].
Uterine abnormalities are estimated to play a causal role in a
substantial number of couples seeking treatment for infertility and in
women with recurrent miscarriages whether of the first or second
trimester [12,13]. Their assumed pathophysiologycial mechanism is
that they impair proper embryo implantation and growth due to poor
vascularization with subsequent infertility or miscarriage [14]. The
rate of uterine anomalies is reported to be as 2-5% in women with a
good obstetric history or those at low risk for complications [15,16],
whereas more than 30% of infertile patients are reported to suffer from
abnormal intrauterine findings [17]. A wide discrepancy (from 6.3 to
67%) of the rate of anomalies has been described for patients with
recurrent pregnancy losses [16,18]. These findings mirror differences
in study designs and the variations of anomalies reported in the
respective studies [18].
Hysteroscopy is an accurate and less invasive method for the
evaluation of uterine cavity. It is a dynamic test and allows a direct
visualization of the endometrium, revealing the nature, location,
shape, size and vascular pattern of any uterine cavity abnormalities.
The main advantage of hysteroscopy is that biopsies can be taken at
Reproductive System & Sexual
Disorders Elbareg et al., Reprod Syst Sex Disord 2015, 4:2
http://dx.doi.org/10.4172/2161-038X.1000149
Research Article Open access journal
Reprod Syst Sex Disord
ISSN:2161-038X RSSD, an open access journal
Volume 4 • Issue 2 • 1000149
: Current Research
the same time with great safety, which improves the diagnostic
accuracy. Also, its "see and treat" potential provides higher patient
satisfaction. Hysteroscopy is increasingly replacing D&C for the
evaluation of AUB [19,20]. The objective of this study is to evaluate the
diagnostic accuracy of hysteroscopy in detection of uterine cavity
lesions compared with histopathological results of excised biopsy.
Subjects and Materials
A prospective study was carried out from Jan. 2010 to Jan. 2013.
Two hundred and eighty patients were referred with abnormal
ultrasonographic scanning (USS), AUB, infertility or RPL were
admitted into our gynecology departments at Misurata Central
Hospital. Patients underwent a preliminary assessment by history,
clinical examination and USS of the pelvis. Baseline laboratory
investigations included a complete blood count were also done. All
hysteroscopies were performed under general anaesthesia using video-
assisted diagnostic hysteroscopy with outer sheath 5.2 mm (Storz
GmbH, Germany). Pathology in the uterine cavity was treated at the
same setting using an operative hysteroscopic 10 mm fibreoptic
resectoscope (Storz GmbH, Germany). All procedure were video
recorded. The uterine cavity was expanded using distension media
(Glycine 1.5%) administrated via electronically controlled irrigation
delivery system (Endomate) (Storz GmbH, Germany).
Hysteroscopy was performed with a standard sequence, inspecting
ectocervix, endocervical canal, uterine cavity, endometrium and tubal
ostia. Hysteroscopic findings were allocated either to "the uterine
cavity lesions" or "the endometrial aspect characterization". The
uterine cavity lesions that were found including: endometrial polyp,
cervical polyp, myoma, endometrial adhesions, congenital
malformation, placental rest, lost intrauterine device (IUD). In the
endometrial aspect characterization, differentiation between
functional, atrophic or thin endometrium, dysfunctional,
endometritis, cystic atrophy, hyperplasia, polypoidal, and carcinoma
was done. The hysteroscopic observation was documented, and an
endometrial biopsy and/or the removal of the pathology was
performed. The histopathological results were used as gold standard
and compared with the hysteroscopic documented observation. The
sensitivity, specificity, and predictive value of hysteroscopy were
calculated. Statistical analysis was performed using SPSS software. The
P value was calculated by applying student t test, and considered to be
significant if (<0.05).
Results
In this study, 280 patients were recruited; the age ranges from 25-65
years with average of 45 years. Two hundred thirty patients (82.14%)
with abnormal findings on USS such as endometrial thickness,
endometrial irregularity, polyps, myomas, IUD, placental debris. The
remaining 50 patients (17.85%) had normal scan but referred because
of infertility (10 cases), (20 cases) of menorrhagia, (15 cases) of
postmenopausal bleeding, and (5 cases) were of cervical polyp. Uterine
cavity abnormalities were detected in 71.4% of patients, significantly
more at age of >30 years (58.3%) compared with that of <30 years
(34.6%) (P<0.05).
Regarding the uterine cavity lesions diagnosed by hysteroscopy-200
(71.4%) cases showed uterine abnormalities, out of them: 150 (53.6%)
cases of endometrial polyps were diagnosed, one of them associated
with endometrial carcinoma on histopathology result, some were
associated with cervical polyps and myomas. There were 25 cases of
Submucous myomas, 10 cases of cervical polyp, 3 of them were
associated with endometrial polyp. Septate and subseptate uterus were
found in 8 cases, one of them associated with endometrial polyp and
the other with cervical polyp. Endometrial adhesions were found in 13
(4.6%) cases, one was associated with myoma, one associated with
endometrial polyp and the other associated with cervical polyp. The
other diagnosed lesions included 6 cases of IUD (2.1%), 5 (1.7%) cases
of placental debris and 3 (1.07%) endometrial cysts. The remaining 80
(28.6%) cases did not have any uterine lesions on hysteroscopy.
