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Lymphomatoid papulosis (LyP) is a cutaneous CD30(+) lymphoproliferative disorder (LPD) characterized by chronic recurrent, self-healing papulonodular eruptions and the histological features of malignant lymphoma (1). Patients with LyP are at increased risk of developing lymphoma, particularly mycosis fungoides (MF) and anaplastic large cell lymphoma (ALCL) (1). We describe here an unusual case, in which LyP occurred in a patient with diffuse large B-cell lymphoma (DLBCL) and primary cutaneous ALCL (pcALCL). No cases of LyP associated with both pcALCL and DLBCL have been reported previously (according to a PubMed search using the terms "lymphomatoid papulosis", "diffuse large B-cell lymphoma", and "cutaneous anaplastic large cell lymphoma").

acta dermato-venereologica

Lymphomatoid Papulosis (LyP) Associated with Diffuse Large B-cell Lymphoma and Cutaneous Anaplastic Large Cell Lymphoma: LyP as a Haematological Malignancy-related Dermadrome