Management of penile dermatoses

References

• Moses S, Bailey RC, Ronald AR. Male circumcision: assessment of health benefits and risks. Sex Transm. Infect.74, 368–373 (1998).
   PubMed Web of Science ®Google Scholar
• Bunker CB. Male Genital Dermatology. Saunders, London, UK (2004).
   Google Scholar
• Singh-Grewal D, Macdessi J, Craig J. Circumcision for the prevention of urinary tract infection in boys: a systematic review of randomised trials and observational studies. Arch. Dis. Child.90, 853–858 (2005).
   PubMed Web of Science ®Google Scholar
• Van Howe RS. Effect of confounding in the association between circumcision status and urinary tract infection. J. Infect.51, 59–68 (2005).
   PubMed Web of Science ®Google Scholar
• O’Farrell N, Egger M. Circumcision in men and the prevention of HIV infection: a ‘meta-analysis’ revisited. Int. J. STD AIDS11, 137–142 (2000).
   PubMed Web of Science ®Google Scholar
• Bailey RC, Plummer FA, Moses S. Male circumcision and HIV prevention: current knowledge and future research directions. Lancet Infect. Dis.1, 223–231 (2001).
   PubMedGoogle Scholar
• Siegfried N, Muller M, Volmink J et al. Male circumcision for prevention of heterosexual acquisition of HIV in men. Cochrane Database Syst. Rev.3, CD003362 (2003).
   Google Scholar
• Inungu J, Malone Beach E, Betts J. Male circumcision and the risk of HIV infection. AIDS Read.15(3), 130–131 (2005).
   PubMedGoogle Scholar
• Auvert B, Taljaard D, Lagarde E, Sobngwi-Tambekou J, Sitta R, Puren A. Randomized, controlled intervention trial of male circumcision for reduction of HIV infection risk: the ANRS 1265 Trial. PLoS Med.2(11), E298 (2005).
   PubMed Web of Science ®Google Scholar
• Mallon E, Hawkins D, Dinneen M et al. Circumcision and genital dermatoses. Arch. Dermatol.136, 350–354 (2000).
   PubMed Web of Science ®Google Scholar
• Whitfield H. Circumcision. BJU Int.83(Suppl.1) 1–113 (1999).
   Google Scholar
• Alanis MC, Lucidii RS. Neonatal circumcision: a review of the world’s oldest and most controversial operation. Obstet. Gynaecol. Surv.59(5), 379–395 (2004).
   PubMed Web of Science ®Google Scholar
• Hutcheson JC. Male neonatal circumcision: indications, controversies and complications. Urol. Clin. N. Am.31, 461–467 (2004).
   PubMedGoogle Scholar
• Benatar M, Benatar D. Between prophylaxis and child abuse: the ethics of neonatal male circumcision. Am. J. Bioeth.3, 35–48 (2003).
   PubMed Web of Science ®Google Scholar
• Porter WM, Bunker CB. The dysfunctional foreskin. Int. J. STD AIDS12, 216–220 (2001).
   Google Scholar
• Mallon E, Ross JS, Hawkins DA, Dinneen M, Francis N, Bunker CB. Biopsy of male genital dermatoses. Genitour. Med.73, 421 (2004).
   Google Scholar
• Zoon JJ. Verenigingsverslagen. Nederl. Tijdschr. Geneeskd.94, 1528–1530 (1950).
   PubMedGoogle Scholar
• Zoon JJ. Balanoposthite chronique circonscrite benigne a plasmocytes. Dermatologica105, 1–7 (1952).
   PubMedGoogle Scholar
• Davis J, Shapiro L, Baral J. Vulvitis circumscripta plasmacellularis. J. Am. Acad. Dermatol.8, 413–416 (1983).
   PubMed Web of Science ®Google Scholar
• Woodruff JD, Sussman J, Shakfeh S. Vulvitis circumscripta plasma cellularis. J. Reprod. Med.34, 369–372 (1989).
   PubMedGoogle Scholar
• Baughman RD, Berger P, Pringle WM. Plasma cell cheilitis. Arch. Dermatol.110, 725–726 (1974).
   PubMedGoogle Scholar
• White JW Jr, Olsen KD, Banks PM. Plasma cell orificial mucositis. Arch. Dermatol.122, 1321–1324 (1986).
   PubMedGoogle Scholar
• Yoganathan S, Bohl TG, Mason G. Plasma cell balanitis and vulvitis (of Zoon). J. Reprod. Med.39, 939–944 (1994).
   PubMed Web of Science ®Google Scholar
• Altmeyer P, Kastner U, Luther H. Die Balanitis? Balanoposthitis chronica circumscripta benigna plasmacellularis-Entitat oder Fiktion? [Balanitis/balanoposthitis chronica circumscripta benignaplasmacellularis-entity or fiction]? Hautarzt49, 552–555 (1998).
   PubMedGoogle Scholar
• -Cascajo C. Balanitis of Zoon: a clinicopathologic study of 45 cases. Am. J. Dermatopathol.24, 459–467 (2002).
   PubMedGoogle Scholar
• Kiene P, Folster-Holst R. No evidence of human papillomavirus infection in balanitis circumscripta plasmacellularis Zoon. Acta Derm. Venereol.75, 496–497 (1995).
   PubMedGoogle Scholar
• Kuniyuki S, Asada T, Yasumoto R. A case of vulvitis circumscripta plasmacellularis positive for herpes simplex Type II antigen. Clin. Exp. Dermatol.23, 230–231 (1998).
   PubMedGoogle Scholar
• Toonstra J, van Wichen DF. Immunohistochemical characterization of plasma cells in Zoon’s balanoposthitis and (pre) malignant skin lesions. Dermatologica172, 77–81 (1986).
   PubMedGoogle Scholar
• Nishimura M, Matsuda T, Muto M, Hori Y. Balanitis of Zoon. Int. J. Dermatol.29, 421–423 (1998).
   Google Scholar
• Farrell AM, Francis N, Bunker CB. Zoon’s balanitis: an immunohistochemical study. Br. J. Dermatol.135(Suppl. 47), 57 (1996).
   Google Scholar
• Kumar B, Sharma R, Rajagopalan M, Radotra BD. Plasma cell balanitis: clinical and histopathological features–response to circumcision. Genitourin. Med.71, 32–34 (1996).
   Google Scholar
• Kossard S, Shumack S. Lichen aureus of the glans penis as an expression of Zoon’s balanitis. J. Am. Acad. Dermatol.21, 804–806 (1998).
   Google Scholar
• Bureau Y, Barriere H, Evin YP. Les erythroplasies benignes a plasmocytes. Ann. Dermatol. Syphilig.89, 271–284 (1962).
   PubMedGoogle Scholar
• Davis-Daneshfar A, Trueb RM. Bowen’s disease of the glans penis (erythroplasia of Queyrat) in plasma cell balanitis. Cutis65, 395–398 (2000).
   PubMedGoogle Scholar
• Dupre A, Bonafe J-L, Lassere J et al. Lesions bourgeonnantes pruputiales a plasmocytes: variante anatomo-clinique de la balano-posthite chronique circonscrite benigne de Zoon. Bulletin de la Societe Francaise Dermatologie et Syphiligraphie83, 62–63 (1976).
   Google Scholar
• Jonquieres EDL. Balanitis pseudoeritroplasicas. Archivos Argentinos de Dermatologica21, 85–95 (1971).
   Google Scholar
• Porter WM, Hawkins DA, Dinneen M, Bunker CB. Zoon’s balanitis and carcinoma of the penis. Int. J. STD AIDS11, 484–485 (2002).
   Google Scholar
• Sonnex TS, Dawber RPR, Ryan TJ, Ralfs IG. Zoon’s (plasma-cell) balanitis: treatment by circumcision. Br. J. Dermatol.106, 585–588 (1982).
   PubMedGoogle Scholar
• Tang A, David N, Horton LW. Plasma cell balanitis of Zoon: response to Trimovate cream. Int. J. STD AIDS12, 75–78 (2001).
   PubMedGoogle Scholar
• Santos-Juanes J, Sanchez del Rio J, Galache C, Soto J. Topical tacrolimus: an effective therapy for Zoon balanitis. Arch. Dermatol.140, 1538–1539 (2004).
   PubMed Web of Science ®Google Scholar
• Hernandez-Machin B, Hernando LB, Marrero OB, Hernandez B. Plasma cell balanitis of Zoon treated successfully with topical tacrolimus. Clin. Exp. Dermatol.30, 588–589 (2005).
   PubMedGoogle Scholar
• Albertini JG, Holck DE, Farley MF. Zoon’s balanitis treated with Erbium: YAG laser ablation. Lasers Surg. Med.30, 123–126 (2002).
   PubMedGoogle Scholar
• Retamar RA, Kien MC, Chouela EN. Zoon’s balanitis: presentation of 15 patients, five treated with carbon dioxide laser. Int. J. Dermatol.42, 305–307 (2003).
   PubMedGoogle Scholar
• Itin PH, Hirsbrunner P, Buchner S. Lichen planus: an unusual cause of phimosis. Acta Dermato-Venereologica 72(1), 41–42, (1992).