Compared with histopathology, 105 (37.5%) cases did not show any
pathology, with false negative in 25 cases including, 10 cases of isolated
intrauterine adhesion, 6 cases of isolated septate uterus, and 5 cases of
isolated IUD, 1 case of destroyed cyst, and 3 cases of small myomas
were not submitted to biopsy (Figure 1).
Citation: Elbareg AM, Elmahashi MO, Essadi FM (2015) Evaluation of Intrauterine Pathology: Efficacy of Diagnostic Hysteroscopy in
Comparison to Histopathological Examination. Reprod Syst Sex Disord 4: 149. doi:10.4172/2161-038X.1000149
Page 2 of 6
Reprod Syst Sex Disord
ISSN:2161-038X RSSD, an open access journal
Volume 4 • Issue 2 • 1000149
Figure 1: The uterine cavity lesions in hysteroscopy and histopathology.
Regarding the endometrial aspect characterization- one case
(0.36%) of endometrial carcinoma was detected, 27 (9.6%) cases of
endometrial hyperplasia, 30 (10.7%) cases of dysfunctional
endometrium, 15 (5.3%) cases of polypoidal endometrium, 3 (1%)
cases of endometritis, 4 (1.4%) cases of cystic atrophic endometrium,
and 34 (12.1%) cases of atrophic endometrium. Functional
endometrium was found in 166 (59.2%) cases (Figure 2).
Citation: Elbareg AM, Elmahashi MO, Essadi FM (2015) Evaluation of Intrauterine Pathology: Efficacy of Diagnostic Hysteroscopy in
Comparison to Histopathological Examination. Reprod Syst Sex Disord 4: 149. doi:10.4172/2161-038X.1000149
Page 3 of 6
Reprod Syst Sex Disord
ISSN:2161-038X RSSD, an open access journal
Volume 4 • Issue 2 • 1000149
Figure 2: The endometrial aspect characterization by hysteroscopy, histopathology.
When compared with histopathological examination as gold
standard, hysteroscopy failed to diagnose the following uterine lesions:
one case of myoma that was really a polyp, two cases considered
without endometrial lesions that had polyps on histopathological
examination, the 2 polyps that were myomas. The hysteroscopy also
failed in the endometrial characterization of the following cases: 2
cases of carcinoma were wrongly diagnosed as hyperplasia, 1 complex
hyperplasia, 2 cases of dysfunctional endometrium, and 2 other
polypoid endometrium were wrongly classified as atrophic
endometrium.
The hysteroscopic evaluation was characterized as functional
endometrium, dysfunctional endometrium in 12 cases, polypoid
endometrium in 4 cases, simple hyperplasia in 1 case, and complex in
another. Considering the 26 false-positive diagnosis, these include 3
cases of focal hyperplasia that were atrophic endometrium, 7 cases of
polypoid endometrium, 6 cases of dysfunctional endometrium and 10
cases of hyperplasia that were all functional endometrium (Tables 1
and 2). Considering the diagnostic accuracy of hysteroscopy in the
evaluation of intra-cavity lesions, the sensitivity, specificity, positive
and negative predictive values were respectively 98.9%, 97.5%, 98.8%,
and 98.5%. The values of the same parameters regarding the
characterization of endometrium were as follow: 78.9%, 90.7%, 82.8%,
90.9%. The diagnostic accuracy was 98.3% for endometrial cavity
lesions and 87.8% for endometrial characterization. The incidence of
endometrial adenocarcinoma was 1.1%, the sensitivity and specificity
of hysteroscopy were respectively 60% and 99% with a diagnostic
accuracy of 99%. The incidence of endometrial hyperplasia was 9.6%,
hysteroscopy has sensitivity of 88% and a specificity of 90% with
diagnostic accuracy of 62%. The complication rate was 2%, including 2
cases of postoperative hemorrhage that were managed as in-patient for
24-h observation and then discharged, one perforation, 4 cases of false
route were managed conservatively. Four cases of endometrial
carcinoma (one in a polyp lesion) were submitted for hysterectomy
(Figure 3).
Citation: Elbareg AM, Elmahashi MO, Essadi FM (2015) Evaluation of Intrauterine Pathology: Efficacy of Diagnostic Hysteroscopy in
Comparison to Histopathological Examination. Reprod Syst Sex Disord 4: 149. doi:10.4172/2161-038X.1000149
Page 4 of 6
Reprod Syst Sex Disord
ISSN:2161-038X RSSD, an open access journal
Volume 4 • Issue 2 • 1000149
Hysteroscopic exam Histopathological exam False negative
hyperplasia Carcinoma 2
Functional Polypoid 4
Functional Hyperplasia 2
functional Dysfunctional 12
Atrophic Dysfunctional 2
Atrophic Polypoid 3
Atrophic Complex hyperplasia 1
Table 1: Failure of hysteroscopic diagnosis of endometrial
characterization (False negative).
