Skip to main content
Medical Science Monitor: International Medical Journal of Experimental and Clinical Research logoLink to Medical Science Monitor: International Medical Journal of Experimental and Clinical Research
. 2015 Dec 10;21:3860–3867. doi: 10.12659/MSM.895227

Analysis of Sensitivity, Specificity, and Positive and Negative Predictive Values of Smear and Colposcopy in Diagnosis of Premalignant and Malignant Cervical Lesions

Mert Ulaş Barut 1,A,B,C,D,E,F,G,, Ahmet Kale 2,A, Umur Kuyumcuoğlu 3,A, Murat Bozkurt 4,C,E,F, Elif Ağaçayak 5,C,G, Server Özekinci 6,G, Talip Gul 5,A
PMCID: PMC4678924  PMID: 26655816

Abstract

Background

This study aimed to examine the positive and negative predictive value in the diagnosis of premalignant and malignant lesions of cervical colposcopy, the sensitivity and specificity of smear, and to evaluate the correlation with histopathology of abnormal cytology and colposcopy.

Material/Methods

The criteria for inclusion of patients with unhealthy cervix in the study were: Erosion, Chronic cervicitis, and Healed lacerations, Hypertrophied cervix, bleeding on touch, suspicious growth/ulcer/polyp on the cervix, and abnormal discharges from the cervix. Women with frank carcinoma cervix, pregnant females, patients with bleeding per vaginum at the time of examination, and those who had used vaginal medications, vaginal contraceptives or douches in the last 48 h of examination were excluded from the study.

Demographic analysis was performed for 450 patients who were admitted to the clinic. Sensitivity, specificity, positive predictive value and negative predictive values of patients to identify cervical pathologies of smear and colposcopy were histopathologically calculated. The statistical software package SPSS 15.0 (SPSS Inc., Chicago, IL, USA) and Spearman‘s and Chi-Square tests were used for statistical analysis.

Results

Sensitivity, specificity, PPD and NDP of smear were 0.57%, 0.76%, 0.26%, 0.92% respectively. Sensitivity, specificity, PPD and NDP of colposcopy were 0.92%, 0.67%, 0.52%, 0.96% respectively. A statistically significant correlation was found between abnormal cytology and histopathology, and abnormal colposcopy finding and histopathology.

Conclusions

Women with clinical diagnosis of unhealthy cervix should be evaluated by cytology to detect any premalignant or malignant lesions. It was concluded that Pap smear, colposcopy and histopathology should be collectively evaluated to evaluate cervical findings in low socio-economic regions.

MeSH Keywords: Colposcopy, Cytological Techniques, Uterine Cervical Neoplasms

Background

Cervical cancer is one of the biggest health problems of women around the world [1]. Premalignant lesions are characterized by abnormal cellular or epithelial architecture in the areas surrounding the junction between the squamous and columnar epithelium (transformation zone) of the uterine cervix [2].

Papanicolaou (Pap) smear cytology has remained an important tool in the screening for cervical cancer [3]. Ideally, all patients with abnormal Papanicolaou smear cytology results should undergo colposcopic examination [4].The current evidence prefers reflex human papillomavirus (HPV) testing for women with atypical squamous cells of undetermined significance (ASCUS) cytology test results. However, for women with HPV-positive ASCUS, whether from reflex HPV testing or co-testing, and women with low-grade squamous intraepithelial lesion (LSIL) cytology test results and no HPV test or a positive HPV test result, colposcopy is recommended [5]. Further, in women with a histologic diagnosis of cervical intraepithelial neoplasia (CIN) 2, CIN 3, or CIN 2/3 and adequate colposcopic examination, both excision and ablation are acceptable treatment modalities, except in pregnant women and young women [4]. CIN I corresponded to mild dysplasia, CIN II to moderate dysplasia, and CIN III corresponded to both severe dysplasia and CIS. Thus, in 1990, a histopathological terminology based on two grades of disease was proposed: low-grade CIN comprising the abnormalities consistent with koilocytic atypia and CIN I lesions and high-grade CIN comprising CIN II and III. The high-grade lesions were considered true precursors of invasive cancer [6].

