Therapy of Waldenström’s Benign Hypergammaglobulinaemia by Regular Plasmapheresis

Abstract
A patient with a 20-year history of Waldenström’s hypergammaglobulinaemic purpura has over that time developed increasingly troublesome clinical symptoms of purpura and joint swelling, associated with a progressive increase in the level of polyclonal IgG. These symptoms have been controlled by the use of a regular plasmapheresis regime and associated with a reduction in IgG level.

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