|Other common terms: HPV, papillomavirus, warts (symptom)|
|ICD-10 classification: B97.7|
|Prevalence: Very common; exact incidence of HPV is unknown.|
|Causes: Direct contact.|
|Treatments/cures: A vaccine for certain strains of HPV has been developed in recent years. General warts are treated with a range of topical medications or minor surgery.|
Human Papilloma Virus (HPV) typically infects the cells of the skin and results in warts. Warts are an abnormal skin growth on the skin, taking on a variety of different appearances, and in any region of skin. These may occur at any location on the skin, and even on mucous membranes, such as genitalia. In some cases, pain, pruritus (itching), or local irritation may occur. While most HPV infection is benign and is not immediately life-threatening, dysplastic change or tumours may form. The most common of these are cervical and anal cancers resulting from genital or anal HPV infection.
Human papilloma viruses (HPVs) belong to the Papillomavirus family and over 100 genotypes of HPV exist. HPV infections also have a causal relationship with cervical cancer.
Cutaneous warts are a relatively common problem yet surveillance data of cutaneous warts in the community is limited.
One report from a sample of 2491 students in Victoria, Australia, indicated an overall prevalence of cutaneous warts of 22%. The incidence of warts in the community (i.e. among adults) is not available. However, one study described occupations involved with meat, poultry, and fish processing to be associated with increased risk of getting warts.
Data on genital warts is also lacking. Indigenous Australian women in the Northern Territory were reported to have a HPV prevalence of 42%. In a study of 69,147 women from Denmark, Iceland, Norway, and Sweden, 10.6% were reported to have had genital warts.
Cervical cancer incidence
Not all HPV infections result in warts. As such, cervical cancer may develop in a woman without ever having had genital warts. Similarly, not all HPV infections result in dysplastic transformation. Some HPV types have a higher propensity to develop into cancers. HPV 16 was isolated in 53.8% of patients with cervical cancer in Australia; HPV 18 was isolated in 17.2%. An association was also found between HPV 18 and adenocarcinomas. A meta-analysis also support that the commonest HPV types associated with cervical cancer are HPV16 and HPV18. Regional variation exists; HPV 58 and HPV 52 were more frequently identified in Asia.
There were an estimated 493,000 new cases of cervical cancer and 274,000 mortalities worldwide in 2002. The incidence and mortality rates are higher in developing countries than developed countries; in Australia, the incidence is 7.40 per 100,000, and mortality rate is 2.0 per 100,000 persons. Screening programs have resulted in decline; cervical cancer was previously the most common cancer in women in developed nations. It is now the second most common cancer in women, and seventh most common in the world.
HPV transmission usually occurs via direct contact. Direct transmission to skin usually requires the integrity of skin to be compromised. Abrasions and excoriations are generally required. In addition, because of the resistance of the virus to the environment, a virus particle on an inanimate object may in theory result in an infection.
Even though transmission occurs mainly through direct contact, normal skin is quite resistant to inoculation. As such, a deficit in skin integrity is usually required. Individuals with known warts are generally advised not to scratch them; doing so may result in localized spread and worsening of the condition. It has also been suggested that warts can be spread by inanimate objects; this is due to HPV resistance to inactivation by environmental factors (e.g. heat/ cold). Objects in public places such as toilet seats may be able to spread the virus. Frequent visits to public swimming pools may also predispose to HPV infection.
Genital warts are spread via genital contact. As such, it is its incidence rises with increasing sexual activity. The use of condoms has been suggested to reduce spread; however, this form of prevention is not completely protective.
Risk factors for acquiring genital warts include:
- Younger age;
- Number of lifetime sexual partners;
- Lack of or inconsistent condom use.
Cancers (in particular cervical cancers) result when normal cellular growth regulations are disrupted beyond recovery. Excessive proliferation of cells results in cancerous change.
Infection and spread
Human papilloma viruses (HPVs) belong to the Papillomavirus family. Their genetic material consists of circular deoxyribonucleic acid (DNA). This genetic material is contained within a protein capsid. However, unlike some viruses, this virus does not have a lipid membrane. This lack of lipid membrane gives the virus more resistance to environmental factors.