2001 Bethesda System is the most commonly used and most widely accepted classification to report cervical smear samples. In Bethesda System, squamous epithelial cell abnormality is divided into five categories including Atypical Squamous Cells of Undetermined Significance (ASC-US), Atypical squamous cells – cannot exclude HSIL (ASC-H), Low grade squamous intraepithelial lesion (LSIL), High grade squamous intraepithelial lesion (HSIL) and Squamous cell carcinoma (SCC). In this system, mild dysplasia (CIN I) patients are included in LSIL, while moderate (CIN II) and severe (CIN III) dysplasia patients are included in HSIL. On the other hand, glandular epithelial abnormalities are divided into three categories including Atypical Glandular Cells not otherwise specified (AGC), endocervical in situ adenocarcinoma (AIS), adenocarcinoma (endocervical, endometrial, extrauterine and non-specified [7]. Low sensitivity of cervical smear, the cost of colposcopy and invasiveness of histopathology are the handicaps for the evaluation of lesions. Furthermore, the objective is early and accurate diagnosis of pre-malign lesions. A review of the literature found that sensitivity, specificity, PPV and NPV values of smear, colposcopy and histopathological evaluation had wide ranges. This study was carried out to evaluate these screening and diagnosis tests in a tertiary healthcare center on a patient group with low socio-economic status in a developing region in Turkey. In this context, we aimed to analyze cyto-histopathological correlations in patients with diagnosis distribution and tissue diagnosis in cervical smear samples reported to be in the epithelial cell abnormality category. Sensitivity, specificity, PPV and NPV values for Pap smear, colposcopy, and histopathology were analyzed. We aimed to evaluate the correlation of abnormal cytology and colposcopy with histopathology.

Material and Methods

The study included a total of 450 married women clinically diagnosed with unhealthy cervix who were referred to colposcopy unit of Dicle University Faculty of Medicine. Ethics committee report was received from hospital local ethics committee and informed consent of for were received from the patients. All of the patients were asked questions about their history including age, occupation, number of pregnancy, contraception method (condom, the use of OKS-RIA, coitus interruptus, depo Provera), educational status and smoking. The criteria for inclusion of patients with unhealthy cervix in the study were: Erosion, Chronic cervicitis, and Healed lacerations, Hypertrophied cervix, bleeding on touch, suspicious growth/ulcer/polyp on the cervix and Abnormal discharges from the cervix. Women with frank carcinoma cervix, pregnant females, patients with bleeding per vaginum at the time of examination and those who had used vaginal medications, vaginal contraceptives or douches in the last 48 h of examination were excluded from the study. Acetowhite area, atypical vascularization, punctuation and mosaicism were evaluated in colposcopic analysis.

Smear collection technique

After taking a detailed history and doing thorough clinical examination, Pap smear was taken using conventional method for cervical cytology in all the patients. After asking the patient to empty the urinary bladder, they were put on the examination table in dorsal position and speculum was introduced into the vagina to expose the cervix. A Medscand Cell Sampling Kit (manufactured by Medscand Medical AB, Sweden) was used for taking cervical cytology. The endocervical cell sampling was done by using the cytobrush which was introduced into the cervical os along its axis till few bristles remained outside the os. The brush was rotated by 180o, maintaining the contact with the cervical canal. The sample was unrolled onto the slide in the opposite direction from which it was collected by twirling the handle of the brush. The slide was fixed immediately in 95% ethyl alcohol in Coplin’s jar. Next, the pointed end of the plastic Colin’s Ayres spatula was introduced into the cervical os and rotated 360° about the circumference of the os maintaining constant contact with the ectocervix and both surfaces of the spatula were smeared on a new slide and fixed immediately. After this, using the blunt end of the Ayres spatula, sample was taken from the posterior fornix and the material obtained was spread on a next slide and fixed immediately. All the three slides obtained were numbered as 1, 2 and 3 in the sequence in which they were prepared. After fixing, the slides were sent to the Pathology Department, stained with the Papanicolaou staining method [8]. Reporting of the slides was done according to The 2001 Bethesda system [9] by the consultant pathologist as follows.

