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Gynecologic Cryosurgery Treatment & Management

  • Author: E L Kristiina Parviainen, MD; Chief Editor: Michel E Rivlin, MD  more...
 
Updated: Jan 27, 2015
 

Preoperative Details

No special preparation is required by the patient or physician prior to cryosurgery. The patient should be informed of the potential risks, benefits, failure rates, and alternatives to the procedure.

Prior to performing the procedure, the practitioner should confirm that the patient is not pregnant and is free of vaginal and cervical infections. The practitioner should review the Pap test, colposcopy, and ECC results to confirm that the patient is an appropriate candidate for cryosurgery. The lesion should not extend into the endocervical canal because this reduces the likelihood of success for the procedure.[24, 25]

The equipment required to perform cervical cryosurgery is as follows:

  • Appropriately sized vaginal specula
  • Adequate light source
  • Refrigerant source - Liquid nitrous oxide
  • Cervical probes in a variety of sizes
  • Lubricant
  • Topical hemostatic agents

The following information may be provided to patients prior to their procedure.

Sample patient information sheet

Your doctor has determined that you have cervical dysplasia, which may be treated with cryosurgery. Cryosurgery is a procedure in which the abnormal cells on your cervix are destroyed by freezing. This procedure can be as much as 90% effective in eliminating the abnormal tissue. This procedure is performed in the office.

Prior to the procedure:

  • Notify your provider if you have (or will have) your period on the day of the procedure so it can be rescheduled when your period is over.
  • Notify your provider if you think that you might be pregnant. Cryosurgery usually is not performed during pregnancy because it might endanger the pregnancy.

Day of the procedure:

  • You may take a medication such as ibuprofen or acetaminophen 1-2 hours prior to your scheduled procedure.
  • No anesthetic is required for the procedure.
  • Your provider will perform the cryosurgery procedure in the office, which will require 15-20 minutes.
  • You may experience uterine cramping during and immediately after the procedure.

After the procedure:

  • You may return to work.
  • You may notice an abundant gray, white, or clear vaginal discharge for 2-4 weeks, which may have an odor. This is to be expected and is evidence of cells sloughing from the cervix.
  • Do not use tampons, douche, or have sexual intercourse for 4 weeks after treatment because this may result in infection or bleeding, which could delay the healing process.
  • You may take ibuprofen or acetaminophen for pain relief.
  • You may shower at any time after the treatment. Avoid tub baths until the vaginal discharge resolves.

Reasons to contact your provider:

  • Temperature above 38°C
  • Vaginal bleeding equal to or greater than a normal period
  • Pain not relieved by ibuprofen or acetaminophen
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Intraoperative Details

Technique

In order to achieve hypothermia, liquid refrigerants are forced through a small hole at a pressure range of 750-900 pounds per square inch (psi).[26] This produces a very low temperature at the surface of the probe due to the Joule-Thompson effect. The temperature at the probe tip can range from -65°C to -85°C. Cell death occurs secondary to crystallization of intracellular water at -20°C to -30°C.[27, 24, 25] Proposed mechanisms for cell destruction include dehydration, crystallization, denaturation of membrane proteins, thermal shock, and vascular stasis.[22]

The refrigerant most commonly used at present is liquid nitrous oxide (N2 O). It is available commercially and is relatively inexpensive. A 2008 study found N2 O to be superior to carbon dioxide cryotherapy as indicated by greater mean depth of tissue necrosis with N2 O.[28]

The external temperature of the probe depends on the conductivity of the probe material. Silver and copper are the best materials for use in probe tips because high conductivity produces both a better freezing effect and more effective local cryonecrosis.[22] Adequate cryonecrosis of the tissue depends on direct contact of the probe with the lesion. This is best achieved with a water-based lubricant coating an appropriately sized probe. Boonstra and others have shown that the size and shape of the probe can dramatically affect the depth of cryonecrosis.[24, 25] The cryotip should cover the entire lesion and transformation zone. The 19- and 25-mm mini-cone tips are recommended by Campion.