The virus typically invades the basal cells of the skin. Viral particles are produced as the basal cells proliferate into keratinocytes and migrate to the superficial skin. These particles are contained within the skin cells and are released as the cells are cast off. Because the viral genes do not code for its own DNA polymerase, HPV relies heavily on host cell mechanisms to reproduce. This renders the virus resistant to drug treatments; fewer drug-specific proteins are available as drug targets to hinder virus production.
The proteins coded for by the HPV DNA are generally divided into two categories: E for early-phase proteins and L for late-phase proteins. Early phase proteins are involved in interfering with normal cell function, in order to promote abnormal cell growth and proliferation. In particular, E6 and E7 disrupt tumour suppressor genes (such as p53 and retinoblastoma) resulting in irregular growth patterns. The late stage proteins are expressed when infected cells have migrated closer to the skin surface. L1 and L2 form the protein capsid. These proteins are important in the pathogenicity of the virus. Because L1 and L2 are expressed only in the late stages, they are unable to stimulate the immune system to effectively remove the virus. By the time these proteins are expressed, the cells are relatively distant from the blood supply and are have thus effectively evaded the immune system. While antibodies against L1 and L2 are still produced, they are not manufactured in sufficient amounts. It is also on the basis of these proteins that the vaccine against HPV was developed. The vaccines consist of L1 and L2 proteins of specific HPV types. These assemble into virus-like-particles (VLPs) which when injected into humans, stimulating a more effective immune response. The body is then able to produce higher numbers of antibodies sufficient to combat the infection.
E6 and E7 proteins are important in the pathogenesis of cervical cancer. The genes encoding these proteins are retained or incorporated into cellular DNA. The inactivation of tumour suppressor genes over long periods of time results in dysplastic change and eventual cancer development. By this stage, L1 and L2 proteins are no longer expressed. Antibodies against L1 and L2 are no longer effective. Thus, the vaccines are only valid for preventative measures, and are not used for treatment.
Most patients may not even notice their own warts until they have reached a relatively large size. Warts are generally slow growing, and as such are not readily obvious. In addition, no other symptoms such as pain or itch alert the patient of its presence. These symptoms may rarely occur.
Patient complaints are generally for cosmetic reasons. Warts come in all shapes and sizes. They may be papular or nodular, with either a flat or rounded surface. Some may be spindle shaped, or even take the appearance of cutaneous horns. The presence of scale or hyperkeratosis is also variable. Pedunculated warts also exist. The size of warts may vary considerably.
Several commonly seen warts have been described such as:
- Common warts
- Flat warts
- Filiform warts
- Mosaic warts
- Plantar warts
- Genital warts
In-depth descriptions are available on the Better Health Channel (see references).
Cervical cancer diagnosis and symptoms
Under current screening regimens, cervical cancers are generally detected prior to their symptomatic stage. It is recommended that all women who are (or have been) sexually active receive regular pap smears (once every one to two years). Symptoms that may occur may include abnormal bleeding (i.e. between menstrual cycles; during or after sexual intercourse), or pelvic pain.
Treatment options for warts vary with location:
- Topical keratolytics (i.e. salicylic acid, Upton’s paste)
- Ablative therapy (ie. Cautery)
- Immune modulators (i.e. imiquimod)
- Immunotherapy (topical sensitizers, dinitrochlorobenzene, diphencyprone)
- Keratolytics (i.e. salicylic acid, Upton’s paste)
- Periodic cryotherapy
- Immune modulators (i.e. imiquimod)
- Hydocortisone (to reduce irritation/ symptomatic relief)
- Keratolytics (i.e. salicylic acid, Upton’s paste)
Topical salicylic acid
Topical salicylic acid has been regarded as one of the more effective therapies against warts. Pooled data from multiple trials suggests a cure rate of 75%. Side effects such as cellulitis and minor skin irritation have been reported. Other major side effects are generally not seen.
Cryotherapy involves the use of liquid nitrogen to freeze warts, effectively killing the cells. Trials have suggested its effectiveness to be similar to the use of topic salicylic acid. However, severe side effects may result. The most common complaints are pain and blistering (up to 64%), particularly with more aggressive therapy. Several participants have withdrawn from studies due to these side effects.