Colposcopy technique

Sub-epithelial vascular structures were examined by damping the cervix with 10 cc serum physiologic. After applying 5% acetic acid solution, Leisegang brand BG/LED model was connected to the monitor and the cervix was analyzed using binocular colposcope (Model 1DW-LED) that comes with a drum changer with a magnification of 7.5/15/30, a convenient angular insight of 45 and is equipped with an extremely bright LED lighting.

Statistical evaluation

The statistical software package SPSS 15.0 (SPSS Inc., Chicago, IL, USA) and Spearman’s and Chi-Square tests were used for statistical analysis.

Results

Table 1: Pap test results of all patients were evaluated. Smear results of 394 patients (87.5%) were ‘Normal’, 29 patients (6.4%) were ‘ASCUS, 17 patients (3.8%) were ‘LGSİL’, 7 patients (1.6%) were ‘HGSIL’, 1 patient (0.2%) was AGUS, 2 patients (0.4%) were ‘Epidermoid ca’.

Table 1.

Pap Test results of all patients.

Smear results N %
Normal 394 87.5
ASCUS 29 6.4
LGSIL 17 3.8
HGSIL 7 1.6
AGUS 1 0.2
Epidermoid CA 2 0.4
Total 450 100.0

In Table 2, of a total of 450 patients, 226 (%50.2) had normal, 97 (% 21.6) had abnormal, 76 (%16.9) had ectropion, 45 (%10) had chronic cervicitis, 6 (%1.3) had cervical Tm.

Table 2.

Distribution of patients according to colposcopy findings.

Colposcopy findings N %
Normal 226 50.2
Abnormal 97 21.6
Ectropion 76 21.6
Chronic cervicitis 45 10.0
Cervical tm. 6 1.3

In Table 3, of a total of 450 patients 97 (21.6%) were found to have abnormal colposcopy findings. Of these patients, 18.5% had atypical vascularization, 16.4% had acetowhite epithelial + punctuation, 14.4% had atypical vascularization + punctuation, 10.3% had atypical vascularization + acetowhite epithelium, 10.3% had punctuation, 5.1% had acetowhite epithelium + punctuation + mosaicism, 4.1% had acetowhite epithelium + punctuation + mosaicism + atypical vascularization.

Table 3.

Distribution of patients according to abnormal colposcopy findings.

Abnormal colposcopy findings N:97 %
Atypical vascularization 18 0.185
Atypical vascularization + acetowhite epithelial 10 0.103
Atypical vascularization + punctuation 14 0.144
Acetowhite epithelial 12 0.123
Acetowhite epithelial + punctuation 16 0.164
Acetowhite epithelial + punctuation + mosaicism 5 0.051
Punctuation + mosaicism 4 0.041
Acetowhite epithelial + punctuation + mosaicism + atypical vascularization 4 0.041
Punctuation 10 0.103
Total 97 100.0

There was statistically significant correlation between abnormal cytology and histopathology (r=0.273, p=0.000 p<0.05). There was a statistically significant correlation between abnormal colposcopy finding and histopathology (r=0.613, p=0.002, p<0.05). Spearman’s correlation test. Recommended examination and treatment to our patients have been shown in Table 4.

Table 4.

Recommended examination and treatment.

Recommended examination and treatment N %
Local treatment + follow-up 320 71.1
LEEP + endocervical curettage 57 12.7
Conization + fractional curettage 38 8.4
Directed cervical punch biopsy + polypectomy 32 7.1
Refused the necessary treatment 3 0.7
Total 450 100.0

Discussion

Cancer of the cervix is a preventable disorder as the different screening, diagnostic and therapeutic procedures are effective. One of the essential responsibilities of the gynecologist is to detect neoplasm of the genital tract at the earliest. Since the introduction of cytology into clinical practice by Papanicolaou and Traut in 1944, it has become possible to detect cervical cancer in its preinvasive stages, thus reducing the morbidity and mortality from this disease.