   PubMedGoogle Scholar
• Aste N, Pau M, Ferreli C, Biggio P. Lichen planus in a child requiring circumcision. Pediatr. Dermatol.14(2), 129–130 (1997).
   PubMedGoogle Scholar
• Cribier B, Ndiaye I, Grosshans E. Peno-gingival syndrome. A male equivalent of vulvo-vagino-gingival syndrome. Revue de Stomatologie et de Chirurgie Maxillo-Faciale94(3), 148–151 (1992).
   Google Scholar
• Hahn JM, Meisler DM, Lowder CY, Tung RC, Camisa C. Cicatrizing conjunctivitis associated with paraneoplastic lichen planus. Am. J. Ophthalmol.129(1) 98–99 (2000).
   PubMed Web of Science ®Google Scholar
• Worheide J, Bonsmann G, Kolde G, Hamm H. Plattenepithyelkarzinom auf dem Boden eines lichen ruber hypertrophicus an der glans penis. Der Hautarzt42(2), 112–115 (1991).
   PubMedGoogle Scholar
• Leal-Khouri S, Hruza GJ. Squamous cell carcinoma developing within lichen planus of the penis. Treatment with Mohs micrographic surgery. J. Dermatol. Surg. Oncol.20(4), 272–276 (1994).
   PubMedGoogle Scholar
• Jemec GBE, Baadsgaard O. Effect of cyclosporin on genital psoriasis and lichen planus. A randomised trial of simple excision of non-specific hypertrophied anal papillae versus expectant management in patients with chronic pruritus ani. Ann. R. Col. Surg. (England)70, 348–349 (1988).
   PubMedGoogle Scholar
• Schmitt EC, Pigatto PD, Boneschi V, Bigardi AS, Finzi AF. Erosiver lichen planus der glans penis. Der Hautarzt44(1), 43–45 (1993).
   PubMedGoogle Scholar
• Kirby B, Whitehurst C, Moore JV, Yates VM. Treatment of lichen planus of the penis with photodynamic therapy. Br. J. Dermatol.141(4), 765–766 (1999).
   PubMedGoogle Scholar
• Porter WM, Dinneen M, Hawkins DA, Bunker CB. Erosive penile lichen planus responding to circumcision. JEADV15, 266–268 (2001).
   Google Scholar
• Perceau G, Derancourt C, Clavel C et al. Lichen sclerosus is frequently present in penile squamous cell carcinoma but is not always associated with oncogenic human papillomavirus. Br. J. Dermatol.148, 934–938 (2003).
   PubMedGoogle Scholar
• Velazquez EF, Cubilla AL. Lichen sclerosus in 68 patients with squamous cell carcinoma of the penis: frequent atypias and correlation with special carcinoma variants suggests a precancerous role. Am. J. Surg. Pathol.27, 1148–1153 (2003).
   Google Scholar
• Ritchie AWS, Foster PW, Fowler S. Penile cancer in the UK: clinical presentation and outcome in 1998/99. BJU Int.94, 1248–1252 (2004).
   PubMedGoogle Scholar
• Powell JJ, Wojnarowska F. Lichen sclerosus. Lancet353, 1777–1783 (1999).
   PubMed Web of Science ®Google Scholar
• English JC III, King DH, Foley JP. Penile shaft hypopigmentation: lichen sclerosus occurring after the initiation of alprostadil intracavernous injections for erectile dysfunction. J. Am. Acad. Dermatol.39, 801–803 (1998).
   PubMedGoogle Scholar
• Mattioli G, Repetto P, Carlini C, Granata C, Gambini C, Jasonni V. Lichen sclerosus et atrophicus in children with phimosis and hypospadias. Pediatr. Surg. Int.18, 273–275 (2002).
   PubMedGoogle Scholar
• Weigand DA. Microscopic features of lichen sclerosus et atrophicus in acrochordons: a clue to the cause of lichen sclerosus et atrophicus? J. Am. Acad. Dermatol.28, 751–754 (1993).
   PubMedGoogle Scholar
• Wallace HJ. Lichen sclerosus et atrophicus. Trans. St John’s Dermatol. Soc.57, 9–30 (1971).
   PubMedGoogle Scholar
• Goolamali SK, Barnes EN, Irvine WJ et al. Organ-specific antibodies in patients with lichen sclerosus. BMJ iv: 78–79 (1974).
   PubMedGoogle Scholar
• Harrington Cl, Dunsmore IR. An investigation into the incidence of autoimmune disorders in patients with lichen sclerosus et atrophicus. Br. J. Dermatol.104, 563–566 (1981).
   PubMed Web of Science ®Google Scholar
• Meyrick Thomas RH, Ridley CM, Black MM. The association of lichen sclerosus et atrophicus and autoimmune-related disease in males. Br. J. Dermatol.109, 661–664 (1983).
   PubMedGoogle Scholar
• Tremaine RDL, Miller RAW. Lichen sclerosus et atrophicus. Int. J. Dermatol.28, 10–16 (1989).
   PubMedGoogle Scholar
• Vaccaro M, Guarneri F, Borgia F, Cannavo SP, Benvenga S. Association of lichen sclerosus and autoimmune thyroiditis: possible role of borrelia burgdorferi? Thyroid12, 1147–1148 (2002).
   PubMed Web of Science ®Google Scholar
• Azurdia RM, Luzzi GA, Byren I et al. Lichen sclerosus in adult men: a study of HLA associations and susceptibility to autoimmune disease. Br. J. Dermatol.140, 79–83 (1999).
   PubMed Web of Science ®Google Scholar
• Senturk N, Aydin F, Birinci A et al. Coexistence of HLA-B*08 and HLA-B*18 in four siblings with lichen sclerosus. Dermatology208, 64–66 (2004).
   PubMed Web of Science ®Google Scholar
• Hinchliffe SA, Ciftci AO, Rickwood AMK et al. Compostion of the inflammatory infiltrate in pediatric penile lichen sclerosus and atrophicus (balanitis xerotica obliterans). Pediatr. Pathol.14, 223–233 (1994).
   PubMed Web of Science ®Google Scholar
• Farrell AM, Marren P, Dean D, Wojnarowska F. Lichen sclerosus: evidence that immunological changes occur at all levels of the skin. Br. J. Dermatol.140, 1087–1092 (1999).
   PubMed Web of Science ®Google Scholar
• Regauer S, Liegl B, Reich O, Beham-Schmid C. Vasculitis in lichen sclerosus: an under recognized feature? Histopathology45, 237–244 (1995).
   Google Scholar
• Regauer S, Reich O, Beham-Schmid C. Monoclonal γ-T-cell receptor rearrangement in vulvar sclerosus and squamous cell carcinoma. Am. J. Pathol.160, 1035–1045 (2002).
   PubMed Web of Science ®Google Scholar
• Tchorzewski H, Rotsztejn H, Banasik M, Lewkowicz P, Glowacka E. The involvement of immunoregulatory T-cells in the pathogenesis of lichen sclerosus. Med. Sci. Monit.11, CR39–CR43 (2005).
   Google Scholar
• Regauer S. Immune dysregulation in lichen sclerosus. Eur. J. Cell Biol.84, 273–277 (2005).
   PubMed Web of Science ®Google Scholar
• Aberer E, Neumann R, Lubec G. Acrodermatitis chronica atrophicans in association with lichen sclerosus et atrophicans: tubulo-interstitial nephritis and urinary excretion of spirochete-like organisms. Acta Derm. Venereol. (Stockh.)67, 62–91 (1987).
   PubMedGoogle Scholar
• Schempp C, Bocklage H, Lange R, Kölmel HW, Orfanos CE. Further evidence for borrelia burgdorferi infection in morphea and lichen sclerosus et atrophicus confirmed by DNA amplification. J. Invest. Dermatol.100, 717–720 (1993).
   PubMed Web of Science ®Google Scholar
• Foldes-Papp Z, Reich O, Demel U, Tilz GP. Lack of specific immunological disease pattern in vulvar lichen sclerosus. Exp. Mol. Pathol.79, 176–185 (2005).
   PubMedGoogle Scholar
• Drut RM, Gomez MA, Drut R, Lojo MM. Human papillomavirus is present in some cases of childhood penile lichen sclerosus: an in situ hybridization and SP-PCR study. Pediatr. Dermatol.15, 85–90 (1998).
   PubMed Web of Science ®Google Scholar
• Farrell AM, Millard PR, Schomberg KH, Wojnarowska F. An infective aetiology for lichen sclerosus re-addressed. Clin. Exp. Dermatol.24, 479–483 (1999).
   PubMed Web of Science ®Google Scholar
• Oyama N, Chan I, Neill SM et al. Autoantibodies to extracellular matrix protein 1 in lichen sclerosus. Lancet362(9378), 118–123 (2003).
   PubMedGoogle Scholar
• Edmonds EV, Chan I, Pyama N et al. Autoantibodies to extracellular matrix protein 1 in male genital lichen sclerosus. J. Invest. Dermatol.124(Suppl.) (2005).
   Google Scholar
• Sander CS, Ali I, Dean D, Thiele JJ, Wojnarowska F. Oxidative stress is implicated in the pathogenesis of lichen sclerosus. Br. J. Dermatol.151, 627–635 (2004).
