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The prevalence of human papilloma virus DNA in women with mucopurulent endocervicitis
1Department of Microbiology and Clinical Microbiology, Turkey
2Department of Obstetrics and Gynecology, Ege University Faculty of Medicine, Izmir, Turkey
*Corresponding Author(s): I. Altuglu E-mail:
Objective: The aim of the study was to determine the prevalence of human papillomavirus (HPV) infection in a group of patients with mucopurulent endocervicitis.
Materials and methods: One hundred and forty-eight patients who came for their routine medical screening and were diagnosed with mucopurulent endocervicitis were enrolled in the study. HPV DNA was sought in cervical swab specimens placed in digene transport medium by use of the Digene Hybrid Capture assay.
Results: HPV infection was detected in 5.4% (8/148) of the patients with mucopurulent endocervicitis. The mean age of the patients was 36.4+/-8.2 (18-54) years. Approximately 40% (59/148) of the patients used intrauterine devices currently or in the past, while 16.2% (24/148) used combined oral contraceptives as the contraceptive method. HPV DNA was detected in eight patients: five had infections with low-risk subtypes, one with high/intermediate risk subtypes and one with the combination of high- and low-risk subtypes. The mean age of the HPV infected patients was significantly lower than the HPV negative patients (28.2+/-6.3 versus 36.9+/-8.1 years, p = 0.003). Risk factors for HPV infection did not differ between the infected and uninfected groups.
Conclusion: HPV infection should be sought in patients with clinical evidence of mucopurulent endocervicitis even without risk factors for cervical neoplasia.
HPV; Mucopurulent endocervicitis
I. Altuglu,M. C. Terek,T. Ozacar,A. A. Ozsaran,A. Bilgic. The prevalence of human papilloma virus DNA in women with mucopurulent endocervicitis. European Journal of Gynaecological Oncology. 2002. 23(2);166-168.
[1] Anon.: "Human papillomaviruses", vol 64. Lyon. International Agency for Research on Cancer, 1995.
[2] OzsaranA .A .,A te§ T.,D ikmen Y.,Z eytinoglu A.,T erek C.,E rhan Y., Ozacar T., Bilgic; A.: "Evaluation of the risk of cervical intraepithelial neoplasia and human papilloma virus infection in renal transplant patients receiving immunosuppressive therapy". Eur. J. Gynaecol. Oncol., 1999, 127.
[3] Walboomers J. M., Jacobs M. V., Manos M. M.: "Human papilloma Virus is a necessary cause of invasive cancer worldwide". J. Pathol.,1999,189,12.
[4] Herrington C. S.: "Do HPV-negative carcinomas exist?". J. Pathol., 1999, 189, I.
[5] Schiffman M. H., Brinton L.: "The epidemiology of cervical carcinogenesis". Cancer, 1995, 76, 1888.
[6] Tate J. E., Resnick M., Sheets E. E., Crum C. P.: "Absence of papillomavirus DNA in normal tissue adjacent to most cervical intraepithelial neoplasms". Obstet. Gynecol.; 1996, 88, 257.
[7] RemminkA. J., Walboomers J. M., HelmerhorstT. J. M., Voorhost F. J.,R ozendaal L., Risse E. K., Meijer C. J., Kenemans P.: "The presence of persistent high-risk HPV genotypes in dysplastic cervical lesions is associated with progressive disease: natural history up to 36 months". Int. J. Cancer., 1995, 61, 306.
[8] Vernon S. D., Unger E. R., Williams D.: "Comparison of human papillomavirus detection and typing by cycle sequencing, line blotting and hybrid capture". J. Clin. Microbial., 2000, 38, 651.
[9] Shah K. V.: "Papovaviruses", Specter S., Hodinka R. L., Young S. A. (eds.). In: "Clinical Virology Manual", 3''ed., Washington, ASM Press, 2000, 374.
[10] Davidson M., Schnitzer P. G., Bulkow L. R., Parkinson A. J., Schloss M. L., Fitzgerald M.A., et al.: "The prevalance of cervical infection with human papillomavirus and cervical dysplasia in Alaska N ative Woman". J. Inf Dis., 1994, 169, 792.
[11] Sendag F., Terek C., Tuncay G., Ozkinay E., Guven M.: "Single dose oral azithromycin versus seven day doxycycline in the treatment of non-gonococcal mucopurulent endocervicitis". Aust. N. Z. J. Obstet. Gynaecol., 2000, 40, 44.
[12] Bauer H. M., Ting Y., Greer C. E., Chambers J. C., Tashiro C. J., Chimera J., et al.: "Genital human papilloma virus infection in female university students as determined by a PCR-based method". JAMA, 1991, 265, 472.
[13] Lorincz A. T., Reid R., Jenson A. B., Greenberg M. D., Lancester W., Kurman R. J.: "Human papilloma virus infection of the cervix. Relative risk associations of 15 common anogenital types". Obstet. Gynecol., 1992, 79, 328.
[14] Woodman C. B. J., Collins S., Winter H., Bailey A., Ellis J., Prior P., et al.: "Natural history of cervical human papillomavirus infection in young women: a longitudinal cohort study". Lancet, 2001, 357, 1831.
[15] Trofatter K. F.: "Diagnosis of human papillomavirus genital tract infection". Am. J. Med., 1997, 102(5A), 21.
[16] Erensoy S., Erhan Y., Zeytinoglu A., Ozacar T.,Ozdemir N., Bilgic; A.: "DNA in situ hybridization in diagnosis of human papillomavirus infection". Clin. Diag. Viral., 1986, 5, 219.
[17] Bonnez W., Reichman R. C.: "Papillomaviruses". Mandell G. L., Bennett J. E., Dolin R. (eds.). In: "Mandell, Douglas and Bennett's Principles and Practice of Infectious Diseases", 5'h ed., Philadelfia Churchill Livingstone, 2000, 1630.
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