The present study was conducted on 450 patients with the clinical diagnosis of unhealthy cervix.

Evaluation of maser results of our patients revealed that ASCUS, LGSIL, HGSIL, AGUS, Epidermoid carcinoma ratios were 6.4%, 3.8%, 1.6%, 0.2% and 0.% respectively (Table 3). According to abnormal colposcopy findings, abnormal colposcopy finding was found in 97 patients (21.6%). Of these patients, 18.5% had atypical vascularization, 16.4% had acetowhite epithelium + punctuation, 14.4+ had atypical vascularization + punctuation, 10.3% had atypical vascularization + acetowhite epithelium, 10.3% had punctuation, 5.1% had acetowhite epithelium + punctuation + mosaicism, 4.1% had acetowhite epithelium + punctuation + mosaicism + atypical vascularization. The correlation between abnormal cytology and histopathology was statistically significant (r=0.273, p=0.000 p<0.05) (Table 5). A statistically significant correlation was found between abnormal colposcopy finding and histopathology (r=0.613, p=0.002, p<0.05).

Table 5.

Correlation of abnormal cytology and colposcopy with histopatholgy.

Correlation Total patients (n) r p
Between abnormal cytology and histopathology 450 0.273 0.000
Between abnormal colposcopy and histopathology 450 0.613 0.002

Sensitivity, specificity, PPD and NPD of smear were found to be 0.57%, 0.76%,0.26% and 0.92% respectively in Table 6. On the other hand sensitivity, specificity, PPD and NPD of colposcopy were found to be 0.92%,0.67%, 0.52%,0.96% respectively.

Table 6.

Evaluation of negative predictive value, positive value, sensitivity and specificity of smear and colposcopy.

Method NPD (%) PPD (%) Sensitivity (%) Specificity (%)
Pap smear 0.92 0.26 0.57 0.76
Colposcopy 0.96 0.52 0.92 0.67

ASCUS is the most common and most controversial abnormal smear result (together with LSIL) about management. Therefore, there is a large body of research on ASCUS and LSIL patients. The most important and most comprehensive study is the randomized ALTS study which was mentioned earlier. That study aimed to determine the more correct management and follow-up mode of ASCUS and LSIL results. ASCUS and LSIL patients who were included in the study were randomly divided into cytological follow-up, immediate colposcopy and HPV groups. Sensitivities of ALTS study for these three methods are presented in HPV section. The results of the study revealed that the patients should be evaluated for all three methods for ASCUS and that HPV test should be preferred if liquid based cytology is used. As for LSIL patients, colposcopy was recommended due to high HPV (+). In ALTS study, for cytological follow-up group, it was reported that it was the most commonly used method, it had an error rate (–) of 20–50% for CIN 1 and that the rate of identifying CIN2/3 with a single cytology repeat was 67–85%. Major disadvantages in cytologic follow-up were reported to be CIN2/3, potential delay for cancer diagnosis, necessity of multiple repetitions, maladjustment and anxiety in the patient. Immediate colposcopy is advantageous as it allows for rapid diagnosis and can prevent potential losses. However, it is also considered as disadvantageous due to discomfort, causing unnecessary anxiety, high cost and possibility to cause excessive diagnosis and treatment. In immediate colposcopy group in ALTS study, although CIN3 lesion was 100% diagnosed, due to the fact that colposcopy costs 3–4 times higher than HPV test in the US, it is considered as a very expensive test. The ASCUS LSIL Triage Study (ALTS) Group, a large, randomized, multicenter trial designed to compare management strategies for women with ASCUS or LSIL cytology results, obtained the following data published in 2001: colposcopic findings for CIN I lesions were found in 51.4% of cases, and only 7% of examinations were considered to be CIN II or more severe. Among participants, the underlying prevalence of histologically confirmed CINIII was 5.1%. Compare to this data, in our study we found colposcopic findings for CIN I lesion in 78.5% of cases, 10.7% of examinations were CIN II or more severe. Among LSIL participants, the underlying prevalence of histologically confirmed CIN III was 3.5%. The data obtain from our study are appropriate as value noting that in ALTS study values were lower because directed biopsy was performed if any CIN lesion was suspected by colposcopic examination, so a lower number of biopsies reported to a lower number of colposcopies [10].

