ࡱ>  \bjbj 0p"gp"gVV#########&<#U$(2V*V*V*V*1+4e+ q+$#y+1+1+y+y+##V*V*CCCy+X#V*#V*Cy+CC:N V*:Az=d%0U e=e  e# y+y+Cy+y+y+y+y+@y+y+y+Uy+y+y+y+ey+y+y+y+y+y+y+y+y+VX ": 2020 European guideline for the management of balanoposthitis Sarah K. Edwards1, Christopher B. Bunker2, Eric M. van der Snoek3 and Willem I. van der Meijden4 Affiliations: iCasH Suffolk, Abbey View Clinic, Bury St Edmunds, UK Department of Dermatology, University College London Hospitals, London, UK Department of Dermatology, Central Military Hospital, Utrecht, The Netherlands Department of Dermatology, Barnsley Hospital NHS Foundation Trust, Barnsley, South-Yorkshire, UK Introduction The main objective of this guideline is to aid recognition of the symptoms and signs and complications of penile skin conditions that may present to a variety of clinical specialists in Europe, including dermatology, sexual health or urology1. This guideline concentrates on a selected group of conditions, which may be managed by clinicians practising in these disciplines, either alone or in conjunction with other specialists. It is not intended as a comprehensive review of the treatment of all forms of balanoposthitis. It is aimed primarily at people aged 16 years or older. This guideline offers recommendations on the diagnostic tests and treatment regimes needed for the effective management of balanoposthitis and includes the following penile conditions: Candidal balanoposthitis Anaerobic balanoposthitis Aerobic balanoposthitis Lichen sclerosus Lichen planus Zoons (plasma cell) balanoposthitis Psoriasis and circinate balanoposthitis Eczema (including irritant, allergic and seborrheic) Non-specific balanoposthitis Fixed drug eruptions Premalignant conditions: Penile intra epithelial neoplasia (PeIN) Bowenoid papulosis Bowens disease Erythroplasia of Queyrat Aetiologies Balanitis describes inflammation of the glans penis, posthitis inflammation of the prepuce. In practice both areas are often affected and the term balanoposthitis is then used. It is a collection of disparate conditions with similar clinical presentation and varying aetiologies affecting a particular anatomical site (see table 1). Balanitis is uncommon in circumcised men2 and in many cases preputial dysfunction is a causal or contributing factor. Table 1. Conditions affecting the glans and prepuce3,4,5 InfectiousInflammatory DermatosesPremalignant Penile intraepithelial neoplasia (PeIN) Candida albicansLichen sclerosus Bowens disease Streptococci Lichen planus Bowenoid papulosisAnaerobesPsoriasis and circinate balanitisErythroplasia of QueyratStaphylococciZoon's balanitis  Trichomonas vaginalisEczema (including irritant, allergic and seborrheic)Herpes simplex virusAllergic reactions (including fixed drug eruption and Stevens Johnson Syndrome)Human papillomavirusMycoplasma genitaliumSyphilis Other, rarer dermatoses are not included in this table. Infections, especially with candida, may often be secondary to primary inflammatory dermatoses. General Management of the Patient with Balanoposthitis4,5,6 Clinical Features Symptoms and signs vary according to aetiology and specific conditions are covered in more detail individually. Descriptions of the typical appearances of certain balanitides are given separately in the management section. Diagnosis Balanitis and balanoposthitis are descriptive terms covering a variety of unrelated conditions, the appearances of which may be suggestive but should never be thought to be pathognomonic. Biopsy7 is sometimes needed to exclude pre-malignant disease. The following investigations are intended to aid diagnosis in cases of uncertainty: Sexual history taken, with specific questioning on sexual risk taking Sub-preputial swab for Candida spp and bacterial culture - should be undertaken in most cases to exclude an infective cause or superinfection of a skin lesion or dermatosis Urinalysis for glucose - appropriate in some cases but especially if candidal infection is suspected. HSV nucleic acid amplification test (NAAT) - if ulceration present. Treponema pallidum (TP) NAAT and/or dark ground examination for spirochaetes (where available) - if an ulcer is present, or alternatively syphilis serology with follow up at 3 months. NAAT for Trichomonas vaginalis - particularly if a female partner has an undiagnosed vaginal discharge Full routine screening for other sexually transmitted infections (STIs) - particularly screening for Chlamydia trachomatis infection / non-specific urethritis if a