   PubMed Web of Science ®Google Scholar
• Chalmers RJG, Burton PA, Bennett RF, Goring CC, Smith PJB. Lichen sclerosus et atrpohicus. Arch. Dermatol.120, 1025–1027 (1984).
   PubMedGoogle Scholar
• Rickwood AM, Hemalatha V, Batcup G, Spitz L. Phimosis in boys. Br. J. Urol.52, 147–150 (1980).
   PubMedGoogle Scholar
• Ridley CM. Genital lichen sclerosus (lichen sclerosus et atrophicus) in childhood and adolescence. J. R. Soc. Med.86, 69–75 (1993).
   PubMedGoogle Scholar
• Meuli M, Brinker J, Hanimann B, Sacher P. Lichen sclerosus and atrophicus causing phimosis in boys: a prospective study with 5-year follow-up after complete circumcision. J. Urol.152, 987–989 (1994).
   PubMed Web of Science ®Google Scholar
• Clemmensen OJ, Krogh J, Petri M. The histologic spectrum of prepuces from patients with phimosis. Am. J. Dermatopathol.10, 104–108 (1988).
   PubMedGoogle Scholar
• Aynaud O, Piron D, Casanova JM. Incidence of preputial lichen sclerosus in adults: histologic study of circumcision specimens. J. Am. Acad. Dermatol.41, 923–926 (1999).
   PubMed Web of Science ®Google Scholar
• Ridley CM, Neill SM. Circumcision. BMJ306(6877), 583–584 (1993).
   PubMedGoogle Scholar
• Barbagli G, Palminteri E, Balo S et al. Lichen sclerosus of the male genitalia and urethral stricture diseases. Urol. Int.73, 1–5 (2004).
   PubMed Web of Science ®Google Scholar
• Jenny C, Kirby P, Fuquay D. Genital lichen sclerosus mistaken for child sexual abuse. Pediatrics83, 597–599 (1989).
   PubMedGoogle Scholar
• Loening-Baucke V. Lichen sclerosus and atrophicus in children. Am. J. Dis. Child.145, 1058–1061 (1991).
   PubMedGoogle Scholar
• Al-Khenaizan S, Almuneef M, Kentab O. Lichen sclerosus mistaken for child sexual abuse. Int. J. Dermatol.44, 317–320 (2005).
   PubMedGoogle Scholar
• Berth-Jones J, Graham-Brown RA, Burns DA. Lichen sclerosus. Arch. Dis. Child.64, 1204–1206 (1989).
   PubMedGoogle Scholar
• Harrington CI. Lichen sclerosus. Arch. Dis. Child.65, 335 (1990).
   PubMedGoogle Scholar
• Tasker GL, Wojnarowska F. Lichen sclerosus. Clin. Exp. Dermatol.28, 128–133 (2003).
   PubMedGoogle Scholar
• Neill SM, Tatnall FM, Cox NH. British Association of Dermatologists. Guidelines for the management of lichen sclerosus. Br. J. Dermatol.147, 640–649 (2002).
   PubMed Web of Science ®Google Scholar
• Dahlman-Ghozlan K, Hedblad MA, von Krogh G. Penile lichen sclerosus and atrophicus treated with clobetasol dipropionate 0.05% cream: a retrospective clinical and histopathological study. J. Am. Acad. Dermatol.40, 451–457 (1999).
   PubMedGoogle Scholar
• Lindhagen T. Topical clobetasol propionate compared with placebo in the treatment of unretractable foreskin. Eur. J. Surg.162, 969–972 (1996).
   PubMedGoogle Scholar
• Jorgensen ET, Svensson A. Problems with the penis and prepuce in children. Lichen sclerosus should be treated with corticosteroids to reduce need for surgery. BMJ313, 692 (1996).
   PubMedGoogle Scholar
• Pasieczny TAH. The treatment of balanitis xerotica obliterans with testosterone propionate ointment. Acta. Dermato-Venereologica57, 275–277 (1977).
   PubMedGoogle Scholar
• Heise H, Flegel H, Helmke R. Treatment of lichen sclerosus and atrophicus with testosterone propionate ointment. Dermatol. Monatssch.170, 135–138 (1984).
   PubMedGoogle Scholar
• Skierlo P, Heise H. Testosterone propionate ointment – a therapeutic trial in lichen sclerosus et atrophicus. Hautarzt38, 295–297 (1987).
   PubMedGoogle Scholar
• Virgili A, Corazza M, Bianchi A, Mollica G, Califano A. Open study of topical 0.025% tretinoin in the treatment of vulval lichen sclerosus. One year of therapy. J. Reprod. Med.40, 614–618 (1995).
   PubMed Web of Science ®Google Scholar
• Kaya G, Saurat JH. Restored epidermal CD44 expression in lichen sclerosus and atrophicus and clinical improvement with topical application of retinaldehyde. Br. J. Dermatol. 152, 570–572 (2005).
   PubMed Web of Science ®Google Scholar
• Reichrath J, Reinhold U, Tilgen W. Treatment of genito-anal lesions in inflammatory skin diseases with PUVA cream photochemotherapy: an open pilot study in 12 patients. Dermatology. 205, 245–248 (2002).
   PubMed Web of Science ®Google Scholar
• Bohm M, Frieling U, Luger TA, Bonsmann G. Successful treatment of anogenital lichen sclerosus with topical tacrolimus.Arch. Dermatol.139, 922–924 (2003).
   PubMedGoogle Scholar
• Kunstfeld R, Kirnbauer R, Stingl G, Karlhofer FM. Successful treatment of vulvar lichen sclerosus with topical tacrolimus. Arch. Dermatol.39, 850–852 (2003).
   Google Scholar
• Assmann T, Becker-Wegerich P, Grewe M, Megahed M, Ruzicka T. Tacrolimus ointment for the treatment of vulvar lichen sclerosus. J. Am. Acad. Dermatol.48, 935–937 (2003).
   PubMed Web of Science ®Google Scholar
• Pandher BS, Rustin MH, Kaisary AV. Treatment of balanitis xerotica obliterans with topical tacrolimus. J. Urol.17, 923923 (2003).
   Google Scholar
• Marini A, Blecken S, Ruzicka T, Hengge UR. Lichen sclerosus. New aspects of pathogenesis and treatment. Hautarzt.56, 550–555 (2005).
   PubMedGoogle Scholar
• Bunker CB, Neill S, Staughton RCD. Topical tacrolimus, genital lichen sclerosus and risk of squamous cell carcinoma. Arch. Dermatol.140, 1169 (2004).
   PubMedGoogle Scholar
• Langeland T, Engh V. Topical use of tacrolimus and squamous cell carcinoma on the penis. Br. J. Dermatol.152, 176–198 (2005).
   Google Scholar
• Shelley WB, Shelley ED, Grunenwald MA et al. Long-term antibiotic therapy for balanitis xerotica obliterans. J. Am. Acad. Dermatol.40, 69–72 (1999).
   PubMedGoogle Scholar
• Parsad D, Saini R. Oral stanozolol in lichen sclerosus et atrophicus. J. Am. Acad. Dermatol.38, 278–279 (1998).
   PubMedGoogle Scholar
• Ronger S, Viallard AM, Meunier-Mure F, Chouvet B, Balme B, Thomas L. Oral calcitriol: a new therapeutic agent in cutaneous lichen sclerosus. J. Drugs Dermatol.2, 23–28 (2003).
   PubMedGoogle Scholar
• Neuhofer J, Fritsch P. Treatment of localized scleroderma and lichen sclerosus with etretinate. Acta Derm. Venereol.64, 171–174 (1984).
   PubMed Web of Science ®Google Scholar
• Yokota M, Mizuno N. A case of lichen sclerosus et atrophicus of the vulva effectively treated with oral etretinate. J. Dermatol.15, 330–333 (1988).
   PubMedGoogle Scholar
• Bousema MT, Romppanen U, Gieger JM et al. Acitretin in the treatment of severe lichen sclerosus et atrophicus of the vulva: a double-blind, placebo-controlled study. J. Am. Acad. Dermatol.30, 225–231 (1994).
   PubMedGoogle Scholar
• Meyrick Thomas RH, Ridley CM, Black MM. Clinical features and therapy of lichen sclerosus et atrophicus affecting males. Clin. Exp. Dermatol.12, 126–128 (1987).
   PubMedGoogle Scholar
• Happle R. Chirurgische Behandlung des Lichen sclerosus et atrophicus penis. [Surgical treatment of penile lichen sclerosus et atrophicus]. Dermatol. Monatssch.159, 975–977 (1973).
   PubMedGoogle Scholar
• Campus GV, Ena P, Scuderi N. Surgical treatment of balanitis xerotica obliterans. Plast. Reconstr. Surg.73, 652–657 (1984).
   PubMedGoogle Scholar
• Peterson AC, Palminteri E, Lazzeri M, Guanzoni G, Barbagli G, Webster GD. Heroic measures may not always be justified in extensive urethral stricture due to lichen sclerosus (balanitis xerotica obliterans). Urology64, 565–568 (2004).
   PubMedGoogle Scholar
• Barbagli G, Palminteri E, Bracka A, Caparros Sariol J. Penile urethral reconstruction: concepts and concerns. Arch. Esp. Urol.56, 549–556 (2003).