ASCUS rate of our study was 6.4% which depicts that the standardized diagnostic criteria for cervical cytological reporting were used by cytopathologist, so that the rate of atypical squamous cells (ASC) was between 3 to 5% of cytological diagnosis for accurate reporting as reported by Kurman et al. [11].

In our study, 5 of 28 patients who had ASCUS abnormal smear result and abnormal findings in colposcopy underwent LEEP+ECC. Histopathologies of 4 patients were reported to be chronic cervicitis, while 1 patient was koilocytic changes. 4 patients underwent conization. The results of 4 patients were reported as chronic cervicitis. 5 patients underwent colposcopy-directed biopsy and all patients were found to have cervicitis. Normal colposcopic findings were monitored in 14 patients with ASCUS abnormal smear result. The patients were followed up for smear. None of 28 ASCUS patients in abnormal smear result in Table 7 were found to have CIN or cervical carcinoma. Of 16 patients with LGSIL Pap test results, 2 were found to have CIN, while 1 was found to have HPV lesion with koilocytic changes and 2 were found to have LGSIL.

Table 7.

Evaluation of histopathology results of the patients with abnormal pap smear.

Smear results Results of histopathology N %
AGUS (n=1) Chronic cervitis 1 100.0
ASCUS (n=28) Normal 13 0.46
Chronic cervitis 13 0.46
Koilocytes changes 2 0.071
LGSIL (n=16) Normal 4 0.25
Chronic cervitis 7 0.43
LGSIL 2 0.125
Koilocytes changes 1 0.062
CIN 2 0.125
HGSIL (n=7) Normal 1 0.142
Chronic cervitis 6 0.85
CIS 1 0.142
Atypical cells (n=2) Chronic cervitis 1 0.5
Endometrium adeno cancer 1 0.5

Of 7 patients with HGSIL Pap test result, 1 had cervical carcinoma in situ. We believe that in patients with ASCUS smear result follow-up; and in patients with LGSIL and HGSIL result, histopathologic analysis is cost-effective.

1 patient who had atypical cell in abnormal smear result underwent colposcopy-directed biopsy. The result was reported as chronic cervicitis. On the other hand, further examination showed endometrium adenocarcinoma in 1 patient. In a similar study, Fallani et al. compared biopsy histologies of patients with ASCUS and SIL cytological diagnosis under colposcopy. A total of 358 of 584 women were diagnosed with LSIL. Biopsy of ASCUS patients showed CIN I in 36.3%; CIN II-III and in situ Ca in 15.7% and invasive Ca in 1 patient. The researchers found CIN I in 67.7%, CIN II-II and in situ Ca in 20.8% and Invasive Ca in 2 patients who had LSIL. Based on the results of the study, the researchers recommended colposcopic analysis for all patients with ASCUS and LSIL diagnosis [12].

In a study carried out on 118 patients who were diagnosed with HPV infected CIN, Gonzalez et al., analyzed the relationship between Bethesda system and colposcopic punch biopsy. They found 100% fit for HPV and 97% fit for CIN 1 in 82 (98.5%) LGSIL patients. They reported 84% fit for CIN II and 100% fit for CIN III in 36 (92%) HGSIL patients. The correlation was found to be 96% for PPD and 98% for NPD [13].

