Case Report Eruptive Condyloma Accuminata after Initiation of Infliximab Treatment for Folliculitis...

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Hindawi Publishing Corporation Case Reports in Dermatological Medicine Volume 2013, Article ID 762035, 2 pages http://dx.doi.org/10.1155/2013/762035 Case Report Eruptive Condyloma Accuminata after Initiation of Infliximab Treatment for Folliculitis Decalvans Douglas C. Wu 1 and Thomas G. Salopek 1,2 1 Division of Dermatology, Department of Medicine, University of Alberta, Edmonton, AB, Canada T6G 2G3 2 Division of Dermatology and Cutaneous Sciences, Department of Medicine, University of Alberta, 2-125 Clinical Sciences Building, Edmonton, AB, Canada T6G 2G3 Correspondence should be addressed to omas G. Salopek; [email protected] Received 2 September 2013; Accepted 4 November 2013 Academic Editors: I. D. Bassukas and K. Jimbow Copyright © 2013 D. C. Wu and T. G. Salopek. is is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. We report a patient with recalcitrant folliculitis decalvans who was placed on infliximab due to failure to respond to numerous immunosuppressive drugs and antibiotics. Aſter the second infusion of infliximab the patient reported a cutaneous eruption to the bilateral groin, penis, scrotum, perineum, and perianal region consistent with genital warts. e case highlights the need to inquire about a past or current history of genital or anal warts prior to the initiation of anti-TNF therapy, particularly with infliximab. If present, consideration should be given to concurrent antiwart therapy. 1. Introduction Folliculitis decalvans (FD) is classified as a neutrophilic primary cicatricial alopecia [1]. Clinically, FD usually affects the scalp and is characterized by erythematous follicular pustules and tuſted folliculitis with multiple hairs emerging from a single dilated follicular ostia. Colonies of Staphylo- coccus aureus are oſten present [2]. FD is oſten recalcitrant to multimodal antimicrobial and anti-inflammatory therapy. Recently, Mihaljevic and Driesch reported the successful use of infliximab for the treatment of therapy-resistant FD [3]. Included in the potential risks of anti-TNF therapy is the increased susceptibility to de novo or reactivated infections. In this report, we detail the occurrence of eruptive condyloma accuminata aſter initiation of infliximab treat- ment for therapy-resistant folliculitis decalvans. is finding highlights the need to review with patients before initiating anti-TNF therapy the possibility of having warts of any kind and in particular genital warts. 2. Case Report e case concerns a 47-year-old man with a ten-year history of recalcitrant FD. He initially presented with erythematous follicular pustules and scarring alopecia to the scalp. Inciden- tally, he was also noted to have findings consistent with a mild hidradenitis suppurativa (HS) to the groin. A biopsy of the scalp revealed very dense collections of inflammatory cells noted in the superficial reticular dermis and papillary dermis with numerous bacterial colonies within dilated follicular ostia. He underwent extensive treatment including courses of oral minocycline, clindamycin, rifampin, and dapsone; topi- cal clindamycin and antiseptic shampoos; clobetasol 0.05% lotion and intralesional triamcinolone injections; acitretin and isotretinoin; prednisone, methotrexate, and myco- phenolate mofetil. Unfortunately, these treatments and com- binations thereof failed to produce a consistent remission and the patient remained on 15–20 mg daily of prednisone to achieve mediocre control of his condition. In December 2012, infliximab infusions were initiated. Prior to commencement of infliximab therapy, it was ascer- tained that the patient was negative for HIV, hepatitis B, and hepatitis C. Additionally, a tuberculin skin test was measured at 0 mm and a screening chest X-ray revealed no evidence of tuberculosis. e patient received two infusions of infliximab at a dose of 5 mg/kg spaced 2 weeks apart. Shortly aſter his second infusion, the patient developed severe eruptive condyloma accuminata affecting his bilateral groin, penis,

Transcript of Case Report Eruptive Condyloma Accuminata after Initiation of Infliximab Treatment for Folliculitis...