A double-freeze technique in which the tissue is frozen for a period of several minutes, thawed completely, and then refrozen is preferred to single freeze.[29] Creasman[30] demonstrated that this method was significantly more efficacious than a single-freeze method. The freeze-thaw-freeze is divided as follows:

  • Freeze for 3 minutes
  • Thaw for 5 minutes
  • Freeze for 3 minutes

The freeze time required depends largely on the ice ball that is generated on the cervix. Campion in the 2005 edition of Practical Gynecologic Oncology recommends that the ice ball extend 7 mm laterally beyond the edge of the probe in order to achieve a 5-mm depth of destruction.[27] This suggests that the operator need not watch the elapsed time, but rather monitor the width of the ice ball formed.

Procedure

This is carried out as follows:

  • The patient is carefully selected, as previously described
  • She is premedicated with nonsteroidal anti-inflammatory drugs (NSAIDs)
  • A speculum is placed in the vagina to adequately expose the cervix and prevent contact of the probe tip with the vaginal walls and speculum
  • Location and size of the lesion is confirmed by colposcopy or has previously been noted
  • A water-soluble gel is applied to the tip of an appropriately sized probe, which is positioned over the lesion and transformation zone
  • The flow of refrigerant is initiated, and the ice ball formation is observed carefully
  • Thawing and refreezing then are carried out, if the operator prefers

A literature review by Sauvaget et al indicated that cryotherapy is a safe and effective means of treating CIN, with the investigators finding cryotherapeutic cure rates for CIN1, CIN2, and CIN3 or 94%, 92%, and 85%, respectively. The study, which included 77 papers (28,827 total cases of treated CIN), found that cure rates were significantly increased when the double-freeze method was used and patients had no endocervical involvement.[31]

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Postoperative Details

Postprocedure symptoms include the following:

  • Cramping: This can be minimized with pretreatment NSAIDs. Mucosal and paracervical block typically are not used.
  • Hydrorrhea: Most authors describe 2-4 weeks of profuse watery discharge, which may be greater in obese women. Debridement of the cervical eschar 48 hours after the cryosurgical procedure does not ameliorate this symptom. [32]
  • Bleeding: This symptom is rare.
  • Infection: This is a rare complication. Prophylactic antibiotics are not indicated.

Cellular repair

  • Crisp reports that 60% of patients were found to have normal histology findings on cervical biopsy at 6 weeks and 90% by 10 weeks.
  • Cervical cytology is difficult to interpret during the first 6 weeks due to the healing process, but then it returns to normal.
  • The squamocolumnar junction recedes deeper into the endocervical canal after cryosurgery. [3]
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Follow-up

Acceptable strategies recommended by the ACOG Practice Bulletin on Management of Abnormal Cervical Cytology and Histology for follow-up after cryotherapy include (1) HPV testing at 6-12 months, (2) HPV & cytology at 6-month intervals, or (3) cytology alone at 6 month intervals.[5] Factors that may affect screening frequency include size and grade of the lesion and patient compliance.

For excellent patient education resources, visit eMedicineHealth's Cancer Center and Women's Health Center. Also, see eMedicineHealth's patient education articles Cervical Cancer and Pap Smear.

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Complications

Potential impact on fertility, scarring complicating follow-up, and carcinoma developing postcryosurgery are the main concerns.

  • Fertility: Theoretical concerns about reduced fertility include the induction of cervical stenosis, a detrimental effect on cervical mucus, cervical incompetence, and tubal dysfunction secondary to ascending infection. No conclusive clinical evidence supports any of these concerns. [33, 34, 35]
  • Scarring complicating follow-up colposcopy: Of particular concern is the receding of the squamocolumnar junction into the endocervical canal. [36, 37] In a series of 204 patients, post-treatment colposcopy was adequate in 50% of patients after cryosurgery and 79% of patients after laser surgery. [38] A more recent report of a small series of women treated with cryotherapy (n=82), LEEP (n=24), and no procedure (n=96), yielded likelihood odds ratios of 3.01 (0.78-11.58) for LEEP and 18.66 (6.99-49.81) for cryotherapy of inadequate follow-up colposcopic evaluation post procedure as compared with the no procedure group. [39]
  • Development of carcinoma postcryotherapy: In a series of invasive carcinoma diagnosed after cryotherapy, carcinoma was associated with the following findings: inappropriate evaluation prior to cryotherapy (57%), erroneous initial interpretation of ectocervical biopsies (20%), and erroneous initial interpretation of ECC specimens (67%). [40] Appropriate preoperative evaluation is the key to minimizing the risk of postcryosurgery carcinoma.
  • Anaphylactoid reaction has been reported as a reaction to the cold exposure. [41] Physicians performing cryosurgery should be aware of this potential risk and be familiar with its treatment.
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Outcome and Prognosis