Women with clinical diagnosis of unhealthy cervix need cervical evaluation to detect any premalignant or malignant lesions of cervix. The Bethesda system used for cervical cytology is not only a uniform and standard method but also gives descriptive diagnosis that helps the gynecologist in individualized patient management. Communication between gynecologist and cytopathologist is required for best results of the cervical cytology reporting.

In our study, of 97 patients (21.6%) with abnormal colposcopic findings, 76 patients (16.9%) were diagnosed as ectropion, 45 patients (10%) were diagnosed as chronic cervicitis and 6 patients (1.3%) were diagnosed as cervical Tm.

Adams AL et al. noticed in their study that the true sensitivity of the whole diagnostic process of colposcopy plus biopsy is lower because biopsies were not performed for all women, and some of the biopsy specimens may not have been taken from the most severe lesion. This results in an overestimate of sensitivity [14].

Pimple SA et al., in 2010, made an evaluation of colposcopy vs. cytology as secondary test to triage women found positive on visual inspection test. The colposcopic impression was CIN I changes in 33.8% of cases, CIN II–III in 8.6% of cases, and invasive carcinoma in 2.7% of cases. Histopathology findings were reported as benign in 81.6%, CIN I in 5.8% of cases, CIN II in 2.9% of cases, CIN III in 2.6% of cases, and invasive carcinoma in 2.9% of cases. The estimates of sensitivity for low- and high-threshold colposcopy were 58% and 74.5%, respectively, and those of specificity were 57.5% and 92.9%, respectively [15].

Colposcopy performs better in differentiation of high-grade from low-grade disease than in differentiation of low-grade disease from normal cervix[16], and correlated with directed biopsy is described as the reference investigation or ‘gold standard’ for the diagnosis of cervical precancer [17].

Maziah AM et al., in 1991, in a comparative study of cytologic and colposcopic findings in preclinical cervical cancer, obtained an accuracy rate of 94% for colposcopy. The colposcopic findings rates were: 10% for CIN I, 34% for CIN II, 34% for CIN III and 12% for invasive carcinoma. Histology findings were: 10% were CIN I, 20% were CIN II, 60% were CIN III and 10% were micro-invasive carcinoma. In this study, the overall results were similar to ours, except that the diagnosis of micro-invasive carcinoma was not made on colposcopy. According to authors, poor results obtained were very likely because specific diagnosis in these techniques is very highly operator dependent and subjective and therefore a tendency to under diagnose the severity of lesions [17].

We found a statistically significant correlation between abnormal cytology and histopathology in Table 5 (r=0.273, p=0.000 p<0.05). The correlation between abnormal colposcopy finding and histopathology was statistically significant (r=0.613, p=0.002, p<0.05).

Sensitivity, specificity, PPD and NPD of smear were found to be 0.57%, 0.76%, 0.26% and 0.92% respectively in Table 6. Sensitivity, specificity, PPD and NPD of colposcopy were found to be 0.92%, 0.67%, 0.52% and 0.96% respectively.

The fact that all cervical examinations, smear collection and colposcopic evaluation were performed by a single gynecologist, that this physician received colposcopy training, similarly, only a single pathologist was included in the study and that the pathologist worked only in the field of gynecology eliminate intra-observer difference.

The significance of the study is that this is the first study carried out in a developing southeastern Anatolia region of Turkey on patients with low socio-economic status. The limitation of the study includes relatively low number of patients, high number of patients who were evaluated as normal in colposcopy and low number of cervical tumor patients. HPV DNA was not studied due to the fact that HPV DNA was not covered by insurance institutions in Turkey in the study period and that it was not routinely used due to its high cost. In their study, Olaniyan OB et al., in 2002 conducted a metaanalysis to quantify the validity of colposcopy in the diagnosis of early cervical neoplasia. Eight longitudinal studies were selected, which compared correlation of colposcopic impression with colposcopically directed biopsy results. The prevalence of cervical disease in the studies ranged from 40 to 89%. Colposcopic accuracy was 89%, which agreed exactly with histology in 61% of cases. The sensitivity and specificity of colposcopy for the threshold of normal vs. all cervical abnormalities were 87–99% and 26–87% respectively. For the threshold of normal and low-grade SIL vs. high-grade SIL, the values were 30–90% and 67–97% [19].