circinate-type balanitis is present Dermatology opinion for dermatoses and suspected allergy Biopsy - if the diagnosis is uncertain and the condition persists6,7 Management The aims of management are to minimise sexual dysfunction, to minimise urinary dysfunction, to exclude penile cancer, to treat pre-malignant disease and to diagnose and treat sexually transmitted diseases. Predisposing factors for balanoposthitis include poor hygiene and overwashing, and non-retraction of the foreskin, and some medical conditions such as diabetes mellitus.. Many cases of balanoposthitis seen in practice are a simple intertrigo i.e. inflammation between two layers of skin with bacterial or fungal overgrowth. Good personal hygiene, washing daily, avoiding irritants (such as soap), and keeping the foreskin retracted until the glans penis is dry (advising the patient of the risk of paraphimosis especially if the prepuce is tight) can be effective, but compliance may be challenging. General Advice Avoid soaps while inflammation is present5,8 Advise about risks of condom failure if creams are being applied Patients should be given a detailed explanation of their condition with particular emphasis on any implications for their health (and that of their partner where a sexually transmissible agent is found). Management of specific balanitides Infective balanoposthitis A range of infective agents have been isolated more frequently in men with balanoposthitis, and may not be easily differentiated by clinical findings.9 These include viral infections such as Human papillomavirus (HPV) and Herpes simplex virus (HSV), fungal infections including a variety of Candida spp, and bacterial infections such as Staphylococcus spp10, Streptococcus spp11,12. Asymptomatic carriage of organsims may also be associated with subclinical inflammation and a greater risk of Human Immunodficiency virus (HIV) infection13. Sexually transmitted infections such as Trichomonas vaginalis, syphilis14 and more recently Mycoplasma genitalium15 .have been reported as causing balanoposthitis. Candidal balanoposthitis (less than 20% of cases) Clinical Features Symptoms: erythematous rash with soreness and/or itch Appearance: blotchy erythema with small papules which may be eroded, or dry dull red areas with a glazed appearance. Older age has been identified as a risk factor16 Diagnosis Sub-preputial culture (n.b. isolation of candida on culture does not prove causality, as it may represent opportunistic infection of other underlying dermatoses) Consider urinalysis for glucose Investigation for other causes e.g. HIV or other causes of immunosuppression if balanitis is severe or persistent Many dermatologists believe that this primary diagnosis is very rare even in HIV infection (apart from in diabetes mellitus (DM)) and that candida is almost always an opportunistic pathogen, signifying an underlying dermatosis. Management Recommended regimens17 Clotrimazole cream 1%18(Ib,A) Miconazole cream 2%19(IIa,B) Apply twice for 7-14 days. Alternative regimens Fluconazole 150mg stat orally18(Ib, A)- if symptoms severe Nystatin cream19 100 000units/gm - if resistance suspected, or allergy to imidazoles (IIa,B) Topical imidazole with 1% hydrocortisone - if marked inflammation is present17(IV, C) Although there has been an increase in reports of drug resistance in serious candidal infection, there is no new evidence pertaining to treatment of candidal balanitis Sexual partners As there is a high rate of candidal infection in sexual partners, they should be offered testing for candida or empiric anti-candidal treatment to reduce the reservoir of infection in the couple. Follow up Not required unless symptoms and signs are particularly severe or an underlying problem is suspected. Anaerobic infection13, 20 Clinical Features Symptoms: foul smelling sub preputial inflammation and discharge, in severe cases associated with swelling and inflamed inguinal lymph nodes Appearance: preputial oedema, superficial erosions; milder forms also occur. Diagnosis Gram stain may show Fusiform / mixed bacterial picture Sub-preputial NAAT (to exclude other causes e.g. Trichomonas vaginalis) Gardnerella vaginalis is a facultative anaerobe which may be isolated Swab for herpes simplex virus infection if ulcerated Management Advice about genital hygiene. Circumicision may be required in recurrent cases or if phimosis is present Recommended regimen Metronidazole 400 - 500mg twice daily x 1 week (IV, C) The optimum dosage schedule for