The use of topical imiquimod for genital or perianal warts has been supported by multiple studies. The most common side effect was skin irritation. Imiquimod is believed to stimulate the immune system, in particular by increasing the production of interferon. This typically results in localized inflammation, and may be related to irritation reported by some users.
Retinoids are analogues of Vitamin A and functions by inhibiting growth and differentiation of the epidermis. The effectiveness of retinoids in children has been reported in two separate trials. In one group of 25 participants, 42.3% experienced skin erythema and peeling. Similar data involving adults is not available.
Podophyllotoxin and Podophyllum are used to treat warts due to their anti-mitotic activity (Therapeutic Guidelines, 2004b). While treatment of warts with these agents have had some success, other forms of treatments are generally more effective.
Resistant warts may be treated with diphencyprone. 60% of patients in a study responded positively to treatment. Topical dinitrochlorobenzene may also be used; a cure rate of 80% has been reported.
Several trials on the effectiveness of intra-lesional bleomycin have produced inconsistent findings. Cure rates in these studies ranged between 16 and 94%. Localized skin reactions such as an erythematous rash, hyperpigmentation, and tenderness may result. However, more serious side effects such as anaphylactoid reactions and even pulmonary fibrosis have been reported.
The use of duct tape has also bee proposed. One study found the use of duct tape to be more efficacious than cryotherapy. Duct tape was applied on the warts for six days, and was replaced if displaced. Following the end of this period, the duct tape was removed. The site of the wart was soaked in water, and then debrided with either an emery board or pumice stone. The duct tape was replaced the next day. This treatment continued for a maximum of two months or until the wart had resolved. Complete resolution was seen in 85% of participants treated with duct tape as compared to 60% in patients treated with cryotherapy. Cervical cancer treatments Treatment for cervical cancer also varies, but depending on the staging of the cancer. In general, surgical management is used with adjunct chemotherapy and/or radiotherapy where necessary. Staging of the tumour depends on the extent of its growth. Early detection via screening greatly improves survivability. Commons treatments for cervical cancer include:
- Conization – removal of a section of the cervix and cervical canal; this sample may be used as part of staging and/or grading the cancer
- Hysterectomy – removal of the cervix and the uterus
- Radical hysterectomy – removal of the uterus, cervix, and part of the vagina; the ovaries, fallopian, and local lymph nodes may also be removed
- Pelvic exenteration – removal of cervix, vagina, ovaries, and local lymph nodes, as well as lower colon, rectum, and bladder
- Cryosurgery (see above)
- Laser surgery
- X-rays are used to irradiate the cancer cells to kill them or minimize growth
- Drugs are used to kill the cancer cells. The mechanism of action of different drugs varies. However, because of the similarities between cancer cells and normal cells, severe side effects may result
Cutaneous HPV may be avoided by minimizing contact with individuals who have warts. Yet, because of the resistance of the virus to environmental agents, there is a theoretical risk that HPV infection can be acquired from inanimate objects. Genital HPV infection could be minimized by consistent condom use in sexual activity. Despite this, HPV infection is still likely to occur.
A HPV vaccine has been released in recent years. The vaccine is a quadrivalent vaccine and protects against HPV 16 and 18 (two most common causes of cervical cancer), & HPV 6 and 11. Because there is a range of various other HPV types that may cause genital warts and cervical cancer, no one is fully protected. The vaccine only protects against the HPV types that are the most common causes of cervical cancer and genital warts. Because prevention is not 100% effective, active surveillance is still required. It is recommended that women who have had the vaccine continue to receive regular pap smears to ensure that any malignant change is detected early with appropriate follow-up treatment(s) initiated.
Australia’s HPV vaccination program
In Australia, the National HPV Vaccination Program began in April 2007. Under this program, young girls aged 12-13 whose parents consent will be provided the HPV vaccine for free. Girl and young women between the age of 14 and 26 were eligible for free vaccine. The vaccine can be provided at school for school-goers, and at general practice surgeries or community immunization clinics for non-school-goers. The free vaccination was only available for females aged 14-26 until the end of June 2009.