In a study meant to track the management outcomes of abnormal cervical cytology and hence confer credence to the value of colposcopy in management of abnormal cervical cytology, published in 2007, colposcopic detection rates were: 68% for CIN I, 73.3% for CIN II, 81.4% for CIN III and 88.9% for invasive carcinoma [20]. When deciding which test to use for screening, specificity must be taken into account because tests with low specificity applied to a healthy population with a very low prevalence of disease will result in a high proportion of false-positive test results [21]. Moss EL et al., in 2009, in a study on 469 patients to determine whether colposcopy is reliable in diagnosing cervical intraepithelial neoplasia in women who have undergone a previous cervical excision biopsy, reported the sensitivity and specificity of colposcopy for any cervical disease were 93.9% and 51.9%, respectively [22].

Conclusions

This study demonstrated high accuracy and correlation between colposcopy and histology, comparable with results from similar studies in the literature. Women with clinical diagnosis of unhealthy cervix should be evaluated by cytology to detect any premalignant or malignant lesions. It was concluded that Pap smear, colposcopy, and histopathology should be collectively evaluated in regions with low socio-economic status in evaluation of abnormal cervical findings.

Footnotes

Source of support: Departmental sources

References

  • 1.Ferlay J, Bray F, Pisani P, Parkin DM. Version 1.0 IARC Cancer Base No. 5. lyion: IARC Press; 2010. GLOBOCAN 2000: Cancer incidence, mortality and prevalence worldwide. 2001. [Google Scholar]
  • 2.Alphs HH, Wu TC, Roden RBS. Prevention and treatment of cervical cancer by vaccination. In: Bovicelli A, Giordano A, Kurman RJ, editors. Molecular pathology of gynecology cancer. Humana Press; Totowa, New Jersey: 2007. pp. 124–54. [Google Scholar]
  • 3.Ugboma HAA, Aburoma HLS. Pap smear: an important screening technique for preventing and detecting cervical cancer. Continental Journal of Medical Research. 2010;4:13–17. [Google Scholar]
  • 4.Shafi MI. Premalignant and malignant lesions of the cervix. In: Edmonds DK, editor. Dewhurst’s Textbook of Obstetrics and Gynaecology. 7th ed. Oxford, UK: Blackwell Publishing; 2007. [Google Scholar]
  • 5.Massad LS, Einstein MH, Huh WK, et al. 2012 Updated consensus guidelines for the management of abnormal cervical cancer screening tests and cancer precursors. Obstet Gynecol. 2013;121:829–46. doi: 10.1097/AOG.0b013e3182883a34. [DOI] [PubMed] [Google Scholar]
  • 6.Richart RM. A modified terminology for cervical intraepithelial neoplasia. Clin Obstet Gynecol. 1990;75(1):131–33. [PubMed] [Google Scholar]
  • 7.Verhoef VM, Heideman DA, van Kemenade FJ, et al. Methylation marker analysis and HPV16/18 genotyping in high-risk HPV positive self-sampled specimens to identify women with high grade CIN or cervical cancer. Gynecol Oncol. 2014;135(1):58–63. doi: 10.1016/j.ygyno.2014.08.003. [DOI] [PubMed] [Google Scholar]
  • 8.Solomon D, Davey DD, Kurman R, et al. The 2001 Bethesda System Terminology for reporting result of cervical cytology. JAMA. 2002;287:2114–19. doi: 10.1001/jama.287.16.2114. [DOI] [PubMed] [Google Scholar]
  • 9.Gamble M. Theory and practice of histological techniques. In: Bancroft JD, Gamble M, editors. The hematoxylins and eosin. 6th ed. Churchill Livingstone; 2008. pp. 121–34. [Google Scholar]