  • Hindawi Publishing CorporationCase Reports in Dermatological MedicineVolume 2013, Article ID 762035, 2 pageshttp://dx.doi.org/10.1155/2013/762035

    Case ReportEruptive Condyloma Accuminata after Initiation of InfliximabTreatment for Folliculitis Decalvans

    Douglas C. Wu1 and Thomas G. Salopek1,2

    1 Division of Dermatology, Department of Medicine, University of Alberta, Edmonton, AB, Canada T6G 2G32Division of Dermatology and Cutaneous Sciences, Department of Medicine, University of Alberta, 2-125 Clinical Sciences Building,Edmonton, AB, Canada T6G 2G3

    Correspondence should be addressed toThomas G. Salopek; [email protected]

    Received 2 September 2013; Accepted 4 November 2013

    Academic Editors: I. D. Bassukas and K. Jimbow

    Copyright © 2013 D. C. Wu and T. G. Salopek. This is an open access article distributed under the Creative Commons AttributionLicense, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properlycited.

    We report a patient with recalcitrant folliculitis decalvans who was placed on infliximab due to failure to respond to numerousimmunosuppressive drugs and antibiotics. After the second infusion of infliximab the patient reported a cutaneous eruption to thebilateral groin, penis, scrotum, perineum, and perianal region consistent with genital warts.The case highlights the need to inquireabout a past or current history of genital or anal warts prior to the initiation of anti-TNF therapy, particularly with infliximab. Ifpresent, consideration should be given to concurrent antiwart therapy.

    1. Introduction

    Folliculitis decalvans (FD) is classified as a neutrophilicprimary cicatricial alopecia [1]. Clinically, FD usually affectsthe scalp and is characterized by erythematous follicularpustules and tufted folliculitis with multiple hairs emergingfrom a single dilated follicular ostia. Colonies of Staphylo-coccus aureus are often present [2]. FD is often recalcitrantto multimodal antimicrobial and anti-inflammatory therapy.Recently, Mihaljevic and Driesch reported the successfuluse of infliximab for the treatment of therapy-resistant FD[3]. Included in the potential risks of anti-TNF therapyis the increased susceptibility to de novo or reactivatedinfections. In this report, we detail the occurrence of eruptivecondyloma accuminata after initiation of infliximab treat-ment for therapy-resistant folliculitis decalvans. This findinghighlights the need to review with patients before initiatinganti-TNF therapy the possibility of having warts of any kindand in particular genital warts.

    2. Case Report

    The case concerns a 47-year-old man with a ten-year historyof recalcitrant FD. He initially presented with erythematous

    follicular pustules and scarring alopecia to the scalp. Inciden-tally, he was also noted to have findings consistent with amildhidradenitis suppurativa (HS) to the groin. A biopsy of thescalp revealed very dense collections of inflammatory cellsnoted in the superficial reticular dermis and papillary dermiswith numerous bacterial colonies within dilated follicularostia. He underwent extensive treatment including courses oforal minocycline, clindamycin, rifampin, and dapsone; topi-cal clindamycin and antiseptic shampoos; clobetasol 0.05%lotion and intralesional triamcinolone injections; acitretinand isotretinoin; prednisone, methotrexate, and myco-phenolate mofetil. Unfortunately, these treatments and com-binations thereof failed to produce a consistent remissionand the patient remained on 15–20mg daily of prednisone toachieve mediocre control of his condition.

    In December 2012, infliximab infusions were initiated.Prior to commencement of infliximab therapy, it was ascer-tained that the patient was negative for HIV, hepatitis B, andhepatitis C. Additionally, a tuberculin skin test was measuredat 0mm and a screening chest X-ray revealed no evidence oftuberculosis.The patient received two infusions of infliximabat a dose of 5mg/kg spaced 2 weeks apart. Shortly afterhis second infusion, the patient developed severe eruptivecondyloma accuminata affecting his bilateral groin, penis,

  • 2 Case Reports in Dermatological Medicine

    Figure 1: Multiple condyloma accuminata along the left inguinalfold.

    scrotum, perineum, and perianal region (Figure 1). Inflix-imab infusions were discontinued. His warts are presentlybeing treated with a combination of cryotherapy, imiquimod5% cream, and podofilox 0.5% solution. With application ofthis combination, the condyloma resolved rapidly.

