Cervical Dysplasia

Cervical dysplasia is a condition characterized by the presence of abnormal cells in the cervix, indicating either precancerous or cancerous cells. The condition is classified as low-grade or high-grade, depending on the extent of the abnormal cell growth. Low-grade cervical dysplasia progresses very slowly and typically resolves on its own. High-grade cervical dysplasia, however, tends to progress quickly and usually leads to cervical cancer. An estimated 66% of cervical dysplasia cases are estimated to progress to cancer within 10 years.

Signs and Symptoms

Cervical dysplasia often produces no symptoms and is usually discovered during an annual Pap smear.

Occasional signs and symptoms of the condition can include: It is important to note that these symptoms are not unique to cervical dysplasia and they may indicate a different problem. If you are experiencing any of these signs or symptoms, you should see your physician for an accurate diagnosis.

Causes

The precise cause of cervical dysplasia is not known. Studies have found a strong association between cervical dysplasia and infection with human papilloma virus (HPV), but additional factors (still unknown) must also be at play in order for cervical cells to change and become precancerous.

The following may increase your risk for cervical dysplasia:

Risk Factors

The following may increase an individual's risk for developing cervical dysplasia:

Diagnosis

If any of the symptoms mentioned earlier are present, the physician will perform a physical including an abdominal, back, and pelvic examination. As part of the pelvic exam, a Pap smear will be performed to detect precancerous or cancerous cells in the cervix. A Pap smear is also performed annually for screening purposes even when no symptoms are present. This test may be performed more or less often than once a year, depending on your individual medical history and risk factors for cervical cancer. For example, an individual who has had abnormal Pap smears in the past may require more tests than an individual who has always had normal Pap smears. But, if you have had normal pap smears 3 years in a row and you are over age 30, your doctor may perform a pap smear test only every 2 to 3 years. If there are any questionable or unclear results from the Pap smear, one of the following tests will be performed by a gynecologist:

Preventive Care

While there is no established strategy for preventing cervical dysplasia, regular Pap smears are the most effective and reliable method of identifying the condition in its early stages. Such early detection is key to preventing the condition from progressing to cervical cancer. Women should begin receiving annual Pap smears as soon as they become sexually active or no later than age 21. Women whose mothers took DES during pregnancy are advised to begin regular Pap smears at age 14, at the onset of their first menstrual period, or as soon as they become sexually active, whichever comes first.

Barrier contraceptives, such as condoms, may offer some degree of protection from cervical dysplasia.

Some lifestyle modifications may also help prevent the development of cervical dysplasia:

Treatment Approach

Surgical removal of abnormal tissue is the treatment of choice for cervical dysplasia. Medications are not used to treat cervical dysplasia, and few complementary or alternative therapies have been evaluated for their effectiveness in treating the condition. Several studies indicate, however, that the development and progression of cervical dysplasia may be related to certain nutritional deficiencies, including folate, beta-carotene, and vitamin C.

Medications

Medications are not used to treat cervical dysplasia.

Surgery and Other Procedures

Surgical removal of abnormal tissue is the most common method of treating cervical dysplasia. Ninety percent of these procedures can be done in an outpatient setting. These procedures include:

Nutrition and Dietary Supplements

Several population-based studies have suggested that eating a diet rich in the following nutrients from fruits and vegetables may protect against the development of cervical cancer:

Beta-carotene
Some research suggests that individuals deficient in beta-carotene may be more likely to develop cancerous or precancerous cervical lesions, but this relationship remains inconclusive. Other studies indicate that oral supplementation with beta-carotene may promote a regression, or decline in the signs of cervical dysplasia. Despite these promising results, the benefit of using beta-carotene supplements to prevent the development of cervical dysplasia or cervical cancer has not been proven.

Folate (Vitamin B9)

Like beta-carotene, some evidence suggests that folate (also known as vitamin B9) deficiencies may contribute to the development of cancerous or precancerous lesions in the cervix. Researchers also theorize that folate consumed in the diet may improve the cellular changes seen in cervical dysplasia by lowering homocysteine (a substance believed to contribute to the severity of cervical dysplasia) levels. The benefit of using dietary folate to prevent or treat cervical dysplasia has not been sufficiently proven.