Hysteroscopic exam Histopathological exam False positive
Hyperplasia Functional 10
Polypoid Functional 7
Dysfunctional Functional 6
Hyperplasia Atrophic 3
Table 2: Failure of hysteroscopic diagnosis of endometrial
characterization (False positive).
Figure 3: Different pathologies of endometrial cavity on
hysteroscopy.
Discussion
Hysteroscopic inspection of uterine cavity is a simple and well
accepted method for investigation of intrauterine pathology. The
direct visualization, real-time, real-color, hydrated, well-illuminated,
and augmented vision of the uterine cavity make this diagnostic tool
very accurate to detect minute focal endometrial pathology and small
lesions otherwise not possible, complemented to the ability of
performing guided direct biopsies and treatment on the same
diagnostic setting. Hysteroscopic examination may predict
endometrial lesions with a good accuracy as well as endometrial aspect
characterization, adopting a nomenclature similar to that used by the
pathologist. This approach makes correlation between hysteroscopic
findings and histopathological results easier.
In our study, hysteroscopic abnormalities in the uterine cavity were
seen in about 71.4% of cases. The accuracy of hysteroscopy to diagnose
uterine cavity lesions is better than that of endometrial
characterization (98.3% versus 87.8%). The false diagnosis was lower
and include: one case of hysteroscopic diagnosis of myoma that was a
polyp, two cases of polyps that were myomas on histopathological
examination. The false negative include two focal thicker lesions
interpreted as dysfunctional endometrium that were polyps on
histopathological examination. The false diagnosis on endometrium
characterization is a concern, particularly the false negative; 12 cases of
dysfunctional endometrium were misdiagnosed as functional
endometrium.
Dysfunctional endometrium means a discordant maturation
between endometrium and hormonal cycle, or a focal discordance
with focal areas in various phases of endometrial cycle at the same
time [21]. The two false negative for carcinoma occurred in
postmenopausal women. Both were diagnosed as hyperplasia but their
histopathological examination revealed atypical hyperplasia with focus
of adenocarcinoma. After hysterectomy, adenocarcinoma was
confirmed on histopathological examination. Hysteroscopic guided
biopsy permitted the correct histopathological diagnosis. Our study
showed that for endometrial cancer, hysteroscopy has sensitivity and
specificity of 60% and 99%% with a diagnostic accuracy of 99%. There
is continuing debate about the value and accuracy of hysteroscopy in
diagnosis of endometrial diseases that is endometrial cancer and its
precursor, endometrial hyperplasia. Previous studies showed that
hysteroscopy was more accurate in identifying intrauterine pathologies
like endometrial polyp, Submucous myoma and misplaced IUD than
endometrial biopsy or D&C alone, whereas diagnosis of hyperplasia,
its types and carcinoma was only possible after histopathological
examination [22-24]. In comparison with our study, some studies
showed an overall sensitivity and specificity of hysteroscopy for
endometrial cancer was 86.4% and 99.2% respectively [21]. The
conclusion of many studies was that hysteroscopy has high accuracy in
diagnosing endometrial cancer rather than excluding it, with high
accuracy in postmenopausal women rather than in premenopausal
[25-27]. Add to that it also demonstrates any possible involvement of
the lower uterine segment and cervix. Therefore, since the incidence of
focal lesions in patients with AUB is 47-74% [28] (71.4% in our study),
and the main purpose is to detect endometrial cancer, combined
hysteroscopy and biopsy [29-31] is considered to be the new gold
standard which showed an accuracy of almost 100% in diagnosis of
carcinoma and its precursors.
Citation: Elbareg AM, Elmahashi MO, Essadi FM (2015) Evaluation of Intrauterine Pathology: Efficacy of Diagnostic Hysteroscopy in
Comparison to Histopathological Examination. Reprod Syst Sex Disord 4: 149. doi:10.4172/2161-038X.1000149
Page 5 of 6
Reprod Syst Sex Disord
ISSN:2161-038X RSSD, an open access journal
Volume 4 • Issue 2 • 1000149
Conclusion
Hysteroscopy is a safe and reliable procedure for evaluating benign
endometrial lesion, allows direct visualization of uterine cavity and
this particularly confer it a high diagnostic accuracy, that associated to
the possibility of simultaneous treatment or biopsy procedures gives it
an irreplaceable value in diagnosis and treatment of intrauterine
disease.