treatment is unknown. Milder cases may respond to topical metronidazole Alternative regimen Co-amoxiclav 375mg three times daily x 1 week Clindamycin cream applied twice daily until resolved These treatments have not been assessed in clinical trials (IV, C). Aerobic infection. Clinical Features Variable inflammatory changes including uniform erythema +/- oedema Diagnosis Sub-preputial culture Streptococcus spp and Staphylococcus aureus have been reported as causing balanitis10,11,12. Other organisms may also be involved. Management Treatment can be topical for mild symptoms Severe cases may require systemic antibiotics. Recommended regimens (IV,C) Depends on the sensitivities of the organism isolated. Mupirocin ointment 2-3 times per day for 7-10 days Trimovate cream once or twice daily for 7-10 days Severe cases may require systemic antibiotics while awaiting culture results21 Oral flucloxacillin500 mg four times a day for sevendays. Oral clarithromycin 250 mg twice daily for sevendays Alternative regimens Depends on the sensitivities of the organism isolated. Sexually Transmitted Infections (STIs) Balanoposthitis has been described with Herpes simplex virus Trichomonas vaginalis Mycoplasma genitalium15 Syphilis14 Management is as per specific guidelines Lichen sclerosus 4,6,22,23,24,25,26 Aetiology An inflammatory scarring skin condition; although an autoimmune pathogenesis has been postulated, it may be due to chronic occluded contact with urine in the uncircumcised27. The condition occurs in all ages. It is probably responsible for many cases of phimosis in childhood6. Obesity, congenital and acquired anatomical abnormalities (hypospadias), piercing and urological surgery are predisposing factors. Clinical Features6, 22, 23, 24, 26, 27 Symptoms Itching, soreness, splitting, haemorrhagic blisters, dyspareunia, problems with urination including post micturition micro-incontinence or dribbling. May be asymptomatic. Signs Typical appearance: lichenoid (lilac) balanoposthitis with white patches on the glans, often with involvement of the prepuce. There may be subtle or florid Zoonoid inflammation and also haemorrhagic vesicles, purpura and rarely blisters and ulceration. Architectural changes include blunting of the coronal sulcus, destruction of the frenulum, phimosis or waisting of the prepuce (constrictive posthitis), and meatal thickening and narrowing. Complications Phimosis and paraphimosis Urethral stenosis Penile intraepithelial neoplasia (PeIN) and malignant transformation to squamous cell carcinoma. The published risk ranges from 0-12.5%6, 24, 25, 28. In established penis cancer the association with lichen sclerosus is thought to be about 50% (the other 50% being associated with HPV) 29 Extra-genital disease can occur. In contrast with females perianal disease is uncommon. Diagnosis Typical clinical features Biopsy: this initially shows a thickened epidermis which then becomes atrophic with follicular hyperkeratosis. This overlies a band of dermal hyalinisation with loss of the elastin fibres, with an underlying perivascular lymphocytic infiltrate. Biopsy should only be carried out by experienced practitioners. A negative biopsy does not exclude lichen sclerosus, and a positive biopsy does not exclude squamous cell carcinoma or PeIN elsewhere. The choice of the area biopsied is important both in terms of the risks and in getting an adequately representative sample. Histological interpretation can be difficult and needs clinico-pathological correlation. Management, 22, 23, 24, 25, 26, 30 Recommended regimens Soap free washing, avoidance of contact with urine, barrier preparations, weight loss, removal of genital jewellery 24, 25, 26, 30, 31, Ultrapotent topical steroids22, 23, 24, 25, 26, 32, 33 (e.g. clobetasol proprionate) applied twice daily for a month then ceased and replaced with a barrier preparation. Intermittent use to maintain remission is not encouraged. 