Background: CD30+ cutaneous lymphoproliferative disorders (CLPDs) include lymphomatoid papulosis, borderline cases of CD30+CLPDs, and primary cutaneous anaplastic large cell lymphoma (PCALCL). Prior studies have shown CD30+CLPDs have an excellent prognosis.
Objective: We sought to present the single-center experience of Stanford University, Stanford, Calif, in the management of CD30+CLPDs.
Objectives: To study and update the clinical characteristics and long-term outcome of our patients with mycosis fungoides (MF) and Sézary syndrome (SS), and to identify important clinical factors predictive of survival and disease progression.
Design: A single-center, retrospective cohort analysis.
Setting: Academic referral center for cutaneous lymphoma.