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CLINICAL

Facial growth in a patient with psoriasis

Rita S Matos, Tiago Torres

Case generalised or localised. Each of these interrupts the signalling pathway for A , 47 years of age, with types is further divided into congenital interleukin-2 production and inhibits the chronic plaque-type psoriasis for the and acquired subtypes.1 It can be a proliferation of cluster of differentiation past 18 years but otherwise healthy, manifestation of a more general medical 4 (CD4) T-lymphocytes.7 One possible presented complaining of problem. The possible causes of mechanism for may be growth three months after starting acquired hypertrichosis are summarised the expression of several growth factors systemic cyclosporine therapy (3.5 in Table 1.1 and production of other cytokines.2,4 mg/kg/day). The patient had been Hypertrichosis must not be confused Hypertrichosis is one of the most previously treated with topical agents with , which is defined as common side effects of systemic and narrowband ultraviolet B (NB-UVB) -induced growth of terminal cyclosporine therapy, although there phototherapy. On physical examination, hair in women and children, in a is considerable variability in the she had marked facial hair growth male pattern distribution. Hirsutism reported incidence.8 It is a dose- and improvement of psoriasis severity is androgen-dependent, whereas dependent phenomenon and usually (Figure 1). No other skin lesions or hypertrichosis is not.1 noted a few months after cyclosporine symptoms were detected. therapy begins.1 Other possible Answer 2 indications for cyclosporine include Question 1 The most likely aetiology for rheumatic diseases (eg rheumatoid What is the pathogenesis of this hypertrichosis in this patient is arthritis), ulcerative colitis and various phenomenon? cyclosporine therapy. Cyclosporine is an other immune-mediated diseases. effective drug used for the treatment of Cyclosporine is also the backbone Question 2 psoriasis.4–6 It is an immunomodulating of immunosuppression in transplant What is the most likely aetiology for agent that binds to cyclophilin, a recipients, particularly those with renal hypertrichosis in this patient? cytoplasmic protein. Cyclosporine transplants.3 Question 3 Are there other possible side effects? Question 4 How would you manage this patient? Answer 1 Hypertrichosis is excessive hair growth on any part or whole of the body, compared with people of the same age, A B sex and racial group.1 The underlying pathogenesis remains unknown.2,3 Figure 1. Clinical appearance of patient’s facial hair Hypertrichosis is usually classified as

© The Royal Australian College of General Practitioners 2016 AFP VOL.45, NO.9, SEPTEMBER 2016 641 CLINICAL FACIAL HAIR GROWTH

Answer 3 or biological agents (anti-TNFα, anti-p40 e Authors There are other cutaneous side effects anti-IL17).10 Rita S Matos MD, General Practice trainee, Unidade de Saúde Familiar São Bento – Agrupamento of cyclosporine, such as epidermal , When it is not possible to stop de Centros de Saúde de Gondomar, Portugal. keratosis pilaris, , and cyclosporine, hypertrichosis can [email protected] .8 The other side be managed by physical methods Tiago Torres MD, PhD, Dermatologist, Department of Dermatology and Dermatology Research Unit, effects are summarised in Table 2. (eg , , ), Centro Hospitalar do Porto; Instituto de Ciências chemical depilation, laser sources or Biomédicas Abel Salazar, University of Porto, Answer 4 pharmacological treatment with topical Portugal 1 Competing interests: Outside this work, Tiago Cessation of cyclosporine therapy . Torres has received payment from Pfizer, Abbvie, results in a progressive resolution of the Novartis, Janssen, MSD, Leo-Pharma and Lilly for induced hypertrichosis.3,9 The decision to Key points board memberships, consultancy, expert testimony and speaking engagements. He has also received discontinue systemic treatment should • Hypertrichosis is one of the most grants from MSD and Leo-Pharma; and Pfizer, include a risk–benefit assessment for that common side effects of systemic Abbvie, Novartis, Janssen, MSD and Leo-Pharma have covered expenses. particular patient. The patient’s psoriasis cyclosporine therapy. It is dose- Provenance and peer review: Not commissioned, will probably be aggravated following dependent and usually noted a few externally peer reviewed. cyclosporine cessation. Other possible months after beginning therapy. References systemic treatments can be considered • Cessation of cyclosporine results in a 1. Valia, RG. Hypertrichosis. Indian J Dermatol on a case-by-case basis. These systemic progressive resolution of the induced 2005;50(3):119–24. treatments include methotrexate, acitretin hypertrichosis. 2. Xu W, Fan W, Yao K. Cyclosporine – A stimulated hair growth from mouse vibrissae follicles in an organ culture model. J Biomed Res 2012;26(5):372–80. 3. Panicker VV, Mathew A, Dhamramaratnam AD. Table 1. Possible causes for acquired hypertrichosis Cosmetically disfiguring side effects of cyclosporine. Int J Trichology 2012;4(1):50. Congenital generalised Congenital hypertrichosis lanuginose 4. Rosmarin DM, Lebwohl M, Elewski BE, Universal congenital hypertrichosis Gottlieb AB. Cyclosporine and psoriasis: 2008 National Psoriasis Foundation Acquired generalised Hypertrichosis lanuginosa associated with malignancy Consensus Conference. J Am Acad Dermatol Endocrine disorders (eg thyroid disorders and disorders of 2010;62(5):838–53. diencephalon or pituitary) 5. Clarke P. Psoriasis. Aust Fam Physician 2011;40(7):468–73. Malnutrition (eg celiac disease, ) 6. Amor KT, Ryan C, Menter A. The use of Drugs (eg , acetazolamide, cyclosporine, penicillamine) cyclosporine in dermatology: Part I. J Am Acad Dermatol 2010;63(6):925–46. Congenital localised Melanocytic naevi 7. Lei HL, Ku WC, Sun MH, Chen KJ, Lai JY, Lumbosacral hypertrichosis Sun CC. Cyclosporine – A eye drop-induced elongated : A case report. Case Rep Acquired localised Becker’s naevus Ophthalmol 2011;2(3):398–400. cutanea tarda 8. Ryan C, Amor KT, Menter A. The use of Trauma cyclosporine in dermatology: Part II. J Am Acad Dermatol 2010;63(6):949–72. Infection 9. Wysocki GP, Daley TD. Hypertrichosis in patient (areas overlying thrombophlebitis or chronic receiving cyclosporine therapy. Clin Exp osteomyelitis or vaccination sites) Dermatol 1987;12(3):191–96. 10. Cline A, Hill D, Lewallen R, Feldman SR. Current status and future prospects for biologic treatments of psoriasis. Expert Rev Clin Immunol 2016;6:1–15. Table 2. Side effects of systemic cyclosporine therapy

Cutaneous Hypertrichosis, epidermal cysts, keratosis pilaris, acne, folliculitis, sebaceous hyperplasia

Cardiovascular , hyperlipidemia (particularly hypertriglyceridemia)

Renal Nephrotoxicity

Neurologic Paresthesia, hyperesthesia, headaches, seizures, psychosis, tremor

Gastrointestinal Nausea, vomiting, diarrhea, anorexia, abdominal discomfort, hyperbilirrubinemia

Other Gingival hyperplasia, hyperuricemia, hypomagnesemia

642 AFP VOL.45, NO.9, SEPTEMBER 2016 © The Royal Australian College of General Practitioners 2016