By Nikhil Yawalkar
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44 Kimball AB, Gladman D, Gelfand JM, Gordon K, Horn EJ, Korman NJ, et al: National Psoriasis Foundation clinical consensus on psoriasis comorbidities and recommendations for screening. J Am Acad Dermatol 2008;58:1031–1042. 45 Salvarani C, Lo SG, Macchioni P, Cremonesi T, Rossi F, Mantovani W, et al: Prevalence of psoriatic arthritis in Italian psoriatic patients. J Rheumatol 1995;22:1499–1503. 35 46 Scarpa R, Oriente P, Pucino A, Torella M, Vignone L, Riccio A, et al: Psoriatic arthritis in psoriatic patients.
They are available in various strengths and formulations that enable the clinician to tailor the treatment according to the patient’s requirements and preferences. The Stoughton Cornell classification ranks the potency and clinical efficacy of topical corticosteroids on the basis of their ability to induce vasoconstriction [17]. In the UK, topical corticosteroids are classified into 4 groups; while in the USA, 7 classes are recognized. 05%), available for over 3 decades, remains the most widely used potent topical corticosteroid to treat psoriasis.
Numerous studies have tried to clarify the association of lymphoma and psoriasis. In a large population-based cohort study, 153,197 patients with psoriasis were compared to 765,950 corresponding subjects without psoriasis. In this study, an association between Hodgkin’s disease and cutaneous T cell lymphoma was shown. The authors concluded that psoriasis patients are at a higher risk of developing lymphoproliferative diseases, but, as lymphoma is a rare disease and the magnitude of association is modest, the absolute risk attributable to psoriasis is low [17].