Other dietary nutrients that may protect against the development of cervical cancer include: In addition, some of the risk factors for cervical dysplasia may cause certain nutritional deficiencies. For example, smoking may contribute to a deficiency in vitamin C and long-term use of birth control pills may diminish folate levels. Research has yet to prove whether taking vitamin C and folate supplements can help prevent or treat cervical dysplasia or cervical cancer. At the same time, it seems prudent to eat a diet rich in fruits and vegetables which contain vitamin C, folate, and beta-carotene, as these nutrients have been shown to have many health benefits.

Other Considerations

Pregnancy

Prognosis and Complications

Pap smears are essential to detecting precancerous lesions as well as early stages of cervical cancer. The regular use of Pap smears as a screening test has prevented millions of cases of cervical cancer and has saved a similar number of lives. Despite their value, they are not always 100% accurate. Up to 2% of women with normal Pap smear results actually have high-grade cervical dysplasia at the time of evaluation. In some rare cases, Pap smears may produce "false positive" results, meaning that a healthy woman may be falsely diagnosed with cervical dysplasia. Despite these errors, Pap smears are the most effective and reliable method of identifying cervical dysplasia.

Cervical cancer, a major complication of cervical dysplasia, is the leading cause of death in many developing and poorer countries and accounts for 4,800 deaths in the United States every year. Most cervical cancer deaths occur in women who have not had a Pap smear. Cervical cancer constitutes more than 10% of cancers worldwide and it is the second leading cause of death in women between the ages of 15 and 34.

With early identification, treatment, and consistent follow-up, nearly all cases of cervical dysplasia can be cured. Without treatment, many cervical dysplasia cases progress to cancer. Women who have been treated for cervical dysplasia have a lifetime risk for recurrence and malignancy. Fortunately, while the incidence of cervical dysplasia has been on the rise, the incidence of cervical cancer has declined dramatically. This may be due to improved screening techniques, which identify cases of cervical dysplasia in the early stages, before they have progressed to cancer.

References

Antony S, Kuttan R, Kuttan G. Effect of Viscum album in the inhibition of lung metatasis in mice induced by B16F10 melanoma cells. J Exp Clin Cancer Res. 1997;16(2):159-162.

Amitriptyline. NMIHI. Accessed at http://www.nmihi.com/a/amitriptyline.html on November 29, 2018.

Apgar BS, Brotzman G. HPV testing in the evaluation of the minimally abnormal Papanicolaou smear. Am Fam Physician. 1999;59(10):2794-2801.

Batieha AM, Armenian HK, Norkus EP, Morris JS, Spate VE, Comstock GW. Serum micronutrients and the subsequent risk of cervical cancer in a population-based nested case-control study. Cancer Epidemiol Biomarkers Prev. 1993;2(4):335-339.

Behrman RE, ed. Nelson Textbook of Pediatrics. 15th ed. Philadelphia,Pa: W.B. Saunders; 1996.

Brown AD, Garber AM. Cost-effectiveness of 3 methods to enhance the sensitivity of Papanicolaou testing. JAMA. 1999;281(4):347-353.

Butterworth CE Jr, Hatch KD, Macaluso M, et al. Folate deficiency and cervical dysplasia. JAMA. 1992(a);267(4):528-533.

Butterworth CE Jr, Hatch KD, Soong SJ, et al. Oral folic acid supplementation for cervical dysplasia: a clinical intervention trial. Am J Obstet Gynecol. 1992(b);166(3):803-809.

Canale ST. Campbell's Operative Orthopaedics. 9th ed. St. Louis, Mo: Mosby, Inc.; 1998.

Cervical Cancer. Patient Version. American Cancer Society. Accessed at https://www.cancer.org/ on November 29, 2018.

Cervical cancer. Office on Women's Health. Accessed at https://www.womenshealth.gov/ on November 29, 2018.

Cervical cancer. NMIHI. Accessed at http://www.nmihi.com/c/cervical-cancer.htm on November 29, 2018.

Childers JM, Chu J, Voigt LF, et al. Chemoprevention of cervical cancer with folic acid: a phase III Southwest Oncology Group Intergroup study. Cancer Epidemiol Biomarkers Prev. 1995;4(2):155-159.

Comerci JT Jr, Runowicz CD, Fields AL, et al. Induction of transforming growth factor-beta1 in cervical intraepithelial neoplasia in vivo after treatment with beta-carotene. Clin Cancer Res. 1997;3(2):157-160.

Cox JT. Evaluating the role of HPV testing for women with equivocal Papanicolaou test findings. JAMA. 1999;281(17):1645-1647.