Cryosurgery can be an effective treatment for premalignant squamous lesions of the uterine cervix.[42] Recurrence rates are low and depend, in part, on the size and grade of the lesion, as well as its location (ectocervix versus endocervix). Boonstra and colleagues examined hysterectomy specimens of women who received cryosurgery for CIN prior to hysterectomy. They reported that a success rate as high as 100% could be achieved using a large conical probe and an adequate freeze time based on the 64 patients they studied.[25]

Technical aspects that impact results include the method utilized, freeze and thaw time, size and extent of the ice ball that is formed, probe size and shape, and the refrigerant temperature.

Although many authors have investigated overall success rates, few have conducted large-scale prospective studies. Benedet and others reported on 1675 women with varying degrees of CIN and demonstrated an overall success rate of 94%.[43] Further work by this same group in 1990 demonstrated an 88% success rate in 962 women in a higher-risk group in which more than half of the patients had severe dysplasia or CIS. Gordon and Duncan presented data from 1628 patients with severe dysplasia and found an initial 93% success rate. This study followed patients' cases for as long as 6 years after the procedure, and, in this group, the long-term success rate was 91%.[44]

Assessment of the subset of patients with severe dysplasia (CIN 3) treated with cryosurgery has yielded disparate results from different authors, with failure rate ranges of 7.1-38.8%. Bryson reported an 11-year study of patients with biopsy-proven severe dysplasia or CIS and found a 7.1% failure rate.[45] Townsend and Ostergard followed the cases of 62 patients with severe dysplasia or CIS and found an 11.8% failure rate for those with severe dysplasia and 10% for those with CIS.[4] In a follow-up study, Ostergard reported a 7.1% failure rate in 28 patients with severe dysplasia and an alarming 38.8% failure rate in 18 patients with the diagnosis of CIS.[46] Failure rates for cryosurgical treatment have been reported to be consistently higher in patients with severe dysplasia and CIS than in patients with mild or moderate dysplasia.

Numerous investigators have compared the efficacy of cryosurgery and laser vaporization in the treatment of CIN. The two methods appear to be equally efficacious. Proponents of laser therapy stress the capacity to achieve precise destruction, and thereby more complete destruction, of the lesion by this method. Recurrence and persistence rates reported in the literature do not support this assertion. Laser equipment also is significantly more expensive than the cryoprobe apparatus, and patients report more pain during the laser vaporization. No proven benefit of laser therapy over cryosurgery exists.

A 2003 cost-effectiveness model on management of CIN 2/3 found cryotherapy, LEEP, and hysterectomy to be superior to observation, laser therapy, and cold knife cone.[47] LEEP was more effective than cryotherapy but also more expensive at a cost of $31,347 per CIN cure and $1.8 million per cancer prevented. Hysterectomy was the most effective and most expensive. Cryotherapy should continue to have a role in the treatment of cervical intraepithelial dysplasia, with increasing focus on resource utilization in our health care system.

Mitchel et al compared cryosurgery, laser vaporization, and LEEP finding no difference in success or complication rates. However, persistence was reported to be greater in patients with larger lesions, history of prior treatment, older women (>30 y), and those with HPV 16 or 18.[48, 49] Another randomized trial comparing LEEP with cryotherapy did demonstrate higher cure rate following LEEP at 12-month follow-up for women with high-grade lesions, but concluded that cryotherapy has an "acceptable" cure rate and hence remains a good option for low-resource countries.[50]

In a study by Singh et al, LEEP was associated with higher cure rates; however, the difference was not statistically significant. LEEP had a slightly better outcome than cryotherapy when used on severe lesions.[51]

The 2009 Cochrane review on surgery for CIN, concludes that while cryotherapy has equal efficacy to other modalities for the treatment of low-grade lesions, a trend toward greater residual disease following treatment of high-grade lesions with cryotherapy precludes recommending the use of cryotherapy for high-grade lesions.[29]

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Future and Controversies

Despite the 85-95% success rate reported in most series, practitioners continue to be concerned about the potential for persistent disease and missed diagnosis of invasive carcinoma. Several investigators have reported a disparity between colposcopic biopsies and cone biopsy specimens.[52] For this reason, LEEP, which provides tissue for pathologic diagnosis, has replaced cryosurgery in many cases in the ambulatory setting.