    3. Discussion

    Reports of human papilloma virus (HPV) infection asso-ciated with anti-TNF therapy have thus far been rare [4–6]. Almost all cases have been associated with infliximab,although one patient developed perianal condylomata inassociation with etanercept. Other viral infections frequentlyseen by dermatologists that may be exacerbated by anti-TNF therapy include herpes zoster, primary varicella, andmolluscum contagiosum [7, 8]. Our patient did not have aknown previous history of genital condylomata and repeatedclinical examinations of his groin region (for mild HS) didnot identify any evidence of disease prior to infliximabinfusions. It is possible that hewas an asymptomatic carrier ofHPV, which became clinically apparent only in the relativelyimmunosuppressed state of TNF inhibition. Of note, hewas also on concurrent prednisone during his infliximabinfusions and this may also have exacerbated the subsequentfloridHPVeruption.Due to the risk of potential exacerbationof genital warts, patients should be informed and perhapsscreened prior to initiation of anti-TNF therapy. If thereis a history of verruca, consideration should be given toconcurrent antiwart therapy.

    Conflict of Interests

    The authors declare no conflict of interests.

    References

    [1] E. A. Olsen, W. F. Bergfeld, G. Cotsarelis et al., “Summary ofNorth American Hair Research Society (NAHRS): sponsoredworkshop on cicatricial alopecia, Duke University MedicalCenter, February 10 and 11, 2001,” Journal of the AmericanAcademy of Dermatology, vol. 48, no. 1, pp. 103–110, 2003.

    [2] C.M. Stefanato, “Histopathology of alopecia: a clinicopatholog-ical approach to diagnosis,”Histopathology, vol. 56, no. 1, pp. 24–38, 2010.

    [3] N. Mihaljevic and P. von den Driesch, “Successful use ofinfliximab in a patient with recalcitrant folliculitis decalvans,”Journal Der Deutschen Dermatologischen Gesellschaft, vol. 10,no. 8, pp. 589–590, 2012.

    [4] A. Somasekar and R. Alcolado, “Genital condylomata in apatient receiving infliximab for Crohn’s disease,” PostgraduateMedical Journal, vol. 80, no. 944, pp. 358–359, 2004.

    [5] C. Antoniou, M. G. Kosmadaki, A. J. Stratigos, and A. D.Katsambas, “Genital HPV lesions and molluscum contagiosumoccurring in patients receiving anti-TNF-𝛼 therapy,” Dermatol-ogy, vol. 216, no. 4, pp. 364–365, 2008.

    [6] S. Georgala, A. C. Katoulis, A. Kanelleas, A. Befon, and C.Georgala, “Letter: Human papilloma virus and molluscumcontagiosum lesions related to infliximab therapy for psoriasis:a case series,” Dermatology Online Journal, vol. 18, no. 4, article9, 2012.

    [7] M. J. Shale, C.H. Seow,C. S. Coffin,G.G.Kaplan, R. Panaccione,and S. Ghosh, “Review article: chronic viral infection in theanti-tumour necrosis factor therapy era in inflammatory boweldisease,”Alimentary Pharmacology andTherapeutics, vol. 31, no.1, pp. 20–34, 2010.

    [8] C. Cursiefen, M. Grunke, C. Dechant, C. Antoni, A. Jünemann,and L. M. Holbach, “Multiple bilateral eyelid molluscum conta-giosum lesions associated with TNF𝛼-antibody andmethotrex-ate therapy,” The American Journal of Ophthalmology, vol. 134,no. 2, pp. 270–271, 2002.

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