References
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Citation: Elbareg AM, Elmahashi MO, Essadi FM (2015) Evaluation of Intrauterine Pathology: Efficacy of Diagnostic Hysteroscopy in
Comparison to Histopathological Examination. Reprod Syst Sex Disord 4: 149. doi:10.4172/2161-038X.1000149
Page 6 of 6
Reprod Syst Sex Disord
ISSN:2161-038X RSSD, an open access journal
Volume 4 • Issue 2 • 1000149

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Evaluation of intrauterine pathology efficacy of diagnostic hysteroscopy in histopathological examination

  • 1. Evaluation of Intrauterine Pathology: Efficacy of Diagnostic Hysteroscopy in Comparison to Histopathological Examination Aisha M Elbareg*, Mohamed O Elmahashi and Fathi M Essadi Gynecology Department, Misurata Central Hospital/Misurata University, Libyan Arab Jamahiriya, Libya *Corresponding author: Aisha M Elbareg Gynecology Department, Misurata Central Hospital/Misurata University, Libya, Tel: 00218914213607; E-mail: elbaregsm@hotmail.com Received date: April 03, 2015, Accepted date: April 21, 2015, Published date: April 25, 2015 Copyright: © 2015 Elbareg AM, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Abstract The aim of this work is to evaluate the diagnostic accuracy of hysteroscopy compared to histopathological findings in cases with intrauterine pathology. This prospective clinical trial was carried out over a period of two years. 280 patients were recruited with an average of 45 years (range: 25-65 years). Two hundred and thirty patients (82.14%) with abnormal findings in ultrasound examinations, the remaining 50 (17.85%) had normal scan, referred mainly because of abnormal uterine bleeding (AUB) and infertility. Hysteroscopic findings divided into; uterine cavity lesions: endometrial or cervical polyps, myomas, cysts, placental derbis, adhesions, congenital malformations and IUCD retention, endometrial characterization including: functional, dysfunctional, atrophic endometrium, hyperplasia, polypoid and carcinoma. Biopsies or removal of pathology were performed and sent for histopathology examinations, results were compared with hysteroscopic findings. Sensitivity, Specificity and predictive value (PV) of hysteroscopy were calculated. Results: uterine cavity abnormalities were detected in (71.4%) patients, significantly more at ages of >30 years (58.3%) compared with ages of <30 years (34.6%) (P<0.05). In benign endometrial lesions, the sensitivity of hysteroscopy was (98.9%), specificity was (97.5%), positive predictive value was (98.8%), negative predictive value was (98.5%) with diagnostic accuracy of 98.3%, same parameters for endometrial characterization: (78.9%), (90.7%), (82.8%), (90.9%) with diagnostic accuracy of 87.8%. Conclusions: Hysteroscopy allows direct visualization of uterine cavity, it is a safe and reliable procedure for evaluating benign endometrial lesion, but in view of poor validity to exclude endometrial hyperplasia and cancer, it is recommended always to perform diagnostic hysteroscopy combined with biopsy procedures, giving it an irreplaceable value in diagnosis and treatment of intrauterine disease. Keywords: Hysteroscopy; Abnormal uterine bleeding; Infertility; Endometrial pathology Introduction During the last decade hysteroscopy has become the tool of choice for the evaluation of the endometrial cavity including assessment of abnormal uterine bleeding (AUB), infertility, and recurrent pregnancy loss (RPL) [1-3]. The ever increasing value of diagnostic and operative hysteroscopy for patients with AUB serves as an appropriate tribute to Pantaleoni, who in 1869 described this procedure to look inside the uterus and could visualize an endometrial polyp [4]. AUB is the single most common reason for gynaecological referrals [5]. While there are various benign reasons for AUB, abnormal peri- and post-menopausal bleeding is associated with endometrial cancer in about 10% of cases [6]. Transvaginal sonography (TVS) is a valuable screening method to identify women with endometrial pathology, not only by measuring endometrial thickness but also by accessing focal abnormalities within the endometrial cavity, however, its value is limited in the endometrial characterization because the image of endometrium is given in a gray scale which makes interpretation difficult and less accurate, also because although in post-menopausal women the presence of thick endometrium (>5 mm) may predict some kind of pathology, the exact lesion cannot be discriminated until biopsy is performed [7,8]. Also, despite the diagnostic accuracy and mini-invasiveness of 3D sonohysterography (3D SHG), it was suggest that it cannot be a substitute of hysteroscopy in endometrial disease diagnosis, but it could be considered as a good method of screening to address patients to hysteroscopic confirmation [9]. Dilatation and curettage (D&C) has traditionally been considered as standard for investigation of AUB, however, it is