50-60% of patients are treated successfully in this way.22,25,26 A double-blind study in children showed response to topical mometasone furoate particularly in early cases without scarring34. ( Ia,A) Patients with a history of genital warts should be warned about the risk of a relapse (adjunctive HPV vaccination can be considered35). Prophylactic aciclovir or equivalent should be prescribed in patients with a history of active genital herpes simplex infection (IV, C). Secondary bacterial or candidal infection should be treated Alternative regimens Although topical calcineurin inhibitors have been claimed to be efficacious32, 36 (pimecrolimus applied twice daily, Ib,A) stinging after initial application may occur and can be minimised by use of emollients. There is concern about the development of malignancy37 in case of continuous long-term use, although there have been no systematic reviews of the risk in lichen sclerosus31. Circumcision is indicated for a) failed topical medical treatment or b) persistent requirement for daily topical treatment.22,24,25 Surgery may be indicated to address symptoms due to persistent phimosis or meatal stenosis and urethral disease (III,B) This may include circumcision, meatotomy, glans resurfacing, urethroplasty and bariatric surgery. 4, 22, 23, 24, 25, 26, 30,38,39 Follow up (IV, C) 22,24,25,30 Patients deemed to be cured by medical or surgical treatment can be discharged with the caveat that although low (especially after circumcision) there are risks of recurrence, urethral disease and neoplastic change, so they should keep an attentive watch on their genitalia and report any changes promptly to their GP. GPs should have a low threshold for re-referral (especially if they put on weight and develop a neo-foreskin). Lichen planus6 Aetiology Lichen planus is an inflammatory disorder with manifestations on the skin, genital and oral mucous membranes. More rarely it affects the conjunctiva and oesophagus. It is an inflammatory condition of unknown pathogenesis, but it is thought to have an immunological basis. The association with hepatitis C is controversial40. Certain drugs, most frequently ACE-inhibitors, beta blockers, NSAIDs and thiazide diuretics, and biologics may cause lichen planus like eruptions41, 42. Clinical Features Symptoms: Change in appearance, more rarely itch and soreness / dyspareunia. It may also be asymptomatic. Clinical appearance: Purplish well demarcated plaques (can be on glans and prepuce and on the shaft of the penis), alternatively erosive or annular lesions on the mucosal surfaces. Natural history: Mucosal lichen planus is often a chronic condition with remissions and exacerbations, in contrast to cutaneous lichen planus which tends to resolve spontaneously after 12-18 months. Diagnosis Clinical features of purplish lesions, or supporting evidence of lichen planus lesions elsewhere on the body (e.g. Whickhams striae). This particularly includes the mouth in cases of erosive (penogingival) disease. Biopsy: irregular saw-toothed acanthosis, increased granular layer and basal cell liquefaction. Band-like dermal infiltrate (mainly lymphocytic). The condition may very rarely be associated with pre-cancerous change6, 43 Management6, 44, 45 General advice Avoidance of irritants like soaps and shower gels The use of lubricants may be helpful in case of dyspareunia Recommended regimen Moderate to ultrapotent topical steroids (e.g. clobetasol proprionate ointment), depending on severity (for both mucosal and cutaneous disease) 44, 45. (III,B) Alternative regimens Topical and oral ciclosporin have been used for erosive disease 45,46,47, 48(IV,C) Topical calcineurin inhibitors can be efficacious36,45,48 (pimecrolimus applied twice daily, Ib, A). Stinging after initial application may occur and can be minimised by use of emollients. There is still concern about the risk of malignancy in case of continuous long-term use37, 49,50, 51 In severe cases oral prednisolone or acitretin may be necessary52. Circumcision: May be the treatment of choice for some cases of erosive lichen planus53 (IV,C) Follow up Atypical or persistent disease should receive more specialist input including biopsy Patients should be advised to contact the general practitioner or clinic if the appearances change. (IV, C) Zoons (plasma cell) balanitis6 Aetiology Zoons balanitis is a disease of uncircumcised males aged 40 years or older. It is thought to be due to irritation, partially caused by urine, in the context of a dysfunctional prepuce. It is generally regarded as a benign condition. Zoonoid inflammation (clinically and histologically) very frequently complicates other dermatoses, including precancer and cancer, but especially lichen sclerosus; this may be so common that it has been suggested that true Zoons balanitis may actually be rare or not even exist at all54. Clinical Features Symptoms: Change in appearance. Rarely bloodstained discharge. Rarely dyspareunia Clinical appearance: Includes well-circumscribed orange-red glazed areas on the glans and the inside of the