We report the onset of an unusual blistering eruption following a diagnosis
of B-cell chronic lymphocytic leukaemia (CLL). The histology consistently
showed eosinophilic spongiosis, but the diagnosis of bullous pemphigoid was
only confirmed after 13 years by repeated immunofluorescence studies. The
occurrence of subepidermal blistering diseases in association with B-cell l
ymphoproliferative disorders is rare; a recent study showed that the majori
ty of these cases are epidermolysis bullosa acquisita, confirmed by immunol
ogical studies. Only two cases of immunofluorescence-proven bullous pemphig
oid in association with CLL have been previously reported.