   PubMedGoogle Scholar
• Lee SJ, Phillips SM. Recurrent lichen sclerosus et atrophicus in urethroplasties from multiple skin grafts. Br. J. Urol.74, 802–803 (1994).
   PubMedGoogle Scholar
• Aynaud O, Casanova JM, Tranbaloc P. CO2 laser for therapeutic circumcision in adults. Eur. Urol.28, 74–76 (1995).
   PubMed Web of Science ®Google Scholar
• Hrebinko RL. Circumferential laser vaporization for severe meatal stenosis secondary to balanitis xerotica obliterans. J. Urol.156, 1735–1736 (1996).
   PubMed Web of Science ®Google Scholar
• Kartamaa M, Reitamo S. Treatment of lichen sclerosus with carbon dioxide laser vaporization. Br. J. Dermatol.136, 356–359 (1997).
   PubMed Web of Science ®Google Scholar
• Ridley CM. Lichen sclerosus et atrophicus. Arch. Dermatol.123, 457–460 (1987).
   PubMedGoogle Scholar
• Schnitzler L, Sayag J, Sayag J et al. Epitheliome spino-cellulaire aign de la verge et lichen sclero-atrophique. Ann. Dermatol. Venereol.114, 979–981 (1987).
   PubMedGoogle Scholar
• Weber P, Rabinovitz H, Garland L. Verrucous carcinoma in penile lichen sclerosus et atrophicus. J. Dermatol. Surg. Oncol.13, 529–532 (1987).
   PubMedGoogle Scholar
• Campus GV, Alia F, Bosincu L. Squamous cell carcinoma and lichen sclerosus et atrophicus of the prepuce. Plast. Reconst. Surg.89, 962–964 (1992).
   PubMed Web of Science ®Google Scholar
• Simonart T, Noel JC, De Dobbeleer G, Simonart JM. Carcinoma of the glans penis arising 20 years after lichen sclerosus. Dermatology196, 337–338 (1998).
   PubMed Web of Science ®Google Scholar
• ParicioRubio JF, Revenga AF, Alfaro TJ, Ramirez GT. Squamous cell carcinoma of the penis arising on lichen sclerosus et atrophicus. J. Eur. Acad. Dermatovenereol.12, 153–156 (1999).
   PubMedGoogle Scholar
• Nasca MR, Innocenzi D, Micali G. Penile cancer among patients with genital lichen sclerosus. J. Am. Acad. Dermatol.41, 911–914 (1999).
   PubMed Web of Science ®Google Scholar
• Micali G, Nasca MR, Innocenzi D. Lichen sclerosus of the glans is significantly associated with penile carcinoma. Sex Transm. Infect.77, 226 (2001).
   PubMedGoogle Scholar
• Cubilla AL, Velazquez EF, Young RH. Pseudohyperplastic squamous cell carcinoma of the penis associated with lichen sclerosus. An extremely well-differentiated, non-verruciform neoplasm that preferentially affects the foreskin and is frequently misdiagnosed: a report of 10 cases of a distinctive clinicopathologic entity. Am. J. Surg. Pathol.28, 895–900 (2004).
   PubMedGoogle Scholar
• Pinto AP, Lin MC, Sheets EE, Muto MG, Crum CP. Allelic imbalance in lichen sclerosus, hyperplasia and intraepithelial neoplasia of the vulva. Gynecol. Oncol.77, 171–176 (2000).
   PubMedGoogle Scholar
• Maden C, Sherman KJ, Beckmann AM et al. History of circumcision, medical conditions, and sexual activity and the risk of penile cancer. J. Natl Cancer Inst.85, 19–24 (1993).
   PubMed Web of Science ®Google Scholar
• Holly EA, Palefsky JM. Factors related to risk of penile cancer: New evidence from a study in the Pacific northwest. J. Natl Cacer Inst.85, 2–3 (1993).
   PubMedGoogle Scholar
• Renaud-Vilmer C, Cavelier-Balloy B, Porcher R, Dubertret L. Vulvar lichen sclerosus: effect of long-term topical application of a potent steroid on the course of the disease. Arch. Dermatol.140, 709–712 (2004).
   PubMedGoogle Scholar
• Von Krogh G, Dahlman-Ghozlan K, Syrjanen S. Potential human papillomavirus reactivation following topical corticosteroid therapy of genital lichen sclerosus and erosive lichen planus. J. Eur. Acad. Dermatol. Venereol.16, 130–133 (2002).
   PubMedGoogle Scholar
• Bouyssou-Gauthier ML, Boulinguez S, Dumas JP, Bedane C, Bonnetblanc JM. Lichen sclereux genital masculin: etude de suivi. [Penile lichen sclerosus: follow-up study]. Ann. Dermatol. Venereol.126, 804–807 (1999).
   PubMedGoogle Scholar
• Liatsikos EN, Perimenis P, Dandinis K, Kaladelfou E, Barbalias G. Lichen sclerosus et atrophicus. Findings after complete circumcision. Scand. J. Urol. Nephrol.31, 453–456 (1997).
   PubMed Web of Science ®Google Scholar
• Hunt SJ, Francis N, Dinneen M, Hawkins D, Bunker CB. A retrospective study of 174 men with lichen sclerosus of the penis. Br. J. Dermatol.149(Suppl), 53–54 (2003).
   PubMedGoogle Scholar
• Yesudian PD, Sugunendran H, Bates CM, O’Mahony C. Lichen sclerosus. Int. J. STD AIDS16, 465–473 (2005).
   PubMed Web of Science ®Google Scholar
• Bunker CB. Diagnosis and management of penile pre-cancer: combined clinics and topical chemotherapy. In: The Effective Management of Urological Malignancies. Anderson J, Oliver RTD, Miles A (Eds). Aesculapius Medical Press, London, UK (2005).
   Google Scholar
• Edwards S. Balanitis and balanoposthitis: a review. Genitourin. Med.72, 155–159 (1996).
   PubMedGoogle Scholar
• English JC III, Laws RA, Keough GC, Wilde JL, Foley JP, Elston DM. Dermatoses of the glans penis and prepuce. J. Am. Acad. Dermatol.37, 1–24 (1997).
   PubMed Web of Science ®Google Scholar
• Fornasa CV, Calabro A, Miglietta A, Tarantello M, Biasinutto C, Peserico A. Mild balanoposthitis. Genitourin. Med.70, 345–346 (1994).
   PubMedGoogle Scholar
• Birley HDL, Walker MM, Luzzi GA et al. Features and management of recurrent balanitis; association with atopy and genital washing. Genitourinary Med.69, 400–403 (1993).
   PubMedGoogle Scholar
• Chopra R, Fisher RD, Fencel R. Phimosis and diabetes mellitus. J. Urol.127, 1101–1102 (1982).
   PubMedGoogle Scholar
• Alessi E, Coggi A, Gianotti R. Review of 120 biopsies performed on the balano-preputial sac. from Zoon’s balanitis to the concept of a wider spectrum of inflammatory non-cicatricial balanoposthitis. Dermatology208, 120–124 (2004).
   PubMedGoogle Scholar
• Edwards SK. European Branch of the International Union against Sexually Transmitted Infection and the European Office of the World Health Organization. European guideline for the management of balanoposthitis. Int. J. STD AIDS12, 68–72 (2001).
   PubMedGoogle Scholar
• Cotterill JA. A dermatological non-disease – a common and potentially fatal disturbance of cutaneous body image. Br. J. Dermatol.103(Suppl. 18), 13 (1980).
   Google Scholar
• Markos AR. The male genital skin burning syndrome (dysaesthetic peno/scroto-dynia). Int. J. STD AIDS13(4), 271–272 (2002).
   PubMedGoogle Scholar
• Parks AG, Porter NH, Hardcastle J. The syndrome of descending perineum. Proc. R. Soc. Med.59, 477–482 (1966).
   Google Scholar
• Lask D, Kimche D. Congenital polyp of the prostatic urethra. J. Urol.127(1), 134 (1982).
   PubMedGoogle Scholar
• Neill ME, Swash M. Chronic perianal pain: an unsolved problem. J. R. Soc. Med.75, 96–101 (1982).
   PubMedGoogle Scholar
• Wesselmann U, Burnett AL, Heinberg LJ. The urogenital and rectal pain syndromes. Pain73, 269–294 (1997).
   Google Scholar
• Fisher BK. The red scrotum syndrome. Cutis60, 139–141 (1997).
   PubMed Web of Science ®Google Scholar
• Feler CA, Whitworth LA, Fernandez J. Sacral neuromodulation for chronic pain conditions. Anesthesiol. Clin. N. Am.21, 785–795 (2003).
   PubMedGoogle Scholar
• Carter JE. A systematic history for the patient with chronic pelvic pain. JSLS3, 245–252 (1999).
   PubMedGoogle Scholar
• Morrissette DL, Goldstein MK, Raskin DB, Rowland DL. Finger and penile tactile sensitivity in sexually functional and dysfunctional diabetic men. Diabetologia42, 336–342 (1999).