The vaccination course occured over a six month period:
- First dose at an elected date
- Second dose two months following first dose
- Third dose six months following first dose
The HPV vaccine does not have Therapeutic Goods Administration (TGA) approval for women over the age of 26.
TGA approval has been obtained for males aged between 9 to 15 years. However, evidence supporting the effectiveness of providing the vaccine for men is limited. As such, the free vaccine is not available for men.
Other nations have also incorporated the HPV vaccine into their vaccination programs. The vaccine is available for free in the United Kingdom, and in select provinces/territories in Canada. The vaccine is available but not publicly funded in some countries such as New Zealand.
The prognosis of cutaneous warts is generally good. A variety of therapies are available with relatively good success rates. Some warts may eventually disappear even without treatment. Those that are refractory to treatment are generally benign.
The mortality rate from cervical cancer is relatively low. The prognosis of the cervical cancer is variable depending on the staging of the cancer. This includes factors such as:
- The size of the tumour
- The extent of invasion into the cervix
- Invasion to local or neighbouring structures
- Metastases to local lymph nodes
- Metastases to other solid organs
- Specific histopathological findings
- Androphy, E J (2007). ‘Human papillomaviruses and warts’. Schaecter’s Mechanisms of Microbial Disease. 399-405. Lippincott Williams & Wilkins.
- Androphy, E J & Lowy, D R (2008). ‘Chapter 196: Warts’. Fitzpatrick’s Dermatology in General Medicine (7th Edition). The McGraw-Hill Companies.
- Beutner, K. R., Tyring, S. K., Trofatter, K. F. Jr., Douglas, J. M. Jr., Spruance, S., Owens, M. L. et al. (1998). Imiquimod, a patient-applied immune-response modifier for treatment of external genital warts. Antimicrobial Agents and Chemotherapy, 42(4), 789-794. Available online. [Accessed on 11/12/2008].
- Bosch, F X, Lorincz, A, MuÃ±oz, N, Meijer, C & Shah, K V (2002). ‘The causal relation between human papillomavirus and cervical cancer’. Journal of Clinical Pathology, 55, 244-265. Abstract available online. [Accessed on 11/12/2008].
- Bowden, F J, Paterson, B A, Savage, J, Fairley, C K, Garland, S M & Tabrizi, S N (1999). ‘Estimating the prevalence of Trichomonas vaginalis, Chlamydia trachomatis, Neisseria gonorrhoeae, and human papillomavirus infection in indigenous women in Northern Australia’. Sexually Transmitted Infections, 75(6), 431-434. Abstract available online. [Accessed on 11/12/2008].
- Chen, S, O’Sullivan, H, Tabrizi, S N & Fairley, C K (1999). ‘Prevalence and genotyping of HPV in cervical cancer among Australian women’. International Journal of Gynecology & Obstetrics, 67(3), 163-168. Abstract available online. [Accessed on 11/12/2008].
- Clifford, G M, Smith, J S, Plummer, M, MuÃ±oz, N & Franceschi, S (2002). ‘Human papillomavirus types in invasive cervical cancer worldwide: A meta-analysis’. British Journal of Cancer, 88, 63-73. Available online. [Accessed on 11/12/2008].
- Department of Health and Ageing. (2008). Preventing Cervical Cancer. The National HPV Vaccination Program [Online]. [Accessed on 11/12/2008, no longer online].
- Focht, D R, Spicer, C & Fairchok, M P (2002). ‘The efficacy of duct tape vs cryotherapy in the treatment of verruca vulgaris (the common wart)’. Archives of Pediatrics & Adolescent Medicine, 156(10), 971-974. Available online. [Accessed on 12/12/2008].
- Gibbs, S Harvey, I, Sterling, J & Stark, R (2002). ‘Local treatments for cutaneous warts: Systematic review’. British Medical Journal, 325, 461. [Accessed on 11/12/2008, no longer online].
- Gelmetti, C, Cerri, D, Schiuma, A A & Menni, S (1987). ‘Treatment of extensive warts with etretinate: A clinical trial in 20 children’. Paediatric Dermatology, 4(3), 254-258. Abstract available online. [Accessed on 11/12/2008].