foreskin, with multiple pinpoint redder spots - cayenne pepper spots. These are in a symmetrical distribution. Diagnosis Clinical features of symmetrical, well demarcated, shiny erythema of the glans and foreskin, however clinical distinction from other inflammatory and pre-malignant conditions is difficult and a high index of suspicion is recommended. Biopsy: early cases show epidermal thickening but this is followed by epidermal atrophy, at times with erosions. There is epidermal oedema (often mild) and a predominantly plasma cell infiltrate in the dermis with haemosiderin deposition and extravasated red blood cells55. Caveat: Zoonoid inflammation complicates other dermatoses and positive biopsy findings do not confirm the diagnosis or exclude neoplasia. Management6 . Recommended regimens Hygiene measures Management of underlying dermatoses54 Circumcision - this has been reported to lead to the resolution of lesions56 (IV, C) Topical steroid preparations - with or without added antibacterial agents e.g. Trimovate cream, applied once or twice daily.57 (IV,C) Antibacterial creams like mupirocin 2% ointment applied twice daily 58, 59, 60 (IV, C) Topical calcineurin inhibitors61,62 (IV,C) can be efficacious (pimecrolimus applied twice daily, Ib, A). There is still concern about the risk of malignancy51 in case of continuous long-term use. Stinging after initial application may occur and can be minimised by use of emollients Topical imiquimod 5% cream has been reported as helpful63 (IV,C) Alternative treatments Laser ablation - this has been used to treat individual lesions64, 65. (IV,C) Follow up Dependent on clinical course and treatment used, especially if topical steroids are being used long term. Penile biopsy should be performed if features are atypical or do not resolve with treatment. There are cases where even biopsies failed to identify pre-malignant disease. In case of doubt, repeated biopsies might therefore be useful.55 Psoriasis6,66,67 Clinical Features Symptoms: Change in appearance, soreness or itching. Appearance: In the circumcised male psoriasis on the glans is similar to the appearance of the condition elsewhere, with red scaly plaques. In the uncircumcised scaling is lost and the patches appear red and glazed. Diagnosis Is supported by evidence of psoriasis elsewhere. Biopsy may be necessary, particularly in case of a glazed appearance which can look similar to pre-malignant conditions such as Bowens disease and extramammary Pagets disease and other inflammatory conditions. The typical histological appearances include parakeratosis and acanthosis with elongation of rete ridges. There are collections of neutrophils in the epidermis. Maceration and secondary infection can modify appearances. Management 66, 67, 68 Although the number of studies assessing treatment efficacy have increased in the last decade, there is still a paucity of high-quality evidence concerning the efficacy and safety of topical and systemic treatments for inverse psoriasis68. Recommended regimen Moderate potency topical steroids67, 68 (+/- antibiotic and antifungal) (IV,C) Emollients Alternative regimens Topical Vitamin D preparations (calcipotriol or calcitriol applied twice daily)69 (IV,C) Topical bethamethasone dipropionate/calcipotriol ointment may be well tolerated in treatment of anogenital psoriasis, but potent steroids may not be indicated41 (IV,C) Topical calcineurin inhibitors have been used in small studies67, 68, 70 but should not be used as first line therapy (IV,C), and with caution in the uncircumcised.. . Circinate balanitis6 Aetiology This characteristic presentation may occur in isolation or be seen in Reiters disease a post infective syndrome, triggered by urethritis or enteritis in genetically predisposed individuals. It consists of skin problems, joint problems and ocular problems, with other systems affected more rarely. There is overlap with psoriasis in some cases. It has been reported in association with HIV infection. Clinical Features Signs Typical appearance: greyish white areas on the glans which coalesce to form geographical areas with a white margin. It may be associated with other features of Reiters syndrome but can occur without. Diagnosis On clinical appearance in association with other features of Reiters syndrome Biopsy: spongiform pustules in the upper epidermis, similar to pustular psoriasis. Management (IV, C) Further Investigation Screening for STIs. Syphilis can also give rise to similar features71. Consider