a blind procedure that can miss a focal lesion like a polyp or a localized pathological lesions. In one study, 60% of patients had less than half the uterine cavity curetted and 16% had less a quarter. Negative endometrial biopsy in women with persistent AUB should be further investigated [10,11]. Uterine abnormalities are estimated to play a causal role in a substantial number of couples seeking treatment for infertility and in women with recurrent miscarriages whether of the first or second trimester [12,13]. Their assumed pathophysiologycial mechanism is that they impair proper embryo implantation and growth due to poor vascularization with subsequent infertility or miscarriage [14]. The rate of uterine anomalies is reported to be as 2-5% in women with a good obstetric history or those at low risk for complications [15,16], whereas more than 30% of infertile patients are reported to suffer from abnormal intrauterine findings [17]. A wide discrepancy (from 6.3 to 67%) of the rate of anomalies has been described for patients with recurrent pregnancy losses [16,18]. These findings mirror differences in study designs and the variations of anomalies reported in the respective studies [18]. Hysteroscopy is an accurate and less invasive method for the evaluation of uterine cavity. It is a dynamic test and allows a direct visualization of the endometrium, revealing the nature, location, shape, size and vascular pattern of any uterine cavity abnormalities. The main advantage of hysteroscopy is that biopsies can be taken at Reproductive System & Sexual Disorders Elbareg et al., Reprod Syst Sex Disord 2015, 4:2 http://dx.doi.org/10.4172/2161-038X.1000149 Research Article Open access journal Reprod Syst Sex Disord ISSN:2161-038X RSSD, an open access journal Volume 4 • Issue 2 • 1000149 : Current Research
  • 2. the same time with great safety, which improves the diagnostic accuracy. Also, its "see and treat" potential provides higher patient satisfaction. Hysteroscopy is increasingly replacing D&C for the evaluation of AUB [19,20]. The objective of this study is to evaluate the diagnostic accuracy of hysteroscopy in detection of uterine cavity lesions compared with histopathological results of excised biopsy. Subjects and Materials A prospective study was carried out from Jan. 2010 to Jan. 2013. Two hundred and eighty patients were referred with abnormal ultrasonographic scanning (USS), AUB, infertility or RPL were admitted into our gynecology departments at Misurata Central Hospital. Patients underwent a preliminary assessment by history, clinical examination and USS of the pelvis. Baseline laboratory investigations included a complete blood count were also done. All hysteroscopies were performed under general anaesthesia using video- assisted diagnostic hysteroscopy with outer sheath 5.2 mm (Storz GmbH, Germany). Pathology in the uterine cavity was treated at the same setting using an operative hysteroscopic 10 mm fibreoptic resectoscope (Storz GmbH, Germany). All procedure were video recorded. The uterine cavity was expanded using distension media (Glycine 1.5%) administrated via electronically controlled irrigation delivery system (Endomate) (Storz GmbH, Germany). Hysteroscopy was performed with a standard sequence, inspecting ectocervix, endocervical canal, uterine cavity, endometrium and tubal ostia. Hysteroscopic findings were allocated either to "the uterine cavity lesions" or "the endometrial aspect characterization". The uterine cavity lesions that were found including: endometrial polyp, cervical polyp, myoma, endometrial adhesions, congenital malformation, placental rest, lost intrauterine device (IUD). In the endometrial aspect characterization, differentiation between functional, atrophic or thin endometrium, dysfunctional, endometritis, cystic atrophy, hyperplasia, polypoidal, and carcinoma was done. The hysteroscopic observation was documented, and an endometrial biopsy and/or the removal of the pathology was performed. The histopathological results were used as gold standard and compared with the hysteroscopic documented observation. The sensitivity, specificity, and predictive value of hysteroscopy were calculated. Statistical analysis was performed using SPSS software. The P value was calculated by applying student t test, and considered to be significant if (<0.05). Results In this study, 280 patients were recruited; the age ranges from 25-65 years with average of 45 years. Two hundred thirty patients (82.14%) with abnormal findings on USS such as endometrial thickness, endometrial irregularity, polyps, myomas, IUD, placental debris. The remaining 50 patients (17.85%) had normal scan but referred because of infertility (10 cases), (20 cases) of menorrhagia, (15 cases) of postmenopausal bleeding, and (5 cases) were of cervical polyp. Uterine cavity abnormalities were detected in 71.4% of patients, significantly more at age of >30 years (58.3%) compared with that of <30 years (34.6%) (P<0.05). Regarding the uterine cavity lesions diagnosed by hysteroscopy-200 (71.4%) cases showed uterine abnormalities, out of them: 150 (53.6%) cases of endometrial polyps were diagnosed, one of them associated with endometrial carcinoma on histopathology result, some were associated with cervical polyps and myomas. There were 25 cases of Submucous myomas, 10 cases of cervical polyp, 3 of them were associated with endometrial polyp. Septate and subseptate uterus were found in 8 cases, one of them associated with endometrial polyp and the other with cervical polyp. Endometrial adhesions were found in 13 (4.6%) cases, one was associated with myoma, one associated with endometrial polyp and the other associated with cervical polyp. The other diagnosed lesions included 6 cases of IUD (2.1%), 5 (1.7%) cases of placental debris and 3 (1.07%) endometrial cysts. The remaining 80 (28.6%) cases did not have any uterine lesions on hysteroscopy. Compared with histopathology, 105 (37.5%) cases did not show any pathology, with false negative in 25 cases including, 10 cases of isolated intrauterine adhesion, 6 cases of isolated septate uterus, and 5 cases of isolated IUD, 1 case of destroyed cyst, and 3 cases of small myomas were not submitted to biopsy (Figure 1). Citation: Elbareg AM, Elmahashi MO, Essadi FM (2015) Evaluation of Intrauterine Pathology: Efficacy of Diagnostic Hysteroscopy in Comparison to Histopathological Examination. Reprod Syst Sex Disord 4: 149. doi:10.4172/2161-038X.1000149 Page 2 of 6 Reprod Syst Sex Disord ISSN:2161-038X RSSD, an open access journal Volume 4 • Issue 2 • 1000149
  • 3. Figure 1: The uterine cavity lesions in hysteroscopy and histopathology. Regarding the endometrial aspect characterization- one case (0.36%) of endometrial carcinoma was detected, 27 (9.6%) cases of endometrial hyperplasia, 30 (10.7%) cases of dysfunctional endometrium, 15 (5.3%) cases of polypoidal endometrium, 3 (1%) cases of endometritis, 4 (1.4%) cases of cystic atrophic endometrium, and 34 (12.1%) cases of atrophic endometrium. Functional endometrium was found in 166 (59.2%) cases (Figure 2). Citation: Elbareg AM, Elmahashi MO, Essadi FM (2015) Evaluation of Intrauterine Pathology: Efficacy of Diagnostic Hysteroscopy in Comparison to Histopathological Examination. Reprod Syst Sex Disord 4: 149. doi:10.4172/2161-038X.1000149 Page 3 of 6 Reprod Syst Sex Disord ISSN:2161-038X RSSD, an open access journal Volume 4 • Issue 2 • 1000149
  • 4. Figure 2: The endometrial aspect characterization by hysteroscopy, histopathology. When compared with histopathological examination as gold standard, hysteroscopy failed to diagnose the following uterine lesions: one case of myoma that was really a polyp, two cases considered without endometrial lesions that had polyps on histopathological examination, the 2 polyps that were myomas. The hysteroscopy also failed in the endometrial characterization of the following cases: 2 cases of carcinoma were wrongly diagnosed as hyperplasia, 1 complex hyperplasia, 2 cases of dysfunctional endometrium, and 2 other polypoid endometrium were wrongly classified as atrophic endometrium. The hysteroscopic evaluation was characterized as functional endometrium, dysfunctional endometrium in 12 cases, polypoid endometrium in 4 cases, simple hyperplasia in 1 case, and complex in another. Considering the 26 false-positive diagnosis, these include 3 cases of focal hyperplasia that were atrophic endometrium, 7 cases of polypoid endometrium, 6 cases of dysfunctional endometrium and 10 cases of hyperplasia that were all functional endometrium (Tables 1 and 2). Considering the diagnostic accuracy of hysteroscopy in the evaluation of intra-cavity lesions, the sensitivity, specificity, positive and negative predictive values were respectively 98.9%, 97.5%, 98.8%, and 98.5%. The values of the same parameters regarding the characterization of endometrium were as follow: 78.9%, 90.7%, 82.8%, 90.9%. The diagnostic accuracy was 98.3% for endometrial cavity lesions and 87.8% for endometrial characterization. The incidence of endometrial adenocarcinoma was 1.1%, the sensitivity and specificity of hysteroscopy were respectively 60% and 99% with a diagnostic accuracy of 99%. The incidence of endometrial hyperplasia was 9.6%, hysteroscopy has sensitivity of 88% and a specificity of 90% with diagnostic accuracy of 62%. The complication rate was 2%, including 2 cases of postoperative hemorrhage that were managed as in-patient for 24-h observation and then discharged, one perforation, 4 cases of false route were managed conservatively. Four cases of endometrial carcinoma (one in a polyp lesion) were submitted for hysterectomy (Figure 3). Citation: Elbareg AM, Elmahashi MO, Essadi FM (2015) Evaluation of Intrauterine Pathology: Efficacy of Diagnostic Hysteroscopy in Comparison to Histopathological Examination. Reprod Syst Sex Disord 4: 149. doi:10.4172/2161-038X.1000149 Page 4 of 6 Reprod Syst Sex Disord ISSN:2161-038X RSSD, an open access journal Volume 4 • Issue 2 • 1000149