Several topical agents, including imiquimod, are currently being evaluated for efficacy in treatment of CIN. Future studies will no doubt determine their role in clinical practice.

Increasingly, physicians also are offering expectant management for patients with CIN 1 lesions and reserving therapy for CIN 2/CIN 3. Remember that eliminating HPV from the genital tract is not possible, and, therefore, women with a history of CIN remain at risk for recurrence.

Given the recent availability of the HPV vaccine, the prevalence and management of CIN may be dramatically altered in the decades to come.

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Contributor Information and Disclosures
Author

E L Kristiina Parviainen, MD Assistant Professor, Department of Obstetrics, Gynecology and Reproductive Sciences, Division of Maternal-Fetal Medicine, University of Pittsburgh School of Medicine

E L Kristiina Parviainen, MD is a member of the following medical societies: Alpha Omega Alpha, Association of Professors of Gynecology and Obstetrics, Society for Reproductive Investigation, Society for Maternal-Fetal Medicine, American College of Obstetricians and Gynecologists

Disclosure: Nothing to disclose.

Coauthor(s)

Nancy D Gaba, MD Associate Dean for Graduate Medical Education, Director of Obstetrics and Gynecology Residency Program, Director of Division of General Gynecology and Associate Professor, Department of Obstetrics and Gynecology, George Washington University School of Medicine

Nancy D Gaba, MD is a member of the following medical societies: American College of Obstetricians and Gynecologists, Association of Professors of Gynecology and Obstetrics, Medical Society of the District of Columbia

Disclosure: Nothing to disclose.

Chief Editor

Michel E Rivlin, MD Former Professor, Department of Obstetrics and Gynecology, University of Mississippi School of Medicine

Michel E Rivlin, MD is a member of the following medical societies: American College of Obstetricians and Gynecologists, American Medical Association, Mississippi State Medical Association, Royal College of Surgeons of Edinburgh, Royal College of Obstetricians and Gynaecologists

Disclosure: Nothing to disclose.

Acknowledgements

Francisco Talavera, PharmD, PhD Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Medscape Reference Salary Employment

References
  1. ACOG. ACOG Practice Bulletin number 109, December 2009. Cervical cytology screening. Obstet Gynecol. 2009 Dec. 114(6):1409-1420.

  2. Solomon D, Davey D, Kurman R, Moriarty A, O'Connor D, Prey M, et al. The 2001 Bethesda System: terminology for reporting results of cervical cytology. JAMA. 2002. 287:2114-9.

  3. Crisp WE, Smith MS, Asadourian LA. Cryosurgical treatment of premalignant disease of the uterine cervix. Am J Obstet Gynecol. 1970 Jul 1. 107(5):737-42. [Medline].

  4. Townsend DE, Ostergard DR. Cryocauterization for preinvasive cervical neoplasia. J Reprod Med. 1971 Apr. 6(4):171-6. [Medline].

  5. ACOG Practice Bulletin No. 99: management of abnormal cervical cytology and histology. Obstet Gynecol. 2008 Dec. 112(6):1419-44. [Medline].

  6. Ostor AG. Natural history of cervical intraepithelial neoplasia: a critical review. Int J Gynecol Pathol. 1993 Apr. 12(2):186-92. [Medline].

  7. Schlecht NF, Platt RW, Duarte-Franco E, Costa MC, Sobrinho JP, Prado JC. Human papillomavirus infection and time to progression and regression of cervical intraepithelial neoplasia. J Natl Cancer Inst. 2003 Sep 3. 95(17):1336-43. [Medline].

  8. Brown DR, Shew ML, Qadadri B, Neptune N, Vargas M, Tu W. A longitudinal study of genital human papillomavirus infection in a cohort of closely followed adolescent women. J Infect Dis. 2005 Jan 15. 191(2):182-92. [Medline].

