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 presentatio
ns 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 prognos
is of cutaneous sarcoidosis is primarily dependent on the degree of sy
stemic involvement. In patients with aggressive disease limited to the
skin immunosuppressive therapy may be indicated.