Dambro MR, ed. Griffith's 5 Minute Clinical Consult. Baltimore, Md: Lippincott Williams & Wilkins, Inc.; 1999.

de Vet HC, Knipschild PG, Willebrand D, Schouten HJ, Sturmans F. The effect of beta-carotene on the regression and progression of cervical dysplasia: a clinical experiment. J Clin Epidemiol. 1991;44(3):273-283.

De Vita VT, Hellman S, Rosenberg SA, eds. Cancer: Principles and Practice of Oncology. 5th ed. Philadelphia, Pa: Lippincott-Raven Publishers; 1997.

Fairley CK, Tabrizi SN, Chen S, et al. A randomised clinical trial of beta-carotene vs placebo for the treatment of cervical HPV infection. Int J Gynecol Cancer. 1996;6:225-230.

Fauci AS, Braunwald E, Isselbacher KJ, et al, eds. Harrison's Principles of Internal Medicine. 14th ed. New York, NY: McGraw-Hill; 1998:609-610.

Fluconazole. NMIHI. Accessed at http://www.nmihi.com/f/fluconazole.html on November 29, 2018.

Giuliano AR, Gapstur S. Can cervical dysplasia and cancer be prevented with nutrients? Nutr Rev. 1998;56(1):9-16.

Goodman MT, McDuffie K, Hernandez B, Wilkens LR, Selhub J. Case-control study of plasma folate, homocysteine, vitamin B12, and cysteine as markers of cervical dysplasia. Cancer. 2000;89(2):376-382.

Hudson T. Cervical atypia, dysplasias and carcinoma in situ. Townsend Letter for Doctors and Patients. 1992;No. 102:32-41.

Kuttan G, Menon LG, Kuttan R. Prevention of 20-methylcholanthrene-induced sarcoma by a mistletoe extract, Iscador. Carcinogenesis. 1996;17(5):1107-1109.

Kwasniewska A, Tukendorf A, Semczuk M. Folate deficiency and cervical intraepithelial neoplasia. Eur J Gynaecol Oncol. 1997;18(6):526-530.

Lee KE, Koh CF, Watt WF. Comparison of the grade of CIN in colposcopically directed biopsies with that in outpatient loop electrosurgical excision procedure (LEEP) specimens—a retrospective review. Singapore Med J 1999;40(11):694-696.

Liao SY, Stanbridge EJ. Expression of MN/CA9 protein in Papanicolaou smears containing atypical glandular cells of undetermined significance is a diagnostic biomarker of cervical dysplasia and neoplasia. Cancer. 2000;88(5):1108-1121.

Liu T, Soong SJ, Alvarez RD, Butterworth CE Jr. A longitudinal analysis of human papillomavirus 16 infection, nutritional status, and cervical dysplasia progression. Cancer Epidemiol Biomarkers Prev. 1995;4(4):373-380.

Mackerras D, Irwig L, Simpson JM, et al. Randomized double-blind trial of beta-carotene and vitamin C in women with minor cervical abnormalities. Br J Cancer. 1999;79(9-10):1448-1453.

Manetta A, Schubbert T, Chapman J, et al. Beta-carotene treatment of cervical intraepithelial neoplasia: a phase II study. Cancer Epidemiol Biomarkers Prev. 1996;5(11):929-932.

Manos MM, Kinney WK, Hurley LB, et al. Identifying women with cervical neoplasia: using human papillomavirus DNA testing for equivocal Papanicolaou results. JAMA. 1999;281(17):1605-1610.

Margolis KL, Carson LF, Setness PA, et al. Are benign cellular changes on a Papanicolaou smear really benign? A prospective cohort study. Arch Fam Med. 1999;8(5):433-439.

Misoprostol. NMIHI. Accessed at http://www.nmihi.com/m/misoprostol.html on November 29, 2018.

Meyskens FL Jr, Manetta A. Prevention of cervical intraepithelial neoplasia and cervical cancer. Am J Clin Nutr. 1995;62(6 suppl):1417S-1419S.

Meyskens FL Jr, Surwit E, Moon TE, et al. Enhancement of regression of cervical intraepithelial neoplasia II (moderate dysplasia) with topically applied all-trans-retinoic acid: a randomized trial. J Natl Cancer Inst. 1994;86(7):539-543.

Murray MT, Pizzorno JE. Textbook of Natural Medicine. 2nd ed. London: Churchill Livingstone; 1999:1165-69, 1619-1620.