  9. Moscicki AB, Shiboski S, Hills NK, Powell KJ, Jay N, Hanson EN. Regression of low-grade squamous intra-epithelial lesions in young women. Lancet. 2004 Nov 6-12. 364(9446):1678-83. [Medline].

  10. American Cancer Society. Cancer facts and figures 2009. American Cancer Society. Available at http://www.cancer.org/download/STT/500809. Accessed: 4/30/2010.

  11. Devesa SS. Descriptive epidemiology of cancer of the uterine cervix. Obstet Gynecol. 1984 May. 63(5):605-12.

  12. Schoell WM, Janicek MF, Mirhashemi R. Epidemiology and biology of cervical cancer. Semin Surg Oncol. 1999 Apr-May. 16(3):203-11. [Medline].

  13. Smith R. CA - A Cancer Journal for Clinicians. Philadelphia, Pa: Lippincott, Williams, & Wilkins; 2001. 51: 18-44.

  14. Cirisano FD. Management of pre-invasive disease of the cervix. Semin Surg Oncol. 1999 Apr-May. 16(3):222-7. [Medline].

  15. Insinga RP, Glass AG, Rush BB. Diagnoses and outcomes in cervical cancer screening: a population-based study. Am J Obstet Gynecol. 2004 Jul. 191(1):105-13. [Medline].

  16. CDC National Cancer Institute Factsheet. Human papillomavirus and cancer; Questions and answers. CDC. Available at www.cancer.gov/cancertopics/factsheet/Risk/HPV. Accessed: 4/30/2010.

  17. Richart RM. Natural history of cervical intraepithelial neoplasia. Clin Obstet Gynecol. 1968. 10:748-784.

  18. Fu YS, Reagan JW, Richart RM. Definition of precursors. Gynecol Oncol. 1981 Oct. 12(2 Pt 2):S220-31. [Medline].

  19. Hollingsworth RE, Lee WH. Tumor suppressor genes: new prospects for cancer research. J Natl Cancer Inst. 1991 Jan. 83(2):91-6.

  20. Lorincz AT, Reid R, Jenson AB. Human papillomavirus infection of the cervix: relative risk associations of 15 common anogenital types. Obstet Gynecol. 1992 Mar. 79(3):328-37.

  21. Willett GD, Kurman RJ, Reid R. Correlation of the histologic appearance of intraepithelial neoplasia of the cervix with human papillomavirus types. Emphasis on low grade lesions including so-called flat condyloma. Int J Gynecol Pathol. 1989. 8(1):18-25. [Medline].

  22. Charles EH, Savage EW, Hacker N. Cryosurgical treatment of cervical intraepithelial neoplasia. Gynecol Oncol. 1981 Aug. 12(1):83-8. [Medline].

  23. Precancerous Lesions of the Cervix. Kurman RJ. Blaustein's Pathology of the Female Genital Tract. 5th. New York: Springer-Verlag; 2002.

  24. Boonstra H, Aalders JG, Koudstaal J. Minimum extension and appropriate topographic position of tissue destruction for treatment of cervical intraepithelial neoplasia. Obstet Gynecol. 1990 Feb. 75(2):227-31. [Medline].

  25. Boonstra H, Koudstaal J, Oosterhuis JW. Analysis of cryolesions in the uterine cervix: application techniques, extension, and failures. Obstet Gynecol. 1990 Feb. 75(2):232-9. [Medline].

  26. Figge DC, Creasman WT. Cryotherapy in the treatment of cervical intraepithelial neoplasia. Obstet Gynecol. 1983 Sep. 62(3):353-8. [Medline].

  27. Campion Michael J. Preinvasive Disease. Jonathan S. Berek and Neville F. Hacker. Practical Gynecologic Oncology. 4th. Philadelphia, PA: Lippincott Williams & Wilkins; 2005. 265-309.

  28. Mariategui J, Santos C, Taxa L, Jeronimo J, Castle PE. Comparison of depth of necrosis achieved by CO2- and N2O-cryotherapy. Int J Gynaecol Obstet. 2008 Jan. 100(1):24-6. [Medline].