  • 10.Solomon D, Schiffman M, Tarone R ALTS Study Group. Comparison of three management strategies for patients with atypical squamous cells of undetermined significance: baseline results from a randomized trial. J Natl Cancer Inst. 2001;93(4):293–99. doi: 10.1093/jnci/93.4.293. [DOI] [PubMed] [Google Scholar]
  • 11.Kurman RJ, Henson DE, Herbst AL, et al. Interim guidelines for management of abnormal cervical cytology. The 1992 National Cancer Institute Workshop. JAMA. 1994;271:1866–69. [PubMed] [Google Scholar]
  • 12.Fallani MG, Pena C, Fambrini M, Marchionni M. [Cervical cytologic reports of ASCUS and LSIL. Cyto-histological correlation and implication for management]. Minerva Ginecol. 2002;54(3):263–69. [in Italian] [PubMed] [Google Scholar]
  • 13.Gonzalez Sanchez JL, Perez Guerrero C, Celorio Aguilera G, et al. [Cytologic correlation between the Bethesda system and colposcopic biopsy]. Ginecol Obstet Mex. 1998;66:330–34. [in Spanish] [PubMed] [Google Scholar]
  • 14.Adams AL, Eltoum I, Roberson J, et al. Negative colposcopic biopsy after positive human papilloma virus (HPV) DNA testing: false-positive HPV results or false-negative histologic findings? Am J Clin Pathol. 2006;125(3):413–18. [PubMed] [Google Scholar]
  • 15.Pimple SA, Amin G, Goswami S, Shastri SS. Evaluation of colposcopy vs. cytology as secondary test to triage women found positive on visual inspection test. Indian J Cancer. 2010;47(3):308–13. doi: 10.4103/0019-509X.64726. [DOI] [PubMed] [Google Scholar]
  • 16.Boonlikit S”. Correlation between Reid’s colposcopic index and histologic results from colposcopically directed biopsy in differentiating high-grade from low-grade squamous intraepithelial lesion at Rajavithi Hospital. Med Assoc Thai. 2011;94(Suppl 2):S59–65. [PubMed] [Google Scholar]
  • 17.Singer A, Monaghan JM, Quek SC, Deery ARS. Lower genital precancer: colposcopy, pathology and treatment. 2nd edition. Blackwell Science; 2000. [Google Scholar]
  • 18.Maziah AM, Sharifah NA, Yahya A. Comparative study of cytologic and colposcopic findings in preclinical cervical cancer. Malays J Pathol. 1991;13(2):105–8. [PubMed] [Google Scholar]
  • 19.Olaniyan OB. Validity of colposcopy in the diagnosis of early cervical neoplasia – a review. Afr J Reprod Health. 2002;6(3):59–69. [PubMed] [Google Scholar]
  • 20.Koigi-Kamau R, Kabare LW, Machoki JM. Impact of colposcopy on management outcomes of patients with abnormal cervical cytology. East Afr Med J. 2007;84(3):110–16. doi: 10.4314/eamj.v84i3.9512. [DOI] [PubMed] [Google Scholar]
  • 21.Dalla Palma P, Giorgi Rossi P, Collina G, et al. NTCC Pathology Group. The risk of false-positive histology according to the reason for colposcopy referral in cervical cancer screening: a blind revision of all histologic lesions found in the NTCC trial. Am J Clin Pathol. 2008;129(1):75–80. doi: 10.1309/EWYGWFRRM8798U5P. [DOI] [PubMed] [Google Scholar]
  • 22.Moss EL, Dhar KK, Byrom J, et al. The diagnostic accuracy of colposcopy in previously treated cervical intraepithelial neoplasia. J Low Genit Tract Dis. 2009;13(1):5–9. doi: 10.1097/LGT.0b013e31817f36d4. [DOI] [PubMed] [Google Scholar]

Articles from Medical Science Monitor : International Medical Journal of Experimental and Clinical Research are provided here courtesy of International Scientific Information, Inc.

RESOURCES