Muto Y, Fujii J, Shidoji Y, Moriwaki H, Kawaguchi T, Noda T. Growth retardation in human cervical dysplasia-derived cell lines by beta-carotene through down-regulation of epidermal growth factor receptor. Am J Clin Nutr. 1995;62(6 suppl):1535S-1540S.

Nagata C, Shimizu H, Higashiiwai H, et al. Serum retinol level and risk of subsequent cervical cancer in cases with cervical dysplasia. Cancer Invest. 1999;17(4):253-258.

Nagata C, Shimizu H, Yoshikawa H, et al. Serum carotenoids and vitamins and risk of cervical dysplasia from a case-control study in Japan. Br J Cancer. 1999;81(7):1234-1237.

National Cancer Institute. The 1988 Bethesda system for reporting cervical/vaginal cytological diagnoses. National Cancer Institute Workshop. JAMA. 1989;262(7):931.

Palan PR, Mikhail MS, Goldberg GL, Basu J, Runowicz CD, Romney SL. Plasma levels of beta-carotene, lycopene, canthaxanthin, retinol, and alpha- and tau-tocopherol in cervical intraepithelial neoplasia and cancer. Clin Cancer Res. 1996;2(1):181-185.

Peng YM, Peng YS, Childers JM, et al. Concentrations of carotenoids, tocopherols, and retinol in paired plasma and cervical tissue of patients with cervical cancer, precancer, and noncancerous diseases. Cancer Epidemiol Biomarkers Prev. 1998;7(4):347-350.

Perlman SE. Pap smears: screening, interpretation, treatment. Adolesc Med. 1999;10(2):243-254.

Pfenninger JL. Procedures for Primary Care Physicians. St. Louis, Mo: Mosby Year Book; 1994.

Richart RM, Jones HW III, Reid R. Classification and interpretation of Pap smears. Am Coll Obstet Gynecol Update. 1993;18(10):1-9.

Rock CL, Michael CW, Reynolds RK, Ruffin MT. Prevention of cervix cancer. Crit Rev Oncol Hematol. 2000;33(3):169-185.

Romney SL, Ho GY, Palan PR, et al. Effects of beta-carotene and other factors on outcome of cervical dysplasia and human papillomavirus infection. Gynecol Oncol. 1997;65(3):483-492.

Ryan KJ, ed. Kistner's Gynecology & Women's Health. 7th ed. St. Louis, Mo: Mosby, Inc.; 1999.

Saslow D, Runowicz CD, Solomon D, et al. American Cancer Society guideline for the early detection of cervical neoplasia and cancer. CA Cancer J Clin. 2002;52(6):342-362.

Schaefermeyer G, Schaefermeyer H. Treatment of pancreatic cancer with Viscum album (Iscador): a restrospective study of 292 patients 1986-1996. Complement Ther Med. 1998;6:172-177.

Sedjo RL, Inserra P, Abrahamsen M, et al. Human papillomavirus persistence and nutrients involved in the methylation pathway among a cohort of young women. Cancer Epidemiol Biomarkers Prev. 2002;11(4):353-359.

Symptoms of cervical cancer. American Academy of Family Physicians Accessed at https://familydoctor.org/ on November 29, 2018.

Sun XW, Kuhn L, Ellerbrock TV, Chiasson MA, Bush TJ, Wright TC Jr. Human papillomavirus infection in women infected with the human immunodeficiency virus. N Engl J Med. 1997;337(19):1343-1349.

Thomson SW, Heimburger DC, Cornwell PE, et al. Correlates of total plasma homocysteine: folic acid, copper, and cervical dysplasia. Nutrition. 2000;16(6):411-416.

Toba T, Shidoji Y, Fujii J, et al. Growth suppression and induction of heat-shock protein-70 by 9-cis beta-carotene in cervical dysplasia-derived cells. Life Sci. 1997;61(8):839-845.

VanEenwyk J, Davis FG, Bowen PE. Dietary and serum carotenoids and cervical intraepithelial neoplasia. Int J Cancer. 1991;48(1):34-38.

VanEenwyk J, Davis FG, Colman N. Folate, vitamin C, and cervical intraepithelial neoplasia. Cancer Epidemiol Biomarkers Prev. 1992;1(2):119-124.

What is cervical cancer? Ada Health. Accessed at https://ada.com/ on November 29, 2018.