  29. Martin-Hirsch pp, Paraskevaidis E, Kitchener HC. Surgery for intraepithelial neoplasia. The Cochrane Collaboration. 2009:[Full Text].

  30. Creasman WT, Hinshaw WM, Clarke-Pearson DL. Cryosurgery in the management of cervical intraepithelial neoplasia. Obstet Gynecol. 1984 Feb. 63(2):145-9. [Medline].

  31. Sauvaget C, Muwonge R, Sankaranarayanan R. Meta-analysis of the effectiveness of cryotherapy in the treatment of cervical intraepithelial neoplasia. Int J Gynaecol Obstet. 2013 Mar. 120(3):218-23. [Medline].

  32. Harper DM, Mayeaux EJ Jr, Daaleman TP. The natural history of cervical cryosurgical healing. The minimal effect of debridement of the cervical eschar. J Fam Pract. 2000 Aug. 49(8):694-700. [Medline].

  33. Weed JC Jr, Curry SL, Duncan ID. Fertility after cryosurgery of the cervix. Obstet Gynecol. 1978 Aug. 52(2):245-6. [Medline].

  34. Hemmingsson E, Stendahl U, Stenson S. Cryosurgical treatment of cervical intraepithelial neoplasia with follow-up of five to eight years. Am J Obstet Gynecol. 1981 Jan 15. 139(2):144-7. [Medline].

  35. Montz FJ. Impact of therapy for cervical intraepithelial neoplasia on fertility. Am J Obstet Gynecol. 1996 Oct. 175(4 Pt 2):1129-36. [Medline].

  36. Ferenczy A. Comparison of cryo- and carbon dioxide laser therapy for cervical intraepithelial neoplasia. Obstet Gynecol. 1985 Dec. 66(6):793-8. [Medline].

  37. Johnson VW, Homesley HD. Comparison of cryosurgery and carbon dioxide laser ablation for treatment of cervical intraepithelial neoplasia. Colposc Gynecol Laser Surg. 1984. 173-180.

  38. Berget A, Andreasson B, Bock JE. Laser and cryo surgery for cervical intraepithelial neoplasia. A randomized trial with longterm follow-up. Acta Obstet Gynecol Scand. 1991. 70(3):231-5. [Medline].

  39. Sparks RA, Scheid D, Loemker V, et al. Association of cervical cryotherapy with inadequate follow-up colposcopy. J Fam Pract. 2002 Jun. 51(6):526-9. [Medline].

  40. Schmidt C, Pretorius RG, Bonin M. Invasive cervical cancer following cryotherapy for cervical intraepithelial neoplasia or human papillomavirus infection. Obstet Gynecol. 1992 Nov. 80(5):797-800. [Medline].

  41. Ben-Arie A, Kogan S, Fink A. Anaphylactoid reaction after cryotherapy of the cervix. Obstet Gynecol. 1999 May. 93(5 Pt 2):841. [Medline].

  42. Wojciech R. The importance of cryosurgery in gynecological practice. Ginekol Pol. 2011 Aug. 82(8):618-22. [Medline].

  43. Benedet JL, Miller DM, Nickerson KG. The results of cryosurgical treatment of cervical intraepithelial neoplasia at one, five, and ten years. Am J Obstet Gynecol. 1987 Aug. 157(2):268-73. [Medline].

  44. Gordon HK, Duncan ID. Effective destruction of cervical intraepithelial neoplasia (CIN) 3 at 100 degrees C using the Semm cold coagulator: 14 years experience. Br J Obstet Gynaecol. 1991 Jan. 98(1):14-20. [Medline].

  45. Bryson SC, Lenehan P, Lickrish GM. The treatment of grade 3 cervical intraepithelial neoplasia with cryotherapy: an 11-year experience. Am J Obstet Gynecol. 1985 Jan 15. 151(2):201-6. [Medline].

  46. Ostergard DR. Cryosurgical treatment of cervical intraepithelial neoplasia. Obstet Gynecol. 1980 Aug. 56(2):231-3. [Medline].

  47. Kleinberg MJ, Straughn JM, Stringer JS, Partridge EE. A cost-effectiveness analysis of management strategies for cervical intraepithelial neoplasia grades 2 and 3. Am J Obstet Gynecol. 2003 May. 188(5):1186-8. [Medline].

