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      High grade squamous intraepithelial lesion in inmates from Ohio: cervical screening and biopsy follow-up

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      CytoJournal
      BioMed Central

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          Abstract

          Background

          Cervical carcinoma remains the second leading cause of cancer death in women worldwide and sexual behavior is regarded as the main contributing factor. We studied cervical cytology screening with surgical biopsy follow-up in women prisoners and compared the findings to those in the general population.

          Methods

          We reviewed 1024 conventional cervical smears, 73 cervical biopsies and 2 loop electrosurgical excision procedure (LEEP) specimens referred to us from the Correctional Center in Columbus, Ohio during a 12-month period. The results were compared to 40,993 Pap smears from the general population for the same 12-month period.

          Results

          High grade squamous intraepithelial lesion (HGSIL) was diagnosed in 1.3% of the cervical smears from the inmate population versus 0.6% in the general population (p < 0.01). The unsatisfactory rate was 1.6% compared to 0.3% in the general population (p < 0.01). Among the study population, follow-up tissue diagnosis was obtained in 24.3% of the abnormal cytology results (ASCUS, LGSIL, and HGSIL). Of the HGSIL Pap smears, 61.5% had a subsequent tissue diagnosis. Thirty-nine biopsies (52% of the all inmate biopsies and LEEP) showed CIN II/III (cervical intraepithelial neoplasia II/III). Eight of these thirty-nine follow-up biopsies diagnosed as CIN II/III had a previous cervical cytology diagnosis of ASCUS. The average age for HGSIL was 30.5 years (S.D. = 5.7) and for low grade squamous intraepithelial lesion (LGSIL) was 27.2 years (S.D. = 6.1).

          Conclusion

          A significantly higher prevalence of HGSIL cervical cytology and unsatisfactory smears was encountered in female inmates, with tissue follow-up performed in less than two thirds of the patients with HGSIL. These results are in keeping with data available in the literature suggesting that the inmate population is high-risk and may be subject to less screening and tissue follow-up than the general population. Clinicians should proceed with urgency to improve screening and follow-up with treatment. The inmate population should be targeted for HPV vaccination promptly after FDA approval.

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          Most cited references17

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          The 1988 Bethesda System for reporting cervical/vaginal cytological diagnoses. National Cancer Institute Workshop.

          (1989)
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            Human papillomavirus, gonorrhea, syphilis, and cervical dysplasia in jailed women.

            We assessed the prevalence of human papillomavirus (HPV) by cervicovaginal lavage and Southern blot and inquired about behavioral risk factors for cervical disease and sexually transmitted diseases by interview in 114 female detainees at a large New York City jail. Of the women screened, 8% had abnormal Pap smears, 35% had HPV, 7% had gonorrhea, and 22% had serologic syphilis. Given the high rates of HPV infection and cervical cytology, Pap smears should be a routine intake procedure for incarcerated women.
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              Comprehensive cytopathology

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                Author and article information

                Journal
                Cytojournal
                CytoJournal
                BioMed Central (London )
                1742-6413
                2006
                10 May 2006
                : 3
                : 15
                Affiliations
                [1 ]Department of Pathology, Ohio State University, Memorial Hospital of Union County, 500 London Ave, Marysville, OH 43040, USA
                [2 ]Riverside Methodist Hospital, 3535 Olentangy River Road, Columbus, Ohio 43214, USA
                [3 ]Department of Pathology, Ohio State University Medical Center, N-339 Doan Hall, 410 West 10 th Avenue, Columbus, Ohio 43210-1218, USA
                Article
                1742-6413-3-15
                10.1186/1742-6413-3-15
                1475623
                16686955
                4b5e30cf-8319-40b3-ae9c-25b67b26bd06
                Copyright © 2006 Proca et al; licensee BioMed Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 25 January 2006
                : 10 May 2006
                Categories
                Research

                Clinical chemistry
                Clinical chemistry

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