- Kilkenny, M & Marks, R. (1998). ‘The descriptive epidemiology of warts in the community’. Australasian Journal of Dermatology, 37(2), 80-86. [Accessed on 11/12/2008]
- Kilkenny, M, Merlin, K, Young, R & Marks, R (1998). ‘The prevalence of common conditions in Australian school students: 1. Common, plane, and plantar viral warts’. British Journal of Dermatology, 138, 840-845. Available online. [Accessed on 11/12/2008].
- KjÃ¦r, S K, Tran, T N, Sparen, P, Tryggvadottir, L, Munk, C & Dasbach, E et al. (2007). ‘The burden of genital warts: A study of nearly 70,000 women from the general female population in the 4 Nordic countries’. The Journal of Infectious Diseases, 196, 1447-1454. Available online. [Accessed on 11/12/2008].
- Kubeyinje, E P (1996). ‘Evaluation fo the efficacy and safety of 0.05% tretinoin cream in the treatment of plane warts in Arab children’. Journal of Dermatological Treatment, 7(1), 21-22. [Accessed on 11/12/2008].
- National Cancer Institute. (2008). Treatment Option Overview. Cervical Cancer Treatment [Online]. Available online. [Accessed on 11/12/2008]
- National Health Service, United Kingdom. (2008). Vaccines: HPV. [Online] Available online. [Accessed on 12/12/2008].
- Parking, D M, Bray, M, Ferlay, J & Pisami, P (2005). ‘Global cancer statistics, 2002’. A Cancer Journal for Clinicians, 55, 74-108. Available online. [Accessed on 11/12/2008].
- Public Health Agency of Canada. (2007). Human papillomavirus (HPV) prevention and HPV vaccine: Questions and answers. [Online] Available online. [Accessed on 12/12/2008].
- Rampen, F H J & Streijlen, P M (1996). ‘Diphencyprone in the management of refractory palmoplantar and periungual warts: An open study’. Dermatology, 193(3), 236-238. Abstract available online. [Accessed on 11/12/2008].
- RxList Inc. (2008). Blenoxane: Side effects & drug interactions. RxList, The Internet Drug Index [Online]. Available online. [Accessed on 11/12/2008].
- Sauder, D N, Skinner, R B, Fox, T L & Owens, M L (2003). ‘Topical imiquimod 5% cream as an effective treatment for external genital and perianal warts in different patient populations’. Sexually Transmitted Diseases, 30(2), 124-128. Available online. [Accessed on 11/12/2008].
- State of Victoria. (2007). Better Health Channel: Warts [Online]. Available online. [Accessed on 10/12/2008].
- Sterling, J C, Hand-field Jones, S & Hudson, P M (2001). ‘Guidelines for the management of cutaneous warts’. British Journal of Dermatology, 144, 4-11. Available online. [Accessed on: 11/12/2008].
- Stone, K M, Becker, T M, Hadgu, A & Krus, S J (1990). ‘Treatment of external genital warts: A randomized clinical trial comparing podophyllin, cryotherapy, and electrodessication’. Genitourinary Medicine, 66, 16-19. Abstract available online. [Accessed on 11/12/2008]
- The New Zealand HPV Project. (2007). HPV Vaccine. [Online] Available online. [Accessed on 12/12/2008].
- Therapeutic Guidelines Ltd. (2004a). ‘Infectious diseases’. Therapeutic Guidelines: Dermatology 2nd Edition. 201-220. Therapeutic Guidelines Limited.
- Therapeutic Guidelines Ltd. (2004b). ‘Getting to know your drugs’. Therapeutic Guidelines: Dermatology 2nd Edition. 25-53. Therapeutic Guidelines Limited.
- Tyring, S K, Aranyi, I, Stanley, M A, Tomai, M A, Miller, R L, Smith, M H et al. (1998). ‘A randomized, controlled, molecular study of condylomata acuminata clearance during treatment with imiquimod’. The Journal of Infectious Diseases, 178, 551-555. Abstract available online. [Accessed on 11/12/2008].
- Wen, L W, Estcourt, C S, Simpson, J M & Midel, A (1999). ‘Risk factors for the acquisition of genital warts: Are condoms protective?’ Sexually Transmitted Infections, 75(5), 312-316. Abstract available online. [Accessed on 11/12/2008].