testing for HLAB27. A positive test can confirm a diagnosis and provide important information about the risk of associated disease, such as urethritis, gastrointestinal disease and arthritis. Recommended regimen See under Psoriasis Treatment of any underlying infection Sexual partners If an STI is diagnosed, the partner(s) should be treated as per the appropriate protocol. Follow up May be needed for persistent symptomatic lesions. Associated STIs should be followed up as per appropriate guidelines. Eczema6 Irritant / allergic balanitis-balanoposthitis72, 73 Aetiology Symptoms can be associated with irritants, such as more frequent genital washing with soap, a history of atopy, or exposure to topical agents suggesting delayed hypersensitivity. In a small number of cases a history of a precipitant may be obtained and common allergens are often found in intimate hygiene products e.g. preservatives and fragrances74 It may arise as a primary condition, but is regularly encountered as a secondary phenomenon in the presence of a pre-existing genital dermatosis. Clinical Features Appearance: ranges from mild non- specific erythema to widespread oedema of the penis. Diagnosis Patch tests: referral to a dermatologist is useful if allergy is suspected. Biopsy: eczematous with spongiosis and non-specific inflammation. Culture: to exclude superinfection Management74 General Advice Avoidance of precipitants - especially soaps.8 Use of low-allergy products Emollients - applied as required and used as a soap substitute.8 Recommended Regimen Hydrocortisone 1% applied once or twice daily until resolution of symptoms. (IV, C) Alternative Regimen In more florid cases more potent topical steroids may be required and may need to be combined with antifungals and/or antibiotics Calcineurin inhibitors (tacrolimus/pimecrolimus)76 Follow up Not required, although recurrent problems are common and the patient needs to be informed of this. Seborrheic dermatitis Aetiology Hypersensitivity to Malassezia furfur (Pityrosporum ovale) Clinical features Mild itch or redness - scaling is less likely at this site. Diagnosis Supported by classical findings at other sites (nasolabial folds, scalp, ears, eyebrows) Management There is a paucity of evidence specifically for balanitis, and low quality evidence for other sites77, 78 Recommended regimen Antifungal cream with a mild to moderate steroid.(IV,C) Alternative regimens6 Oral azole e.g. itraconazole (IV,C) Oral tetracycline (IV,C) Oral terbinafine may be effective79(Ib, A) Non- specific balanoposthitis (IV,C)6 Aetiology: Unknown Clinical features: Chronic symptomatic presentation with relapses and remissions or persistence. No unifying diagnosis and poor response to a range of topical and oral treatments. Diagnosis: Failure to respond to maximal topical steroid and antifungal treatments (including potent steroids). Non specific histology on biopsy. Non specific histology at circumcision. No evidence of underlying infective cause (e.g. Chlamydia or mycoplasma) Management: Circumcision is curative Fixed drug eruption (IV,C)80 Aetiology An uncommon condition, but the penis is one of the more commonly affected areas of the body. Precipitants include non steroidal anti-inflammatories, paracetamol and antibiotics81. Rarely a fixed drug eruption can occur when the sexual partner has taken the drug and it is assumed the toxic component of the drug is passed on through vaginal fluid82. Clinical Features Appearance: lesions are usually well demarcated and erythematous, but can be bullous with subsequent ulceration. As the inflammation settles there may be post-inflammatory hyperpigmentation. Diagnosis History: a drug history is essential. Re-challenge: This can confirm the diagnosis but can precipitate more severe reactions and should only be done with fully informed consent of the patient. Biopsy: Hydropic degeneration of the basal layer and epidermal detachment and necrosis with pigmentary incontinence. Management Management is symptomatic and the lesions will settle without treatment when the precipitant is discontinued Topical steroids - e.g. mild to moderate strength twice daily until resolution.80(IV, C) Oral antihistamines (IV,C) Rarely systemic steroids may be required if the lesions are severe. Follow up Not required after resolution Patients should be advised to avoid the precipitant. Pre-malignant conditions These entities are rare but important. There are three principal clinical presentations of penile intraepithelial