Lymphomatoid papulosis is a rare cutaneous lymphoproliferative disorde
r with nodular, papulonecrotic or plaque-like lesions. Although it is
clinically benign, the histology shows large, atypical lymphoid cells
that display antigenic markers of activated T-helper lymphocytes and e
xpress CD30. There is a close relationship to Hodgkin's disease and to
Ki-1-positive anaplastic large-cell lymphoma of the skin. For therapy
, various modalities such as PUVA, steroids and acyclovir have been us
ed. We report on a patient with a 10-year history of disease. Treatmen
t with interferon alfa-2a, 3 MU 3 times/week for 4 weeks, and etretina
te, 50 mg/day for 5 months, was initially successful, but lesions furt
her relapsed 5 months after cessation of the therapy.