We describe a patient presenting with B cell chronic lymphocytic leukemia (
B-CLL) who subsequently developed cutaneous infiltrates. Specimens of the b
lood, bone marrow and cutaneous infiltrations all showed the same heavy-cha
in gene rearrangement. Following failure of conventional chemotherapy, and
in view of the similarity of the disease to cutaneous T cell lymphoma, inte
rferon-cr therapy was employed with satisfactory results. Introduction of t
h is cytokine to the therapeutic modalities for secondary cutaneous B-CLL w
ould hopefully change the poor outcome of this entity, or at least could pr
oduce a better quality of life. Loss of histidine decarboxylase activity in
the infiltrating cells - in contrast to circulating lymphocytes - may be a
ssociated with the transformation of B-CLL to a more aggressive infiltrativ
e form, offering a possible explanation for tissue invasiveness. The changi
ng character of the disease raises the possibility of a second mutational e
vent in the course of B-CLL. Copyright (C) 2000 S. Karger AG. Basel.