   PubMedGoogle Scholar
• Romito S, Bottanelli M, Pellegrini M, Vicentini S, Rizzuto N, Bertolasi L. Botulinum toxin for the treatment of genital pain syndromes. Gynaecol. Obstet. Invest.58, 164–167 (2004).
   PubMedGoogle Scholar
• Cohen AD, Vander T, Medvendovsky E et al. Neuropathic scrotal pruritus: anogenital pruritus is a symptom of lumbosacral radiculopathy. J. Am. Acad. Dermatol. 52, 61–66 (2005).
   PubMed Web of Science ®Google Scholar
• Bunker CB, Bridgett CK, Depression and the skin. In: Depression and Physical Illness (Perspectives in Psychiatry). Robertson MM, Katona CLE (Eds), John Wiley and son Ltd, UK (1997).
   Google Scholar
• Pietrzak P, Watkin N. Modern management of penile cancer. In: The Effective Management of Urological Malignancies. Anderson J, Oliver RTD, Miles A (Eds). Aesculapius Medical Press, London, UK (2005).
   Google Scholar
• Hamid R, Chergill I, Arya M, Patel HR. Penile cancer: an overview. Hosp. Med.63, 718–721 (2002).
   PubMedGoogle Scholar
• Droller MJ. Carcinoma of the penis: an overview. Urol. Clin. N. Am.7, 783–784 (1980).
   PubMedGoogle Scholar
• Misra S, Chaturvedi A, Misra NC. Penile carcinoma: a challenge for the developing world. Lancet Oncol.5, 240–247 (2004).
   PubMed Web of Science ®Google Scholar
• Frisch M, Friis S, Kjaer SK, Melbye M. Falling incidence of penis cancer in an uncircumcised population (Denmark 1943–90). Br. Med. J. 311, 1471 (1995).
   PubMed Web of Science ®Google Scholar
• Markos AR. The management of penile intraepithelial neoplasia in genitourinary med. Int. J. STD AIDS14, 314–319 (2003).
   PubMedGoogle Scholar
• Graham JH, Helwig EB. Bowen’s disease and its relationship to internal malignancy. Arch. Dermatol.80, 133–159 (1959).
   Google Scholar
• Graham JH, Mazzanti GR, Helwig EB. Chemistry of Bowen’s disease: relationship to arsenic. J. Invest. Dermatol.37, 317–329 (1961).
   PubMed Web of Science ®Google Scholar
• Graham JH, Helwig EB. Erythroplasia of Queyrat: a clinicopathologic and histochemical study. Cancer32, 1396–1414 (1977).
   Google Scholar
• Gerber GS. Carcinoma in situ of the penis. J. Urol.151, 829–833 (1994).
   PubMed Web of Science ®Google Scholar
• Bowen JT. Precancerous dermatoses: a study of two cases of chronic atypical epithelial proliferation. J. Cut. Dis.30, 241–254 (1912).
   Google Scholar
• Reed DC. Erythroplasia of Queyrat: an unusual instance in a Negro patient involving the penis and progressing to invasive carcinoma. J. Kans. Med. Soc.57, 482–484 (1956).
   PubMedGoogle Scholar
• Milstein HG. Erythroplasia of Queyrat in a partially circumcised man. J. Am. Acad. Dermatol.10, 398 (1982).
   Google Scholar
• McAninch JW, Moore CA. Precancerous penile lesions in young men. J. Urol.104, 287–290 (1970).
   PubMedGoogle Scholar
• Yasuda M, Tamura A, Shinizu A, Takahashi A, Ishikawa O. Bowen’s disease involving the urethra. J. Dermatol.32, 210–213 (2005).
   PubMedGoogle Scholar
• Lloyd KM. Multicentric pigmented Bowen’s disease of the groin. Arch. Dermatol.101, 48–51 (1970).
   PubMedGoogle Scholar
• Wade TR, Kopf AW, Ackerman AB. Bowenoid papulosis of the genitalia. Arch. Dermatol.115, 306–308 (1979).
   PubMedGoogle Scholar
• Schwartz RA, Janniger CK. Bowenoid papulosis. J. Am. Acad. Dermatol.24, 261–263 (1991).
   PubMedGoogle Scholar
• Paget J. On disease of the mammary areola preceding carcinoma of the mammary gland. St Bartholomew’s Hospital Reports10, 87–89 (1874).
   Google Scholar
• Fournier A, Darier J. Epithelioma benin syphiloide de la verge (epitheliome papilllaire) Bulletin de la Societe Francaise Dermatologie et Syphigraphie4, 324 (1893).
   Google Scholar
• Morestin H. Deux cas de cancer du penis. Bulletin Societe Anatomie Paris5, 387 (1903).
   Google Scholar
• Queyrat L. Erythroplasie du gland. Bulletin de la Societe Francaise Dermatologie et Syphigraphie22, 378–382 (1911).
   Google Scholar
• Blau S, Hyman AB. Erythroplasic of Queyrat. Acta Derm. Venereol.35, 341–378 (1955).
   PubMedGoogle Scholar
• Cubilla AL, Meijer CJLM, Young RH. Morphological features of epithelial abnormalities and precancerous lesions of the penis. Scand. J. Urol. Nephrol.205(Suppl), 215–219 (2000).
   Google Scholar
• Cubilla AL, Velazquez EF, Young RH. Epithelial lesions associated with invasive penile squamous cell carcinoma: a pathologic study of 288 cases. Int. J. Surg. Pathol.12, 351–364 (2004).
   PubMed Web of Science ®Google Scholar
• Niederauer HH, Weindorf N, Schultz-Ehrenburg U. A case of giant condyloma acuminatum. On differential diagnosis of giant condylomas from Buschke-Lowenstein tumors and verrucous carcinoma. Hautarzt44, 795–799 (1993).
   PubMedGoogle Scholar
• Noel JC, Vandenbossche M, Peny MO at al. Verrucous carcinoma of the penis: importance of human papillomavirus typing for diagnosis and therapeutic decision. Eur. Urol.22, 83–85 (1992).
   PubMedGoogle Scholar
• Gonzalez-Lopez A, Esquivias JI, Miranda-Romero A, Massa CF, Tejerina JA. Buschke-Lowenstein tumor and immunity. Cutis59, 119–122 (1997).
   PubMedGoogle Scholar
• Anadolu R, Boyvat A, Calikoglu E, Gurler A. Buschke-Loewenstein tumour is not a low-grade carcinoma but a giant verucca. Acta. Derm. Venereol.79, 253–254 (1999).
   PubMedGoogle Scholar
• Haycox CL, Kuypers J, Krieger JN. Role of human papillomavirus typing in diagnosis and clinical decision making for a giant verrucous genital lesion. Urology53, 627–630 (1999).
   PubMedGoogle Scholar
• Gross G, Pfister H. Role of human papillomavirus in penile cancer, penile intraepithelial squamous cell neoplasias and in genital warts. Med. Microbiol. Immunol. (Berl.).193, 35–44 (2004).
   PubMed Web of Science ®Google Scholar
• Cubilla AL, Velazques EF, Reuter VE, Oliva E, Mihm MC Jr, Young RH. Warty (condylomatous) squamous cell carcinoma of the penis: a report of 11 cases and proposed classification of ‘verruciform’ penile tumours. Am. J. Surg. Pathol.24, 505–512 (2000).
   PubMed Web of Science ®Google Scholar
• Bezerra AL, Lopes A, Landman G, Alencar GN, Torlonii H, Villa LL. Clinicopathologic features and human papillomavirus DNA prevalence of warty and squamous cell carcinoma of the penis. Am. J. Surg. Pathol.25, 673–678 (2001).
   PubMedGoogle Scholar
• McKenna KE, Patterson CC, Handley J, McGinn S, Allen G. Cutaneous neoplasia following PUVA therapy for psoriasis. Br. J. Dermatol.134, 639–642(1996).
   PubMedGoogle Scholar
• Yoneta A, Yamashita T, Jin HY, Iwasawa A, Kondo S, Jimbow K. Development of squamous cell carcinoma by two high-risk human papillomaviruses (HPVs), a novel HPV-67 and HPV-31 from Bowenoid papulosis. Br. J. Dermatol.143, 604–608 (2000).
   PubMedGoogle Scholar
• Eisen RF, Bhawan J, Cahn TH. Spontaneous regression of Bowenoid papulosis of the penis. Cutis32, 269–272 (1983).
   PubMedGoogle Scholar
• Wolbarst AL. Circumcision and penile cancer. Lancet1, 150–153 (1932).
   Google Scholar
• Schrek R, Lenowitz H. Etiological factors in carcinoma of the penis. Cancer Res.7, 180–187 (1947).
   PubMed Web of Science ®Google Scholar
• Tsen HE, Morgenstern H, Mack T, Peters RK. Risk factors for penile cancer: results of a population-based case-control study in Los Angeles County (United States). Cancer Causes Control12, 267–277 (2001).
   PubMed Web of Science ®Google Scholar
• Melmed EP, Payne JR. Carcinoma of the penis in a Jew circumcised in infancy. Br. J. Surg.54, 729–731 (1967).
   PubMedGoogle Scholar
• Lucia MS, Miller GJ. Histopathology of malignant lesions of the penis. Urol. Clin. N. Am.19, 227–246 (1992).