neoplasia (PeIN) - Erythroplasia of Queyrat, Bowens disease of the penis and Bowenoid papulosis; they are strongly associated with human papillomavirus infection and/or lichen sclerosus.4, 83,84,85,86 All may progress to frank squamous cell carcinoma (SCC), but the risk is much less in Bowenoid papulosis (~1%) than Bowens disease (~5%) and Erythroplasia of Queyrat (~10-40%)6, 86 . In all three conditions the risk is increased if there is concomitant immune-incompetence such as in HIV, in case of an organ transplant patient or in those treated with small molecule (e.g. azathioprine, cyclosporin, methotrexate, leflunamide) and biologic immunosuppressants. SCC presents as an asymmetrical, irregular tender or painful ulcer or nodule and may coexist with PeIN and lichen sclerosus. Clinical Features4, 6, 53, 85, 86 Most lesions are located on the prepuce (45%), followed by the glans (38%) and shaft (3%).85 Erythroplasia of Queyrat (PeIN of the balanopreputial epithelium) Typical appearance: red, velvety, well-circumscribed area on the glans or visceral prepuce of the uncircumcised penis. Bowens disease (PeIN of keratinised, hair-bearing, skin) Typical appearance: scaly, discrete, erythematous patches or plaques. Bowenoid papulosis Typical appearance: clinically very similar to genital warts. Lesions range from discrete papules to plaques that are often grouped and pigmented or erythematous. Patients are usually younger than those with Bowens disease or Erythroplasia of Queyrat. Diagnosis Biopsy: essential histology shows penile intraepithelial neoplasia differentiated type (lichen sclerosus-associated) or undifferentiated (HPV-associated)85,87 Management (III, B - IV,C) 4,6, 5, 53, 85, 88, 89, 90 Patients with suspected penis cancer or pre-cancer should be discussed at a supra-regional MDT in the UK and are best managed by specialists in dermatology and urology/andrology. A combined, sequential approach is often needed. The approach should reflect individual clinical circumstances (age, circumcision status, site/sites, comorbidities, concomitant immunosuppression) and the pathogenesis (HPV and/or lichen sclerosus) and histology (differentiated or undifferentiated type). Topical medical91,92 Imiquimod 5%96 Fluorouracil cream 5%90 Fluorouracil 0.5% / salicylic acid 10%combination Podophyllotoxin 0.5% Surgical/ablative (aims are tissue conservation)93,94 Cryotherapy Photodynamic therapy Laser109, 110,111 Surgical excision (local excision is usually adequate and effective). Mohs micrographic surgery Mandatory circumcision for balanopreputial disease, especially for uncircumcised high-risk scenarios (eg HIV, transplant recipient etc) Glans-resurfacing (generally, if topical treatments have failed)112 Adjunctive Polyvalent HPV vaccination34 Smoking cessation Follow up Usually mandatory because of the risks of field change and recurrence; up to one third of patients may harbour (micro) invasive disease. Optimum length of follow up is uncertain. Circumcised patients with Bowenoid papulosis or PeIN confined to the prepuce might be discharged. Circumcision is usually mandatory because of the risk of recurrence, although optimum length of follow up is uncertain. In one study ~20% recurred after 5 years.94 Tuition in long-term self-examination if discharged. Bowenoid papulosis may remit spontaneously Other skin conditions A range of other skin conditions may affect the glans penis and genitalia. These include erythema multiforme and immuno-bullous disorders, including pemphigus, dermatitis artefacta and the very rare extramammary Pagets disease. 1, 4, 95 A dermatologists opinion should be sought for diagnosis and management of these conditions. Proposed review date: September 2025 Acknowledgements: None Funding Acknowledgement: This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors. List of contributing organisations IUSTI Europe European Academy of Dermatology and Venereology (EADV) European Dermatology Forum (EDF) European Society of Clinical Microbiology and Infectious Diseases (ESCMID) Union of European Medical Specialists (UEMS) European Centre for Disease Prevention and Control (ECDC) European Office of the World Health Organisation (WHO-Europe) References. Pearce J, Fernando I. The value of a multi-specialty service, including genitourinary medicine, dermatology and urology input, in the management of male genital dermatoses.Int J STD AIDS. 2015;26(10): 716-22. Morris BJ, Krieger JN. Penile Inflammatory Skin Disorders and the Preventive Role of Circumcision.Int J Prev Med. 2017;8:32. Edwards S, Bunker C. Chapter 7: Other conditions affecting the male genitalia. In: Rogstad K Ed. ABC of Sexually Transmitted Infections. 