  48. Mitchell MF, Tortolero-Luna G, Cook E. A randomized clinical trial of cryotherapy, laser vaporization, and loop electrosurgical excision for treatment of squamous intraepithelial lesions of the cervix. Obstet Gynecol. 1998 Nov. 92(5):737-44. [Medline].

  49. Nuovo J, Melnikow J, Willan AR. Treatment outcomes for squamous intraepithelial lesions. Int J Gynaecol Obstet. 2000 Jan. 68(1):25-33. [Medline].

  50. Chirenje ZM, Rusakaniko S, Akino V, Mlingo M. A randomised clinical trial of loop electrosurgical excision procedure (LEEP) versus cryotherapy in the treatment of cervical intraepithelial neoplasia. J Obstet Gynaecol. 2001 Nov. 21(6):617-21. [Medline].

  51. Singh A, Arthur B, Agarwal V. LEEP Verses Cryotherapy in CIN. J Obstet Gynaecol India. 2011 Aug. 61(4):431-5. [Medline]. [Full Text].

  52. Skehan M, Soutter WP, Lim K. Reliability of colposcopy and directed punch biopsy. Br J Obstet Gynaecol. 1990 Sep. 97(9):811-6. [Medline].

  53. Andersen ES, Thorup K, Larsen G. The results of cryosurgery for cervical intraepithelial neoplasia. Gynecol Oncol. 1988 May. 30(1):21-5. [Medline].

  54. Barron BA, Richart RN. A statistical model of the natural history of cervical carcinoma based on a prospective study of 557 cases. J. Nat Cancer Inst. 1968. 41:1343-53.

  55. Benedet JL, Miller DM, Nickerson KG. Results of conservative management of cervical intraepithelial neoplasia. Obstet Gynecol. 1992 Jan. 79(1):105-10. [Medline].

  56. Benedet JL, Nickerson KG, Anderson GH. Cryotherapy in the treatment of cervical intraepithelial neoplasia. Obstet Gynecol. 1981 Dec. 58(6):725-9. [Medline].

  57. Berget A, Andreasson B, Bock JE. Outpatient treatment of cervical intra-epithelial neoplasia. The CO2 laser versus cryotherapy, a randomized trial. Acta Obstet Gynecol Scand. 1987. 66(6):531-6. [Medline].

  58. Crisp WE. Cryosurgical treatment of neoplasia of the uterine cervix. Obstet Gynecol. 1972 Apr. 39(4):495-9. [Medline].

  59. Dunton CJ. Cryotherapy: evidence-based interventions and informed consent. J Fam Pract. 2000 Aug. 49(8):707-8. [Medline].

  60. Hatch KD, Shingleton HM, Austin JM Jr. Cryosurgery of cervical intraepithelial neoplasia. Obstet Gynecol. 1981 Jun. 57(6):692-8. [Medline].

  61. Kalliala I, Anttila A, Pukkala E, Nieminen P. Risk of cervical and other cancers after treatment of cervical intraepithelial neoplasia: retrospective cohort study. BMJ. 2005 Nov 19. 331(7526):1183-5. [Medline].

  62. Kalliala I, Nieminen P, Dyba T, Pukkala E, Anttila A. Cancer free survival after CIN treatment: comparisons of treatment methods and histology. Gynecol Oncol. 2007 Apr. 105(1):228-33. [Medline].

  63. Kaufman RH, Irwin JF. The cryosurgical therapy of cervical intraepithelial neoplasia. III. Continuing follow-up. Am J Obstet Gynecol. 1978 Jun 15. 131(4):381-8. [Medline].

  64. Kirwan PH, Smith IR, Naftalin NJ. A study of cryosurgery and the CO2 laser in treatment of carcinoma in situ (CIN III) of the uterine cervix. Gynecol Oncol. 1985 Oct. 22(2):195-200. [Medline].

  65. Koutsky LA, Holmes KK, Critchlow CW. A cohort study of the risk of cervical intraepithelial neoplasia grade 2 or 3 in relation to papillomavirus infection. N Engl J Med. 1992 Oct 29. 327(18):1272-8. [Medline].