   PubMed Web of Science ®Google Scholar
• Muir CS, Nectoux J. Epidemiology of carcinoma of the testis and penis. USA Natl Cancer Inst. Monographs53, 157–164 (1979).
   Google Scholar
• Reddy CRRM, Devendranath V, Pratap S. Carcinoma of the penis: role of phimosis. Urology24, 85–88 (1984).
   PubMedGoogle Scholar
• Dillner J, von Krogh G, Horenblas S, Meijer CJ. Etiology of squamous cell carcinoma of the penis. Scand. J. Urol. Nephrol.205(Suppl.), 189–193 (2000).
   Google Scholar
• Hellberg D, Valentin J, Eklund T et al. Penile cancer: is there an epidemiological role for smoking and sexual behaviour. Br. Med. J.295, 1306–1308 (1987).
   PubMed Web of Science ®Google Scholar
• Selli C, Scott CA, De Antoni P, Moro U, Crisci A, Cartei G. Squamous cell carcinoma arising at the base of the penis in a burn scar. Urology54, 923 (1999).
   PubMedGoogle Scholar
• Ciancio SJ, Coburn M. Penile salvage for squamous cell carcinoma associated with mineral oil injection. J. Urol.164, 1650 (2000).
   PubMedGoogle Scholar
• Daling JR, Madeleine MM, Johnson LG et al. Penile cancer: importance of circumcision, human papillomavirus and smoking in in situ and invasive disease. Int. J. Cancer116, 606–616 (2005).
   PubMed Web of Science ®Google Scholar
• Moore TO, Moore AY, Carrasco D et al. Human papillomavirus, smoking and cancer. J. Cutan. Med. Surg.5, 323–328 (2001).
   PubMedGoogle Scholar
• Sasson IM, Haley NJ, Hoffman D, Wynder EL et al. Cigarette smoking and neoplasia of the uterine cervix: smoke constituents incervical mucus. N. Engl. J. Med.312, 315–316 (1985).
   PubMed Web of Science ®Google Scholar
• Winkelstein W Jr. Smoking and cancer of the uterine cervix. Am. J. Epidemiol.106, 257–259 (1977).
   PubMed Web of Science ®Google Scholar
• Castonguay A, Tjdve H, Hecht SS. Tisue distribution of the the tobacco specific carcinogen4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone and its metabolites in F344 rats. Cancer Res.43, 630–638 (1983).
   PubMed Web of Science ®Google Scholar
• Previte SR, Karian S, Cho SI, Austen G. Penile carcinoma in renal transplant recipient. Urology13, 298–299 (1979).
   PubMedGoogle Scholar
• Stern RS. Genital tumours among men with psoriasis exposed to psoralens and ultraviolet A radiation (PUVA) and ultraviolet B radiation. N. Engl. J. Med.322, 1093–1097 (1990).
   PubMed Web of Science ®Google Scholar
• Perkins W, Lamont D, MacKie RM. Cutaneous malignancy in males treated with photochemotherapy. Lancet336(8725), 1248 (1990).
   PubMedGoogle Scholar
• de la Brassinne M, Richert B. Genital squamous cell carcinoma after PUVA therapy. Dermatology185, 316–318 (1992).
   PubMedGoogle Scholar
• Fryrear RS, Wiggins AK, Sangueza O, Yosipovitch G. Rapid onset of cutaneous squamous cell carcinoma of the penis in a patient with psoriasis on etanercept therapy. J. Am. Acad. Dermatol.51, 1026 (2004).
   PubMed Web of Science ®Google Scholar
• Poblet E, Alfaro L, Fernander-Segoviano P, Jimenez-Reyes J, Salido EC. Human papillomavirus-associated penile squamous cell carcinoma in HIV positive patients. Am. J. Surg. Pathol.23, 1119–1123 (1999).
   PubMedGoogle Scholar
• Gomousa-Michael M, Gialama E, Gomousas N, Gialama G. Genital human papillomavirus infection and associated penile intraepithelial neoplasia in males infected with the human immunodeficiency virus. Acta Cytol.44, 305–309 (2000).
   PubMedGoogle Scholar
• Aboulafia DM, Gibbons R. Penile cancer and human papilloma virus (HPV) in a human immunodeficiency virus (HIV)-infected patient. Cancer Invest.19, 266–272 (2001).
   PubMed Web of Science ®Google Scholar
• Theodore C, Androulakis N, Spatz A, Goujard C, Blanchet P, Wilbault P. An explosive course of squamous cell penile cancer in an AIDS patient. Ann. Oncol.13, 475–479 (2002).
   PubMedGoogle Scholar
• Demopoulos BP, Vamvakas E, Ehrlich JE, Demopoulos R. Non-acquired immunodeficiency syndrome-defining malignancies in patients infected with human immunodeficiency virus. Arch. Pathol. Lab. Med.127, 589–592 (2003).
   PubMedGoogle Scholar
• Keerti VS. Human papillomaviruses and anogenital cancers. N. Engl. J. Med.337, 1386–1387 (1997).
   PubMedGoogle Scholar
• Smith PG, Kinlen LJ, White GC et al. Mortality of wives of men dying with cancer of the penis. Br. J. Cancer41, 422–428 (1980).
   PubMed Web of Science ®Google Scholar
• Barrasso R, De Brux J, Croissant O, Orth G. High prevalence of papillomavirus associated penile intraepithelial neoplasia in partners of women with cervical intraepithelial neoplasia. N. Engl. J. Med.317, 916–923 (1987).
   PubMed Web of Science ®Google Scholar
• Kennedy L, Buntine DW, O’Connor D, Frazer IH. Human papillomavirus – a study of male sexual partners. Med. J. Aust.149, 309–311 (1988).
   PubMedGoogle Scholar
• Zabbo A, Stein BS. Penile intraepithelial neoplasia in patients examined for exposure to human papilloma virus. Urology41, 24–26 (1993).
   PubMedGoogle Scholar
• Ikenberg H, Gissmann L, Gross G, Grussendorf-Cohen EI, zur Hausen H. Human papillomavirus Type 16 DNA in genital Bowen’s disease and in Bowenoid papulosis. Int. J. Cancer32, 563–565 (1983).
   PubMed Web of Science ®Google Scholar
• Boshart M, Gissmann L, Ikenberg H, Kleinheinz A, Scheurien W, zur Hausen H. A new type of papillomavirus DNA, its presence in genital cancer biopsies and in cell lines derived from cervical cancer. EMBO J.3, 1151–1157 (1984).
   PubMed Web of Science ®Google Scholar
• Durst M, Kleinheinz A, Hotz M, Gissmann L. The physical state of human papillomavirus Type 16 DNA in benign and malignant genital tumours. J. Gen. Virol.6, 1515–1522 (1985).
   Google Scholar
• Dianzani C, Bucci M, Pierangelli A, Calvieri S, Degener AM. Association of human papillomavirus Type 11 with carcinoma of the penis. Urology51, 1046–1048 (1998).
   PubMedGoogle Scholar
• Inagaaki H, Nonaka M, Eimoto T. Bowenoid papulosis showing polyclonal nature. Diagn. Mol. Pathol.70, 122–126 (1998).
   Google Scholar
• Meyer T, Arndt R, Christophers E et al. Association of rare human papillomavirus types with genital premalignant and malignant lesions. J. Infect. Dis.178, 252–255 (1998).
   PubMedGoogle Scholar
• Loning T, Riviere A, Henke RP, von Preyss S, Dorner A. Penile/anal condylomas and squamous cell cancer. A HPV DNA hybridization study. Virchows Arch.413, 491–498 (1988).
   Google Scholar
• Griffiths TRL, Mellon JK. Human papillomavirus and urological tunours: basic science and role in penile cancer. BJU Int.84, 579–586 (1999).
   PubMedGoogle Scholar
• Wieland U, Jurk S, Weissenborn S et al. Erythroplasia of Queyrat: coinfection with cutaneous carcinogenic human papillomavirus Type 8 and genital papillomaviruses in a carcinoma in situ. J. Invest. Dermatol.115, 396–401 (2000).
   PubMed Web of Science ®Google Scholar
• Salazar EL, Mercado E, Calzada L. Human papillomavirus hpv-16 DNA as an epitheliotropic virus that induces hyperproliferation in squamous penile tissue. Arch. Androl.51, 327–334 (2005).
   PubMed Web of Science ®Google Scholar
• Buonaguro FM, Tornesello ML, Salatiello I. The Uganda study on HPV variants and genital cancers. J. Clin. Virol.19, 31–41 (2000).
   Google Scholar
• Suzuki H, Sato N, Kodama T et al. Detection of human papillomavirus DNA and state of p53 gene in Japanese penile cancer. Jpn. J. Clin. Oncol.24, 1–6 (1994).
   PubMed Web of Science ®Google Scholar
• Rubin MA, Kleter B, Zhou M et al. Detection and typing of human papillomavirus DNA in penile carcinoma: evidence for multiple independent pathways of penile carcinogenesis. Am. J. Pathol.159, 1211–1218 (2001).