6th ed. Oxford: Wiley-Blackwell, 2011; 35-41. Bunker CB. Male Genital Skin Disease. E-book: Bruce Shrink, 2019 Chan I, Hawkins D, Bunker CB. 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Appendix 1 Search Strategy Evidence for this guideline has been provided by undertaking a search for English language articles published up to May 2020 from the following sources: Medline/Pubmed and Embase, the Cochrane Library (including the Cochrane Database of Systematic Reviews, Database of Abstracts and Reviews of Effects and Cochrane Central Register of Controlled Trials), British Association for Sexual Health and HIV (BASHH) and British Association of Dermatologists (BAD) guidelines (including the previous European guideline for the management of balanitis 2014, and the UK National guideline for the management of balanitis 2008), and the Naional I>NOfg~ 6 > ?   , ǹzpccZQhEahd^JhEah^"^JhEah^"OJQJ^Jhx\OJQJ^Jh(>*OJQJ^JhF>*OJQJ^JhFh'}>*OJQJ^JhF>*OJQJ^JhFhNvj>*H*OJQJ^JhFhNvj>*OJQJ^J&h:hx\5>*CJOJQJ^JaJ hNvj5>*CJOJQJ^JaJ&h:hNvj5>*CJOJQJ^JaJ>?  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Other relevant guidelines were identified on Google or produced by the US Centres for Disease Control. A further search of the Cochrane databases and National Institute for Health and Clinical Excellence guidelines were undertaken up to May 2020. Search terms included balanitis, balanoposthitis and all the specific aetiologies as listed in the introduction. This guideline is based on the 2014 European guideline for the management of balanitis with reference to UK National guideline for the management of balanitis 2008. Appendix 2 Levels of evidence and grading of recommendations Levels of Evidence Ia Evidence obtained from meta-analysis of randomised controlled trials. Ib Evidence obtained from at least one randomised controlled trial. IIa Evidence obtained from at least one well designed study without randomisation. IIb Evidence obtained from at least one other type of well designed quasi-experimental study. III Evidence obtained from well designed non-experimental descriptive studies such as comparative studies, correlation studies, and case control studies. IV Evidence obtained from expert committee reports or opinions and/or clinical experience of respected authorities. Grading of Recommendations A (Evidence levels Ia, Ib) Requires at least one randomised control trial as part of the body of literature of overall good quality and consistency addressing the specific recommendation. B (Evidence levels IIa, IIb, III) Requires availability of well conducted clinical studies but no randomised clinical trials on the topic of recommendation. C (Evidence IV) Requires evidence from expert committee reports or opinions and/or clinical experience of respected authorities. Indicates absence of directly applicable studies of good quality. Appendix 3 Declaration of Interests: Professor Bunker is the owner of Bruce Shrink Ltd the publishing company of his book Male Genital Skin Disease Appendix 4Composition of the editorial board Dr Keith Radcliffe, UK Editor-in-Chief Dr Marti Vall-Mayans, Spain (appointed 2015) Dr Andy Winter, UK (app. 2014) Dr Deniz Gkengin, Turkey (app. 2014) Dr Marco Cusini, Italy (app. 2010) Prof Mikhail Gomberg, Russia (app. 2010) Dr Jorgen Skov Jensen, Denmark (app. 2006) Dr Raj Patel, UK (app. 2006) Prof Jonathan Ross, UK (app. 2006) Dr Jackie Sherrard, UK (app. 2009) Dr Magnus Unemo, Sweden (app. 2009) Dr Willem van der Meijden, Netherlands (app. 2006) Prof Norbert Brockmeyer, Germany (app. 2017) Prof Gilbert Donders, Belgium - ISIDOG representative (app. 2012) Prof Mario Poljak, Slovenia ESCMID representative, (app. 2013) Dr Gianfranco Spiteri, Malta ECDC representative, (app. 2013) Prof George-Sorin Tiplica, Romania - EADV representative, (app. 2012) Dr Michel Janier, France UEMS representative (app. 2014) Dr Ricardo Werner, Germany - EDF representative (app. 2019) 9;<=>?J|}rjXY&'@ABƽ{shhphp^JaJhp^JaJhph#7I^JaJhph#7I>*^JaJh#7I>*^JaJ!hhB*OJQJ^JphhhhOJQJ^Jh>*^JaJh:h&b>*^Jh:h&b>*OJQJ^Jh&b>*OJQJ^JhGs>*OJQJ^Jh>*OJQJ^J"i=>?J|}rjXY'd^`gdixdgdix0d^`0gdixdgdix d^gdix'B 9X~5X|_ \ d7$8$H$gdp 7$8$H$gdpdgdixdgdix "dgdp 9X~5X|_ [\ȳ)hphfN|B*CJ^JaJnH phtH "hpCJOJQJ^JaJnH tH hDhoD>*CJ^JaJ h^">*^J hphl>*B*^JaJph.:pEa. 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