  66. Kwikkel HJ, Helmerhorst TJ, Bezemer PD. Laser or cryotherapy for cervical intraepithelial neoplasia: a randomized study to compare efficacy and side effects. Gynecol Oncol. 1985 Sep. 22(1):23-31. [Medline].

  67. Kyrgiou M, Koliopoulos G, Martin-Hirsch P, Arbyn M, Prendiville W, Paraskevaidis E. Obstetric outcomes after conservative treatment for intraepithelial or early invasive cervical lesions: systematic review and meta-analysis. Lancet. 2006 Feb 11. 367(9509):489-98. [Medline].

  68. Martin-Hirsch PL, Paraskevaidis E, Kitchener H. Surgery for cervical intraepithelial neoplasia. Cochrane Database Syst Rev. 2000. (2):CD001318. [Medline].

  69. Montz FJ. Management of high-grade cervical intraepithelial neoplasia and low- grade squamous intraepithelial lesion and potential complications. Clin Obstet Gynecol. 2000 Jun. 43(2):394-409. [Medline].

  70. Munoz N, Bosch FX, de Sanjose S. The causal link between human papillomavirus and invasive cervical cancer: a population-based case-control study in Colombia and Spain. Int J Cancer. 1992 Nov 11. 52(5):743-9. [Medline].

  71. National Cancer Institute. The 1988 Bethesda System for reporting cervical/vaginal cytological diagnoses. National Cancer Institute Workshop. JAMA. 1989 Aug 18. 262(7):931-4. [Medline].

  72. Persad VL, Pierotic MA, Guijon FB. Management of cervical neoplasia: a 13-year experience with cryotherapy and laser. J Low Genit Tract Dis. 2001 Oct. 5(4):199-203. [Medline].

  73. Pinto AP, Crum CP. Natural history of cervical neoplasia: defining progression and its consequence. Clin Obstet Gynecol. 2000 Jun. 43(2):352-62. [Medline].

  74. Popkin DR, Scali V, Ahmed MN. Cryosurgery for the treatment of cervical intraepithelial neoplasia. Am J Obstet Gynecol. 1978 Mar 1. 130(5):551-4. [Medline].

  75. Solomon D, Davey D, Kurman R, et al. The 2001 Bethesda System: terminology for reporting results of cervical cytology. JAMA. 2002 Apr 24. 287(16):2114-9. [Medline].

  76. Soutter WP, Sasieni P, Panoskaltsis T. Long-term risk of invasive cervical cancer after treatment of squamous cervical intraepithelial neoplasia. Int J Cancer. 2006 Apr 15. 118(8):2048-55. [Medline].

  77. Townsend DE, Richart RM. Cryotherapy and carbon dioxide laser management of cervical intraepithelial neoplasia: a controlled comparison. Obstet Gynecol. 1983 Jan. 61(1):75-8. [Medline].

  78. Wright TC Jr. HPV DNA testing for cervical cancer screening. FIGO 6th Annual Report on the Results of Treatment in Gynecological Cancer. Int J Gynaecol Obstet. 2006 Nov. 95 Suppl 1:S239-46. [Medline].

  79. Wright TC Jr, Massad LS, Dunton CJ, Spitzer M, Wilkinson EJ, Solomon D. 2006 consensus guidelines for the management of women with abnormal cervical cancer screening tests. Am J Obstet Gynecol. 2007 Oct. 197(4):346-55. [Medline].

  80. Wright TC Jr, Massad LS, Dunton CJ, Spitzer M, Wilkinson EJ, Solomon D. 2006 consensus guidelines for the management of women with cervical intraepithelial neoplasia or adenocarcinoma in situ. Am J Obstet Gynecol. 2007 Oct. 197(4):340-5. [Medline].

  81. Wright VC, Davies EM. The conservative management of cervical intraepithelial neoplasia: the use of cryosurgery and the carbon dioxide laser. Br J Obstet Gynaecol. 1981 Jun. 88(6):663-8. [Medline].

 
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Cervical carcinoma with adnexa.
Squamous cell cervical carcinoma.
Punctation in cervical lesions. Left is fine, right is coarse (likely high grade or invasive).
Table. Rates of Progression of CIN [6]
CIN % Regression % Persistence % Progression
CIN 1 57 32 11
CIN 2 43 35 22
CIN 3 32 56 12
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