   PubMed Web of Science ®Google Scholar
• Bezerra AL, Lopes A, Santiago GH, Ribeiro KC, Latorre MR, Villa LL. Human papillomavirus as a prognostic factor in carcinoma of the penis: analysis of 82 patients treated with amputation and bilateral lymphadenectomy. Cancer91, 2315–2321 (2001).
   PubMed Web of Science ®Google Scholar
• Dillner J, Meijer CJ, von Krogh G, Horenblas S. Epidemiology of human papillomavirus infection. Scand. J. Urol. Nephrol.205(Suppl.), 194–200 (2000).
   Google Scholar
• Perez VG, Eres Saez FJ, Ramada Benlloch FJ et al. Association of giant condyloma acuminatum of the penis with intraurethral simple condylomata. Apropos of a case. Arch. Espanol. Urol.44, 1103–1105 (1991).
   PubMedGoogle Scholar
• Noel JC, Vandenbossche M, Peny MO et al. Verrucous carcinoma of the penis: importance of human papillomavirus typing for diagnosis and therapeutic decision. Eur. Urol.22, 83–85 (1992).
   PubMedGoogle Scholar
• Boshart M, zur Hausen H. Human papillomaviruses in Buschke-Lowenstein tumours: physical state of the DNA and identification of a tandem duplification in the noncoding region of a human papillomavirus 6 subtype. J. Virol.58, 963–966 (1986).
   PubMedGoogle Scholar
• Grassegger A, Hopfl R, Hussl H, Wicke K, Fritsch P. Buschke-Loewenstein tumour infiltrating pelvic organs. Br. J. Dermatol.130, 221–225 (1994).
   PubMed Web of Science ®Google Scholar
• O’Gorman-Lalor O, Walker NPJ, Mathews S, Francis N, Dinneen M, Bunker CB. Successful treatment of Buschke-Lowenstein tumour of the penis with carbon dioxide laser vaporisation. Clin. Exp. Dermatol. (In Press).
   Google Scholar
• Heyns CF, van Vollenhoven P, Steenkamp JW, Allen FJ. Cancer of the penis – a review of 50 patients. S. Afr. J. Surg.35, 120–124 (1997).
   PubMedGoogle Scholar
• Lalla SC, Aldridge RD, Tidman MJ. Carcinoma of the penis presenting with dermatomyositis. Clin. Exp. Dermatol.26, 558 (2001).
   PubMedGoogle Scholar
• Velazquez EF, Barreto JE, Rodriguez I, Piris A, Cubilla AL. Limitations in the interpretation of biopsies in patients with penile squamous cell carcinoma. Int. J. Surg. Pathol.12, 139–146 (2004).
   PubMed Web of Science ®Google Scholar
• Cubilla AL, Reuter V, Velazquez E, Piris A, Saito S, Young RH. Histologic classification of penile carcinoma and its relation to outcome in 61 patients with primary resection. Int. J. Surg. Pathol.9, 111–120 (2001).
   PubMed Web of Science ®Google Scholar
• Velazquez EF, Melamed J, Barreto JE, Aguero F, Cubilla AL. Sarcomatoid carcinoma of the penis: a clinicopathological study of 15 cases. Am. J. Surg. Pathol.29, 1152–1158 (2005).
   PubMed Web of Science ®Google Scholar
• Cubilla AL, Piris A, Pfanni R, Rodriguez I, Aguero F, Young RH. Anatomic levels: important landmarks in penectomy specimens: a detailed anatomic and histologic study based on examination of 44 cases. Am. J. Surg. Pathol.25, 1091–1094 (2001).
   PubMedGoogle Scholar
• Ono Y, Ozawa M, Tamura Y et al. Tumor-associated tissue eosinophilia of penile cancer. Int.J. Urol.9, 82–87 (2002).
   Google Scholar
• Berdjis N, Meye A, Nippgen J et al. Expression of Ki-67 in squamous cell carcinoma of the penis. BJU Int.96, 146–148 (2005).
   PubMedGoogle Scholar
• Alves G, Fiedler W, Guenther E, Nascimento P, Campos MM, Ornellas AA. Determination of telomerase activity in squamous cell carcinoma of the penis. Int. J. Oncol.18, 67–70 (2001).
   PubMedGoogle Scholar
• Schwartz RA. Buschke-Loewenstein tumor. Verrucous carcinoma of the penis. J. Am. Acad. Dermatol.23, 723–772 (1993).
   Google Scholar
• Ouban A, Dellis J, Salup R, Morgan M. Immunohistochemical expression of Mdm2 and p53 in penile verrucous carcinoma. Ann. Clin. Lab. Sci.33, 101–106 (2003).
   PubMedGoogle Scholar
• Saeed S, Keehn CA, Khalil FK, Morgan MB. Immunohistochemical expression of Bax and Bcl02 in penile carcinoma. Ann. Clin. Lab. Sci.35, 91–96 (2005).
   PubMed Web of Science ®Google Scholar
• Sturm JT, Christenson CE, Vecker JH et al. Squamous cell carcinoma of the anus arising in a giant condyloma acuminatum. Dis. Colon Rectum18, 147–151 (1975).
   PubMedGoogle Scholar
• Johnson DE, Lo RK, Srigley J, Ayala AG. Vererucous carcinoma of the penis. J. Urol.133, 216–218 (1985).
   PubMed Web of Science ®Google Scholar
• Hull MT, Eble JN, Priest JB, Mulcahy JJ. Ultrastructure of Buschke-Loewenstein tumor. J. Urol.126, 485–489 (1981).
   PubMedGoogle Scholar
• Ikeda R, Kobayashi Y, Shiroma K, Suzuki K, Ueda Y. Telomerase activity in giant condyloma acuminatum. Urol. Int.65, 220–223 (2000).
   PubMedGoogle Scholar
• von Krogh G, Horenblas S. The Management and prevention of premalignant penile lesions. Scand. J. Urol. Nephrol.205(Suppl.), 220–229 (2000).
   Google Scholar
• Fulton JE, Carter DM, Hurley HJ. Treatment of Bowen’s disease with topical 5-fluorouracil under occlusion. Arch. Dermatol.97, 178 (1968).
   PubMedGoogle Scholar
• Lynch JL. Erythroplasia of Queyrat. Arch. Dermatol.100, 782 (1969).
   Google Scholar
• Huesner JN, Pugh RP. Erythroplasia of Queyrat treated with topical 5-fluorouracil. J. Urol.102, 595–597 (1969).
   PubMedGoogle Scholar
• Lewis RJ, Bendl BJ. Erythroplasia of Queyrat-report of a patient successfully treated with topical 5-fluorouracil. Can. Med. Assoc. J.104, 148–149 (1971).
   PubMedGoogle Scholar
• Goette DK, Elgart M, deVillez RL Erythroplasia of Queyrat. Treatment with topically applied fluorouracil. JAMA232, 934–937 (1975).
   PubMed Web of Science ®Google Scholar
• Tolia BM, Castro VL, Mouded IM et al. Bowen’s disease of the shaft of the penis. Successful treatment with 5-fluorouracil. Urology7, 617–619 (1976).
   PubMedGoogle Scholar
• Goette DK, Carson TE. Erythroplasia of Queyrat. Treatment with topical 5-fluorouracil. Cancer38, 1498–1502 (1976).
   PubMed Web of Science ®Google Scholar
• Sturm HM. Bowen’s disease and 5-fluorouracil. J. Am. Acad. Dermatol.1, 513–522 (1979).
   PubMedGoogle Scholar
• Kossow AS, Cotelingham JD, Macfarland F. Bowenoid papulosis of the penis. J. Urol.125, 124–126 (1980).
   Google Scholar
• Arlette JP. Treatment of Bowen’s disease and erythroplasia of Queyrat. Br. J. Dermatol.149, 43–49 (2003).
   PubMed Web of Science ®Google Scholar
• Sonnex TS, Ralfs IG, Plaza de Lanza M, Dawber RP. Treatment of erythroplasia of Queyrat with liquid nitrogen cryosurgery. Br. J. Dermatol.106, 581–584 (1982).
   PubMed Web of Science ®Google Scholar
• Brown MD, Zachary CB, Grekin RC, Swanson NA. Penile tumours: their management by Moh’s micrographic surgery. J. Dermatol. Surg. Oncol.13, 1163–1167 (1987).
   PubMedGoogle Scholar
• Brown MD, Zachary CB, Grekin RC, Swanson NA. Genital tumours: their management by micrographic surgery. J. Am. Acad. Dermatol.18, 115–122 (1988).
   PubMedGoogle Scholar
• Boyton KK, Bjorkman DJ. Argon laser therapy for perianal Bowen’s disease: a case report. Lasers Surg. Med.11, 385–387 (1991).
   PubMedGoogle Scholar
• Knoll LD, Segura JW, Benmson RC Jr, Goellner JR. Bowenoid papulosis of the penis: successful management with neodymium: YAG laser. J. Urol.139, 1307–1309 (1988).
   PubMed Web of Science ®Google Scholar
• Greenbaum SS, Glogau R, Stegman SJ, Tromovitch TA. Carbon dioxide laser treatment of erythroplasia of Queyrat. J. Dermatol. Surg. Oncol.15, 747–750 (1989).