  • 5. Hysteroscopic exam Histopathological exam False negative hyperplasia Carcinoma 2 Functional Polypoid 4 Functional Hyperplasia 2 functional Dysfunctional 12 Atrophic Dysfunctional 2 Atrophic Polypoid 3 Atrophic Complex hyperplasia 1 Table 1: Failure of hysteroscopic diagnosis of endometrial characterization (False negative). Hysteroscopic exam Histopathological exam False positive Hyperplasia Functional 10 Polypoid Functional 7 Dysfunctional Functional 6 Hyperplasia Atrophic 3 Table 2: Failure of hysteroscopic diagnosis of endometrial characterization (False positive). Figure 3: Different pathologies of endometrial cavity on hysteroscopy. Discussion Hysteroscopic inspection of uterine cavity is a simple and well accepted method for investigation of intrauterine pathology. The direct visualization, real-time, real-color, hydrated, well-illuminated, and augmented vision of the uterine cavity make this diagnostic tool very accurate to detect minute focal endometrial pathology and small lesions otherwise not possible, complemented to the ability of performing guided direct biopsies and treatment on the same diagnostic setting. Hysteroscopic examination may predict endometrial lesions with a good accuracy as well as endometrial aspect characterization, adopting a nomenclature similar to that used by the pathologist. This approach makes correlation between hysteroscopic findings and histopathological results easier. In our study, hysteroscopic abnormalities in the uterine cavity were seen in about 71.4% of cases. The accuracy of hysteroscopy to diagnose uterine cavity lesions is better than that of endometrial characterization (98.3% versus 87.8%). The false diagnosis was lower and include: one case of hysteroscopic diagnosis of myoma that was a polyp, two cases of polyps that were myomas on histopathological examination. The false negative include two focal thicker lesions interpreted as dysfunctional endometrium that were polyps on histopathological examination. The false diagnosis on endometrium characterization is a concern, particularly the false negative; 12 cases of dysfunctional endometrium were misdiagnosed as functional endometrium. Dysfunctional endometrium means a discordant maturation between endometrium and hormonal cycle, or a focal discordance with focal areas in various phases of endometrial cycle at the same time [21]. The two false negative for carcinoma occurred in postmenopausal women. Both were diagnosed as hyperplasia but their histopathological examination revealed atypical hyperplasia with focus of adenocarcinoma. After hysterectomy, adenocarcinoma was confirmed on histopathological examination. Hysteroscopic guided biopsy permitted the correct histopathological diagnosis. Our study showed that for endometrial cancer, hysteroscopy has sensitivity and specificity of 60% and 99%% with a diagnostic accuracy of 99%. There is continuing debate about the value and accuracy of hysteroscopy in diagnosis of endometrial diseases that is endometrial cancer and its precursor, endometrial hyperplasia. Previous studies showed that hysteroscopy was more accurate in identifying intrauterine pathologies like endometrial polyp, Submucous myoma and misplaced IUD than endometrial biopsy or D&C alone, whereas diagnosis of hyperplasia, its types and carcinoma was only possible after histopathological examination [22-24]. In comparison with our study, some studies showed an overall sensitivity and specificity of hysteroscopy for endometrial cancer was 86.4% and 99.2% respectively [21]. The conclusion of many studies was that hysteroscopy has high accuracy in diagnosing endometrial cancer rather than excluding it, with high accuracy in postmenopausal women rather than in premenopausal [25-27]. Add to that it also demonstrates any possible involvement of the lower uterine segment and cervix. Therefore, since the incidence of focal lesions in patients with AUB is 47-74% [28] (71.4% in our study), and the main purpose is to detect endometrial cancer, combined hysteroscopy and biopsy [29-31] is considered to be the new gold standard which showed an accuracy of almost 100% in diagnosis of carcinoma and its precursors. Citation: Elbareg AM, Elmahashi MO, Essadi FM (2015) Evaluation of Intrauterine Pathology: Efficacy of Diagnostic Hysteroscopy in Comparison to Histopathological Examination. Reprod Syst Sex Disord 4: 149. doi:10.4172/2161-038X.1000149 Page 5 of 6 Reprod Syst Sex Disord ISSN:2161-038X RSSD, an open access journal Volume 4 • Issue 2 • 1000149
