Cutaneous sarcoidosis. Issue 877 (November 1998)

• Record Type: Journal Article
• Authors: Wilson, N. J.; King, C. M.
• Is Part Of: Postgraduate medical journal. Volume 74:Issue 877(1998)
• Page Start: 649
• Page End: 652
• Publication Date: 1998-11
• Subjects: Medicine -- Periodicals; 610
• DOI: 10.1136/pgmj.74.877.649
• Languages: English
• ISSNs: 0032-5473

Abstract

Abstract : Sarcoidosis is a multi-organ granulomatous disorder of unknown cause. Skin sarcoidosis occurs in about 25% of patients with systemic disease and may also arise in isolation. A wide range of clinical presentations of cutaneous sarcoidosis is recognised. The diagnosis rests on the presence of non-caseating granulomas on skin biopsy and the exclusion of other granulomatous skin disease. The treatment and overall prognosis of cutaneous sarcoidosis is primarily dependent on the degree of systemic involvement. In patients with aggressive disease limited to the skin immunosuppressive therapy may be indicated.