   PubMedGoogle Scholar
• Petrelli NJ, Cebollero JA, Rodriguez-Bigas M, Mang T. Photodynamic therapy in the management of neoplasms of the perianal skin. Arch. Dermatol.127, 1436–1438 (1992).
   Google Scholar
• Stables GI, Stringer MR, Robinson DJ, Ash DV. Erythroplasia of Queryat treated by topical aminolaevulinic acid photodynamic therapy. Br. J. Dermatol.140, 514–517 (1999).
   PubMed Web of Science ®Google Scholar
• Harth Y, Hirshovitz B. Topical photodynamic therapy in basal and squamous cell carcinoma and penile Bowen’s disease with 20% aminolevulinic acid, and exposure to red light and infrared light. Harefuah134, 602–605 (1998).
   PubMedGoogle Scholar
• Lee MR, Ryman W. Erythroplasia of Queyrat treated with topical methyl aminolevulinate photodynamic therapy. Australas J. Dermatol.46, 196–198 (2005).
   PubMedGoogle Scholar
• Yang CH, Lee JC, Chen CH, Hui CY, Hong HS, Kuo HW. Photodynamic therapy for Bowenoid papulosis using a novel incoherent light-emitting diode device. Br. J. Dermatol.149, 1297–1299 (2003).
   PubMedGoogle Scholar
• Snoeck R, Van Laethem Y, De Clercq E, De Mauneuge J, Clumeck N. Treatment of a Bowenoid papulosis of the penis with local applications of cidofovir in a patient with acquired immunodeficiency syndrome. Arch. Int. Med.161, 2382–2384 (2001).
   PubMedGoogle Scholar
• Calista D. Topical cidofovir for erythroplasia of Queyrat of the glans penis. Br. J. Dermatol.147, 399–400 (2002).
   PubMed Web of Science ®Google Scholar
• Kaspari M, Gutzmer R, Kiehl P, Dumke P, Kapp A, Brodersen JP. Imiquimod 5% cream in the treatment of human papillomavirus-16-positive erythroplasia of Queyrat. Dermatology205, 67–69 (2002).
   PubMedGoogle Scholar
• Goorney BP, Polori R. A case of Bowenoid papulosis of the penis successfully treated with topical imiquimod cream 5%. Int. J. STD AIDS15, 833–835 (2004).
   PubMedGoogle Scholar
• Danielsen AG, Sand C, Weismann K. Treatment of Bowen’s disease of the penis with imiquimod 5% cream. Clin. Exp. Dermatol.28, 7–9 (2003).
   PubMed Web of Science ®Google Scholar
• Micali G, Nasca MR, Tedeschi A. Topical treatment of intraepithelial penile carcinoma with imiquimod. Clin. Exp. Dermatol.28, 4–6 (2003).
   PubMed Web of Science ®Google Scholar
• Orengo I, Rosen T, Guill CK. Treatment of squamous cell carcinoma in situ of the penis with 5% imiquimod cream: a case report. J. Am. Acad. Dermatol.47, S225–S2258 (2002).
   Web of Science ®Google Scholar
• Schroeder TL, Sengelmann RD. Squamous cell carcinoma in situ of the penis successfully treated with imiquimod 5% cream. J. Am. Acad. Dermatol.46, 545–548 (2002).
   PubMed Web of Science ®Google Scholar
• Wysocki WM, Komorowski AL, Kolodziejski LS, Wysocka J. Synchronous anal and penile cancers. Int J. Urol.11, 1139–11341 (2004).
   PubMedGoogle Scholar
• Mosconi AM, Roila F, Gatta G, Theodore C. Cancer of the penis. Crit. Rev. Oncol. Hematol.53, 165–177 (2005).
   PubMedGoogle Scholar
• Kroon BK, Horenblas S, Nieweg OE. Contemporary management of penile squamous cell carcinoma. J. Surg. Oncol.89, 43–50 (2005).
   PubMedGoogle Scholar
• Solsona E, Algaba F, Horenblas S, Pizzocaro G, Windahl T. European Association of Urology EUA Guidelines on Penile Cancer. Eur. Urol.46, 1–8 (2004).
   PubMed Web of Science ®Google Scholar
• Singh I, Khaitan A. Current trends in the management of carcinoma penis – a review. Int. Urol. Nephrol.35, 215–225 (2003).
   PubMedGoogle Scholar
• Micali G, Nasca MR, Innocenzi D, Schwartz RA. Invasive penile carcinoma: a review. Dermatol. Surg.30, 311–320 (2004).
   PubMedGoogle Scholar
• Stancik I, Holtl W. Penile cancer: review of the recent literature. Curr. Opin. Urol.13, 467–472 (2003).
   PubMedGoogle Scholar
• Harden SV, Tan LT. Treatment of localized carcinoma of the penis: a survey of current practice in the UK. Clin. Oncol. (R. Coll. Radiol.)13, 284–287 (2001).
   PubMedGoogle Scholar
• Munro NP, Thomas PJ, Deutsch GP, Hodson NJ. Penile cancer: a case for guidelines. Ann. R. Coll. Surg. Engl.83, 180–185 (2001).
   PubMedGoogle Scholar
• Siow WY, Cheng C. Penile cancer: current challenges. Can. J. Urol.12, 18–23 (2005).
   PubMedGoogle Scholar
• Schoeneich G, Perabo FG, Muller SC. Squamous cell carcinoma of the penis. Andrologia31(Suppl. 1), 17–20 (1999).
   PubMedGoogle Scholar
• Pietrzak P, Corbishley C, Watkin N. Organ-sparing surgery for invasive penile cancer: early follow-up data. BJU Int.95, 1253–1257 (2004).
   Google Scholar
• Agrawal A, Pai D, Ananthakrishnan N, Smile SR, Ratnakar C. Clinical and sonographic findings in carcinoma of the penis. J. Clin. Ultrasound28, 399–406 (2000).
   PubMedGoogle Scholar
• Lont AP, Besnard AP, Gallee MP, van Tinteren H, Horenblas S. A comparison of physical examination and imaging in determining the extent of primary penile carcinoma. BJU Int.91, 493–495 (2003).
   PubMedGoogle Scholar
• Scardino E, Villa G, Bonomo G et al. Magnetic resonance imaging combined with artificial erection for local staging of penile cancer. Urology63, 1158–1162 (2004).
   PubMedGoogle Scholar
• Agrawal A, Pai D, Ananthakrishnan N, Smile SR, Ratnakar C. The histological extent of the local spread of carcinoma of the penis and its therapeutic implications. BJU Int.85, 299–301 (2000).
   PubMed Web of Science ®Google Scholar
• McDougal WS, Kirchner FR, Edwards RH, Killion LZ. Treatment of carcinoma of the penis: the case for primary lymphadenectomy. J. Urol.136, 38–41 (1986).
   PubMed Web of Science ®Google Scholar
• Dexeus FH, Logothetis J, Sella A et al. Combination therapy with methotrexate, bleomycin and cisplatin for advanced squamous cell carcinoma of the male genital tract. J. Urol.146, 1284–1287 (1991).
   PubMedGoogle Scholar
• James N. Chemoradiotherapy for penile cancer. In: The Effective Management of Urological Malignancies. Anderson J, Oliver RTD, Miles A (Eds). Aesculapius Medical Press, London, UK (2005).
   Google Scholar
• Laniado ME, Lowdell C, Mitchell H, Christmas TJ. Squamous cell carcinoma antigen: a role in the early identification of nodal metastases in men with squamous cell carcinoma fo the penis. BJU Int.92, 248–250 (2003).
   PubMed Web of Science ®Google Scholar
• Kommu S, Hadway P, Watkin N. Squamous cell carcinoma antigen as a biomarker for penile cancer. BJU Int.95, 478–479 (2005).
   PubMedGoogle Scholar
• Rippentrop JM, Joslyn SA, Konety BR. Squamous cell carcinoma of the penis: evaluation of data from the surveillance, epidemiology and end results program. Cancer101, 1357–1363 (2004).
   PubMed Web of Science ®Google Scholar
• Sanchez-Ortiz RF, Pettaway CA. Natural history, management, and surveillance of recurrent squamous cell penile carcinoma: a risk-based approach. Urol. Clin. N. Am.30, 853–867 (2003).
   PubMed Web of Science ®Google Scholar
• South LM, O’Sullivan JP, Gazet JC. Giant condylomata of Buschke and Lowenstein. Clin. Oncol.3, 107–115 (1977).
   PubMed Web of Science ®Google Scholar
• Tessler AN, Applebaum SM. The Buschke-Lowenstein tumor. Urology20, 36–39 (1982).
   PubMedGoogle Scholar
• Creasman C, Haas PA, Fox TA Jr., Balazas M. Malignant transformation of anorectal giant condyloma acuminatum (Buschke-Loewenstein tumour). Dis. Colon Rectum32, 481–487 (1989).
   PubMedGoogle Scholar
• Lenk S, Oesterwitz H, Audring H. Laser surgery in superficial penile tumours. Int. Urol. Nephrol.23, 357–363 (1991).
   PubMedGoogle Scholar
• Risse L, Negrier P, Dang PM et al. Treatment of verrucous carcinoma with recombinant α-interferon. Dermatology190, 142–144 (1995).
   PubMedGoogle Scholar