  • 6. Conclusion Hysteroscopy is a safe and reliable procedure for evaluating benign endometrial lesion, allows direct visualization of uterine cavity and this particularly confer it a high diagnostic accuracy, that associated to the possibility of simultaneous treatment or biopsy procedures gives it an irreplaceable value in diagnosis and treatment of intrauterine disease. References 1. Pop-Trajković-Dinić S, Ljubić A, Kopitović V, Antić V, Stamenović S, et al. (2013) The role of hysteroscopy in diagnosis and treatment of postmenopausal bleeding. Vojnosanit Pregl 70: 747-750. 2. Makled AK, Farghali MM, Shenouda DS (2014) Role of hysteroscopy and endometrial biopsy in women with unexplained infertility. Arch Gynecol Obstet 289: 187-192. 3. Yang R, Du X, Wang Y, Song X, Yang Y, et al. (2014) The hysteroscopy and histological diagnosis and treatment value of chronic endometritis in recurrent implantation failure patients. Arch Gynecol Obstet 289: 1363-1369. 4. Pantoleoni D (1869) On endoscopic examination of the cavity of the womb. Med. Press. Cire 8: 26. 5. Gimpelson RJ, Rappold HO (1988) A comparative study between panoramic hysteroscopy with directed biopsies and dilatation and curettage. A review of 276 cases. Am J Obstet Gynecol 158: 489-492. 6. Creasman WT (1997) Endometrial cancer: incidence, prognostic factors, diagnosis, and treatment. Semin Oncol 24: S1-140-S1-50. 7. Luterek K, Szymusik I, Bartkowiak R, Wielgos M (2014) Sonohysterography in peri- and postmenopausal women with abnormal uterine bleeding or abnormal endometrial appearance. Neuro Endocrinol Lett 35: 297-300. 8. BTV, Shivalingaiah N (2014) Role of transvaginal sonography and diagnostic hysteroscopy in abnormal uterine bleeding. J Clin Diagn Res 8: OC06-08. 9. Laganà AS, Ciancimino L, Mancuso A, Chiofalo B, Rizzo P, et al. (2014) 3D sonohysterography vs hysteroscopy: a cross-sectional study for the evaluation of endouterine diseases. Arch Gynecol Obstet 290: 1173-1178. 10. Leather AT, Savvas M, Studd WW (1991) Endometrial histology and bleeding patterns after 8 years of continuous combined estrogen and progesterone therapy in postmenopausal women. Obstet. Gynecol 78: 1008-1010. 11. Kotdawala P, Kotdawala S, Nagar N (2013) Evaluation of endometrium in peri-menopausal abnormal uterine bleeding. J Midlife Health 4: 16-21. 12. Wallach EE (1972) The uterine factor in infertility. Fertil Steril 23: 138-158. 13. Propst AM, Hill JA 3rd (2000) Anatomic factors associated with recurrent pregnancy loss. Semin Reprod Med 18: 341-350. 14. Brown SE, Coddington CC, Schnorr J, Toner JP, Gibbons W, et al. (2000) Evaluation of outpatient hysteroscopy, saline infusion hysterosonography, and hysterosalpingography in infertile women: a prospective, randomized study. Fertil. Steril 74: 1029–1034. 15. Ashton D, Amin HK, Richart RM, Neuwirth RS (1988) The incidence of asymptomatic uterine anomalies in women undergoing transcervical tubal sterilization. Obstet Gynecol 72: 28-30. 16. Salim R, Regan L, Woelfer B, Backos M, Jurkovic D (2003) A comparative study of the morphology of congenital uterine anomalies in women with and without a history of recurrent first trimester miscarriage. Hum Reprod 18: 162-166. 17. Hornemann A, Luedders DW, Kumbartski M (2009) Anatomic disorders as a reason for recurrent miscarriages. Gynakologe 42: 11–16. 18. Weiss A, Shalev E, Romano S (2005) Hysteroscopy may be justified after two miscarriages. Hum Reprod 20: 2628-2631. 19. Wieser F, Tempfer C, Kurz C, Nagele F (2001) Hysteroscopy in 2001: a comprehensive review. Acta Obstet Gynecol Scand 80: 773-783. 20. Loiacono RM, Trojano G, Del Gaudio N, Kardhashi A, Deliso MA, et al. 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Panda A, Parulekar SV, Gupta A (1999) Diagnostic hysteroscopy in abnormal uterine bleeding and histopathological correlation. J Obstetgynecol 49: 74-76 26. Sheetal P, Patil SG, BhuteSB, Inamdar SA (2009) Role of diagnostic hysteroscopy in abnormal uterine bleeding and its histopathological correlation. Journal of Gynecological Endoscopy and Surgery. 27. De Marchi F, Fabris AM, Tommasi L, Nappi L, Saccardi C, et al. (2014) Accuracy of hysteroscopy made by young residents in detecting endometrial pathologies in postmenopausal women. Eur J Gynaecol Oncol 35: 219-223. 28. Lasmar RB, Barrozo PR, de Oliveira MA, Coutinho ES, Dias R (2006) Validation of hysteroscopic view in cases of endometrial hyperplasia and cancer in patients with abnormal uterine bleeding. J Minim Invasive Gynecol 13: 409-412. 29. Koutlaki N, Dimitraki M (2010) Hysteroscopy and endometrial cancer. Diagnosis and influence on prognosis. Gynecol Surg 7:335-341. 30. Gan DE, Jawan RA, Moy FM (2013) Concordance between hysteroscopic impression and endometrial histopathological diagnosis. Prev Med 57 Suppl: S21-23. 31. 31.Pal L, Lapensee L, Toth TL, Isaacson KB (1997) Comparison of office hysteroscopy, transvaginal ultrasonography and endometrial biopsy in evaluation of abnormal uterine bleeding. JSLS 1: 125-130. Citation: Elbareg AM, Elmahashi MO, Essadi FM (2015) Evaluation of Intrauterine Pathology: Efficacy of Diagnostic Hysteroscopy in Comparison to Histopathological Examination. Reprod Syst Sex Disord 4: 149. doi:10.4172/2161-038X.1000149 Page 6 of 6 Reprod Syst Sex Disord ISSN:2161-038X RSSD, an open access journal Volume 4 • Issue 2 • 1000149